Skip to main content

Analysis of knockout mice suggests a role for VGF in the control of fat storage and energy expenditure



Previous studies of mixed background mice have demonstrated that targeted deletion of Vgf produces a lean, hypermetabolic mouse that is resistant to diet-, lesion-, and genetically-induced obesity. To investigate potential mechanism(s) and site(s) of action of VGF, a neuronal and endocrine secreted protein and neuropeptide precursor, we further analyzed the metabolic phenotypes of two independent VGF knockout lines on C57Bl6 backgrounds.


Unlike hyperactive VGF knockout mice on a mixed C57Bl6-129/SvJ background, homozygous mutant mice on a C57Bl6 background were hypermetabolic with similar locomotor activity levels to Vgf+/Vgf+ mice, during day and night cycles, indicating that mechanism(s) other than hyperactivity were responsible for their increased energy expenditure. In Vgf-/Vgf- knockout mice, morphological analysis of brown and white adipose tissues (BAT and WAT) indicated decreased fat storage in both tissues, and decreased adipocyte perimeter and area in WAT. Changes in gene expression measured by real-time RT-PCR were consistent with increased fatty acid oxidation and uptake in BAT, and increased lipolysis, decreased lipogenesis, and brown adipocyte differentiation in WAT, suggesting that increased sympathetic nervous system activity in Vgf-/Vgf- mice may be associated with or responsible for alterations in energy expenditure and fat storage. In addition, uncoupling protein 1 (UCP1) and UCP2 protein levels, mitochondrial number, and mitochondrial cristae density were upregulated in Vgf-/Vgf- BAT. Using immunohistochemical and histochemical techniques, we detected VGF in nerve fibers innervating BAT and Vgf promoter-driven reporter expression in cervical and thoracic spinal ganglia that project to and innervate the chest wall and tissues including BAT. Moreover, VGF peptide levels were quantified by radioimmunoassay in BAT, and were found to be down-regulated by a high fat diet. Lastly, despite being hypermetabolic, VGF knockout mice were cold intolerant.


We propose that VGF and/or VGF-derived peptides modulate sympathetic outflow pathways to regulate fat storage and energy expenditure.


The sympathetic nervous system (SNS) plays an important role in the regulation of glucose and fat metabolism, and its dysfunction could predispose to obesity and type 2 diabetes mellitus. Mice with defective signaling in the melanocortin pathway, including those that fail to express the hypothalamic melanocortin 4 receptor (MC4R) or its agonist alpha-melanocyte stimulating hormone (α-MSH), and those that over-express the MC4R antagonists agouti or agouti-related protein (AGRP or ART), all develop late onset obesity and insulin resistance [1]. The MC4R is expressed in the hypothalamic paraventricular nucleus (PVN), which contains neurons that innervate parasympathetic and sympathetic preganglionic cells in the brainstem and spinal cord, and throughout the brain in sympathetic circuits that innervate brown adipose tissue (BAT) [2, 3]. These projections give the hypothalamus direct input to the autonomic nervous system, controlling glucose and energy homeostasis [4, 5]. The central melanocortin system has therefore been proposed to modulate autonomic outflow and food intake [6, 7] through its effects on sympathetic activity to inhibit pancreatic insulin secretion and increase energy utilization [8, 9].

Brown and white adipose tissues (BAT and WAT) are sites where humoral factors (e.g. leptin and adiponectin) are synthesized and afferent nerve signals generated, which together convey the state of energy storage to the hypothalamus. These signals contribute to the adaptive responses that occur following changes in the environment, including diet and cold. BAT is the primary site of thermogenesis in rodents and newborn humans, is richly innervated by the SNS, and adipocytes are densely packed with mitochondria that contribute to energy generation and heat dissipation. The thermogenic capacity of BAT is primarily due to uncoupling protein 1 (UCP1) on the inner mitochondrial membrane that uncouples the respiratory chain from ATP generation, producing heat [10]. Norepineprine (NE), released from sympathetic nerve endings, stimulates lipolysis in WAT and increases UCP1 gene expression in BAT; these responses to a high fat diet or cold exposure are controlled at least in part by the central melanocortin system [3, 11]. Increased UCP1 expression in WAT, the result of SNS stimulation or genetic background, is associated with brown adipocyte induction in WAT depots, and leads to reversal of diet-induced and genetic obesity [1216]. Taken together, these data argue for an important role of the SNS in the control of energy expenditure via outflow to both white and brown adipose tissues.

We have previously reported suppression of obesity, hyperinsulinemia and hyperglycemia in Ay/a agouti and melanocortin 4 receptor deficient (MC4R-/MC4R-) mice by targeted deletion of the Vgf gene [17, 18]. VGF is a secreted protein and peptide precursor that is expressed throughout the brain, in neurons, and in several neuroendocrine and endocrine tissues [19, 20]. Mice with a targeted deletion of Vgf are lean and hypermetabolic, and resist developing obesity and diabetes [21]. Neonatal treatment of Vgf-/Vgf- mice with monosodium glutamate, which damages the hypothalamus and the hypothalamic projections to the autonomic nervous system [2224], blocks the development of the lean phenotype [17, 18]. This suggests that VGF could regulate energy balance by reducing sympathetic outflow pathway activity to peripheral tissues. To gain insight into the molecular and cellular changes that may be responsible for the increase in energy expenditure and decrease in adipose stores detected in VGF knockout mice, we examined the effect that targeted ablation of VGF has on the regulation of gene expression in adipose tissues, analyzing two independent VGF knockout mouse lines on C57Bl6 backgrounds. We noted alterations in the expression of genes encoding enzymes that control fat synthesis and breakdown, consistent with increased SNS activity. We further found that VGF was expressed in neural pathways innervating BAT, quantified VGF-derived peptides in BAT by RIA, and demonstrated increased UCP1 and UCP2 levels in VGF knockout BAT that were associated with alterations in mitochondrial number and morphology. Our studies support the hypothesis that VGF modulates sympathetic outflow pathway activity to control fat storage and energy expenditure.


Metabolic rates are higher, fat and lean body mass lower, and activity levels similar in Vgf-/Vgf- compared to Vgf+/Vgf+ mice on a C57Bl6 background

Previous studies of VGF knockout mice on a mixed C57Bl6-129/SvJ background (designated VGFMixed knockout and abbreviated VGFM knockout or Vgf M -/-) indicated that mice with the Vgf gene ablated were hyperactive and hypermetabolic. To investigate whether background strain had an effect on metabolic phenotype, we analyzed the same line of VGF knockout mice that had been backcrossed ≥ 10 generations to obtain a homogeneous C57Bl6 background (designated VGFC57 knockout or VgfC 57-/-), as well as the F3 generation of an independent mouse line, generated by Regeneron Pharmaceuticals Inc. using F1H4 ES cells (a 129B6/F1-derived cell line), also primarily on a C57Bl6 background (>83% C57Bl6 background; designated VGFR knockout or Vgf R -/-) [25]. Similar results were obtained using both of these VGF mutant mouse lines on C57Bl6 backgrounds. As shown in Figure 1, metabolic rates remained high in homozygous VGFR knockout mice, with basal metabolic rate (BMR), defined as oxygen consumption (V02) during the light rest period, significantly elevated (p < 0.001; two tailed t-test) in VGF null compared to wild-type littermates. Locomotor activity levels and food intake were indistinguishable between control mice and either VGFR (Figure 1) or VGFC57 (data not shown) knockout mice. Body weight and length were reduced in VGFR and VGFC57 knockout mice [Figure 2 and [18], respectively], and body mass analysis indicated a reduction in fat and lean mass (Figure 2A-C). Consistent with reduced fat and lean mass, low leptin levels, and the hypothesized increase in sympathetic tone in VGF mutant mice, significant reductions in both bone density and bone mineralization were also noted in VGFR knockout mice (Figure 2E-F). Serum chemistries revealed significant reductions in HDL, triglyceride, albumin, and leptin in VGFR knockout mice, while total cholesterol, total protein, insulin, LDL, creatinine, magnesium, urea, and uric acid were not significantly different between knockout and wild type mice on the C57Bl6 background (Table 1).

Table 1 Serum measures in wild type (Vgf R +/+) and VGF knockout (Vgf R -/-) mice.
Figure 1

VGF-deficient mice on a C57Bl6 background are hypermetabolic, with normal food intake and locomotor activity. Metabolic cage analysis revealed that Vgf R -/- mice have significantly increased O2 (V02, panel A) and CO2 (VCO2, panel B) consumption (two-tailed t-test; p ≤ 0.05), while respiratory quotient (panel C), food intake (panels D and E) and locomotor activity (panel F) were similar to wild type littermates (n = 7-8 mice of each genotype). Alternating white and grey shaded regions in panels E-F represent light rest and dark active periods, respectively.

Figure 2

VGF-deficient mice on a C57Bl6 background have decreased fat and lean body mass, and decreased bone mineral density and content. Body weight (Panel A) (grams), body composition (Panels B and C) [lean mass (LM) and fat mass (FM)] (grams), length (Panel D) (cm), bone mineral density (BMD) (Panel E) (g/cm2) and bone mineral content (BMC) (Panel F) (grams), were determined in VGFR mice using dual emission x-ray absorption. Data are expressed as mean ± SEM (n = 7-8 male mice of each genotype per group).

Morphological changes in BAT and WAT of homozygous VGF mutant mice suggest an increase in lipolysis and FA oxidation

Histological examinations of adipose tissues in Vgf -/- and wild type mice were performed to gain insight into which tissues may be responsible for increased energy expenditure and/or decreased fat stores. We compared tissues from Vgf R -/-, -/+, and +/+ mice, although previous studies have not demonstrated significant metabolic differences between wild type and heterozygous VGF knockout mice [17, 18, 21]. Because fat mass is significantly reduced in VgfC 57and Vgf R -/- mice (e.g. Figure 2), certain fat depots were extremely difficult to identify and quantify on the C57Bl6 background, including visceral mesenteric fat, subcutaneous abdominal fat, and retroperitoneal fat. Even though these various fat depots are differentially responsive to a number of stimuli (e.g. diet), and are thought to make specific contributions to glucose and metabolic homeostasis [26], we chose to focus on epididymal WAT and interscapular BAT pads for histological and gene expression analyses because they could be reproducibly isolated from knockout mice. BAT and WAT have distinct physiological roles in maintaining energy homeostasis; BAT is the most highly metabolic and innervated tissue in rodents, while WAT is the principal site of adipose storage. The BAT of VgfC 57-/-, Vgf R -/-, Vgf R +/-, and wild type mice was comprised of typical multilocular cells, however, these cells in VGF knockout mice contained large numbers of smaller lipid droplets, suggesting that the tissue remained metabolically active (Figure 3D-F; quantification panel G; Additional file 1: Supplemental Figure 1). Moreover, the WAT depot that normally surrounds BAT in wild type mice was absent in Vgf -/- mice (see Additional files 1 and 2: Supplemental Figures 1 and 2). WAT from Vgf -/- mice contained less stored lipid in comparison to wild type mice (Figure 3, C and 3A), consistent with the body composition fat mass analysis (Figure 2). Morphometric analysis indicated that mean adipocyte area was significantly reduced in knockout WAT (Figure 3H), which was associated with a shift in the distribution of adipocytes favoring those with smaller perimeters (Figure 3I). In general, quantitative analysis of WAT and BAT demonstrated that heterozygous VGFR knockout mice had an intermediate phenotype between wild type and homozygous knockout mice (Figure 3G and 3H). Overall, H&E analysis of VgfC 57-/- BAT and WAT (Additional file 1: Supplemental Figure 1) revealed a similar pattern of histological staining to that obtained with the respective Vgf R -/- tissues (Figure 3).

Figure 3

Lipid deposition in multilocular cells of brown adipose tissue (BAT) and unilocular cells of white adipose tissue (WAT) is reduced in VGF knockout mice. Representative sections of epididymal WAT (A-C) and interscapular BAT (D-F) from ad lib-fed, age-matched Vgf R +/+ (A, D), +/- (B, E) and -/- (C, F) were stained with H&E. Adipocytes in interscapular BAT and epididymal WAT from -/- mice (C and F) contain less lipid accumulation than the corresponding adipocytes from wild type mice (A and D). Scale bars are 50 μm in length. Morphometric analysis of adipose tissue from Vgf R +/+, +/-, and -/- mice was carried out using MetaMorph, as detailed in Materials and Methods. Lipid area in BAT (panel G), cell area in WAT (panel H), and the distribution of adipocyte perimeters in WAT (panel I), were quantified for each genotype. Note the significant reduction in lipid area in both +/- and -/- BAT (ANOVA, F (2,15) = 73.5, p < 0.0001), significant reduction in adipocyte area in -/- WAT (ANOVA, F (2,15) = 7.6, p = 0.005), and shift in the distribution of cells favoring those with significantly smaller perimeters in -/- and +/- WAT (comparison of mean perimeters in μm; ANOVA, F (2,1167) = 166, p < 0.0001), compared to wild type. Values are mean ± SEM, *p < 0.05, **p = 0.005, ***p < 0.0001 compared to wild type (ANOVA and Bonferroni's posthoc test).

Vgf-/Vgf- mice have altered adipose mRNA levels encoding proteins involved in the regulation of energy storage, fatty acid utilization, and sympathetic nervous system activity

The adipose tissues of VGFC57 and VGFR mutant mice were morphologically different from wild type mice. To understand the molecular mechanisms responsible for decreased fat stores in epididymal WAT and interscapular BAT, we carried out an extensive analysis of gene expression in these VGFC57 tissues using real-time RT-PCR. In WAT, the levels of mRNAs, encoding enzymes responsible for building fat stores, acetyl coA carboxylase (ACC), glycerol-3-phosphate acyltransferse (GPAT) and diacylglycerol acyltransferase (DGAT), were unaltered in Vgf -/- mice, while an increase in mRNA levels encoding hormone sensitive lipase (HSL), an enzyme responsible for lipolysis which mobilizes fat, was found in Vgf -/- mice. Gene expression of peroxisome-proliferator activated receptor gamma (PPARγ), a protein that promotes adipocyte differentiation, and sterol regulatory element binding protein 1C (SREBP-C1), which activates genes responsible for lipogenesis and glucose utilization [27], were decreased in VGF knockout WAT. RNA levels encoding fatty acid synthase (FAS), an enzyme that synthesizes fatty acids from acetyl COA and malonyl COA, however, was elevated in Vgf -/- WAT. In VGF knockout BAT, levels of mRNAs encoding the lipogenic proteins ACC, GPAT and PPARγ were increased (Table 2).

Table 2 Expression of genes in epididymal WAT and interscapular BAT that contribute to lipolysis or lipogenesis in VGF knockout and wild type mice.

Next we looked at gene products responsible for fatty acid beta-oxidation in these tissues. RNA levels of proteins responsible for fatty acid and glucose uptake, lipoprotein lipase (LPL) and glucose 4 transporter (GLUT 4), and translocation of fatty acids to the mitochondria, carnitine palmitoyltransferase 1 (CPT1), were up regulated in Vgf -/- BAT, whereas LPL and GLUT4 gene expression were down regulated and CPT1 mRNA levels unaltered in WAT. PPARα is thought to play an important role in lipid metabolism, and mRNA levels were increased in VGF knockout BAT and WAT. Furthermore, mRNA levels encoding PPARγ coactivator 1 (PGC-1), a co-activator of nuclear receptors that increases metabolism by stimulating mitochondrial biogenesis and respiration, were up-regulated in BAT and WAT of the VgfC 57-/- mutant mouse, and a concomitant increase in cytochrome C oxidase II (COX II) mRNA levels was also found (Table 3).

Table 3 Expression of genes in epididymal WAT and interscapular BAT that contribute to fatty acid oxidation in VGF knockout and wild type mice.

We then investigated whether altered BAT morphology could be associated with an increase in thermogenesis by examining mRNA levels for the uncoupling proteins. Uncoupling Protein 1 (UCP1) by disrupting the proton gradient across the inner mitochondrial membrane is crucial for non-shivering thermogenesis, leading to heat production (reviewed in [2830]). UCP2 and UCP3 also regulate proton conductance, however they require activation by reactive oxygen species, and may protect against oxidative damage (reviewed in [2830]). In addition, UCP3 may transport fatty acids, while UCP2 may attenuate insulin secretion in pancreatic beta cells. In VGFC57 knockout mice compared to wild type mice, we noted that mRNA levels of UCP1 were lower in BAT, but the mRNA levels of UCP2 and UCP3 were increased (Table 4). Notably, in WAT, levels of UCP1 mRNA were robustly increased in Vgf -/- mice (Table 4).

Table 4 Expression of genes in epididymal WAT and interscapular BAT that contribute to thermogenesis in VGF knockout and wild type mice.

Lastly, we looked at genes indicative of sympathetic nervous system (SNS) activity. The SNS-mediated physiological responses, FA oxidation and lipolysis, mostly rely on release of norepinephrine from the post-ganglionic neurons which binds to beta-3-adrenergic receptors (β3AR) on the adipocyte's cell surface, as well as to the other beta receptors, β1AR and β2AR. Mice with decreased sympathetic activity due to leptin deficiency have a ~300-fold reduction in β3AR mRNA in comparison to lean animals [31, 32]. Therefore we looked at the mRNA levels of the beta-adrenergic receptors to provide indirect support for an increase in SNS tone in VGF mutant mice. In BAT, β3AR mRNAs were increased in VGF knockout mice in comparison to wild type mice. In WAT, however, the gene expression of β2AR was significantly higher in Vgf -/- mice than Vgf +/+ mice, while β3AR mRNA levels were similar (Table 5).

Table 5 Expression of genes in epididymal WAT and interscapular BAT that contribute to sympathetic nervous system activity in VGF knockout and wild type mice.

Western and electron microscopic analyses indicate that UCP1 and UCP2 protein levels and mitochondrial number are upregulated in VGF knockout BAT

To determine the basis of the hypermetabolic state in VGF knockout mice, given the somewhat surprising lack of an increase in UCP1 mRNA levels in BAT (Table 4), we examined protein levels of UCPs in BAT by western analysis, and quantified mitochondrial size and number, and cristae density, by electron microscopy. UCP1 and UCP2 protein levels were significantly increased in BAT from Vgf R -/- knockout compared to wild type mice (Figure 4, panels A and B; p < 0.05, ANOVA). To determine whether mitochondrial biogenesis could be affected by germline Vgf ablation, knockout and wild type BAT was examined by electron microscopy (Figure 4, panels C-E and F-H, respectively). Mitochondrial number was increased (Figure 4I), mitochondrial area decreased (Figure 4J), and cristae density increased (Figure 4K), in VGF -/- knockout compared to +/+ wild type mice.

Figure 4

VGF ablation affects UCP1 & UCP2 protein expression, mitochondrial morphology, and mitochondrial number in BAT. Representative western blots of UCP1, UCP2, and GAPDH protein levels in BAT from Vgf R +/+, +/-, and -/- mice (panel A), and densitometric quantification by NIH image (panel B). Comparable results were found in at least three additional experiments. Ablation of VGF significantly increased UCP1 and UCP2 levels in BAT from Vgf R -/- but not Vgf R +/- mice compared to wild type +/+ mice [n = 5 mice per group, mean ± SEM, F (2,12) = 4.35 (UCP1), F (2,12) = 3.33 (UCP2), *p < 0.05, ANOVA and Dunnett's posthoc test]. Representative electron microscope photomicrographs of BAT from Vgf R -/- (panels C-E) and +/+ mice (panels F-H) are shown. The part of the image that is boxed in red is shown at higher magnification in the panel to its immediate right. Scale bars are 5 μm (panels C and F), 2.5 μm (panels D and G), and 1.25 μm (panels E and H). Note that mitochondria are smaller and more numerous in Vgf R -/- in comparison to +/+ BAT (compare panels E and H), which is quantified in panels I and J. In panel K, the number of cristae per μm2 of mitochondrial area was quantified in Vgf R -/- and +/+ BAT. Values are mean ± SEM; ***p = 0.0002 (panel E), **p = 0.001 (panel F), ***p < 0.0001 (panel G) (Student's t-test).

VGF immunoreactivity can be detected in BAT and VGF-derived AQEE30 peptide levels are regulated by diet

BAT is a highly metabolic tissue that is innervated by noradrenergic sympathetic fibers, which also contain other neuropeptides such as NPY [3337]. As previous studies suggested that VGF ablation could potentially impact sympathetic nervous system activity to peripheral metabolic tissues such as fat, and for technical reasons immunohistochemical visualization of VGF in WAT was difficult, we investigated whether VGF was expressed in nerve fibers that innervate BAT. We first quantified the level of VGF-derived C-terminal peptides by subjecting acid extracts of BAT to a sensitive radioimmunoassay (RIA) that has been previously described [38]. This RIA utilizes a polyclonal antibody specific for the VGF-derived C-terminal peptide AQEE30 (VGF peptides are designated by the four N-terminal amino acids and length), so detects AQEE30 and the N-terminally extended peptides that contain this sequence, TLQP62 and NAPP129 [38]. Immunoreactive AQEE30 was detected in BAT, and was found to be downregulated when C57Bl6 mice were fed a high fat diet for two weeks (Figure 5A). Parenchymal nerve fibers make direct contact with adipocytes, activating them via beta-adrenergic receptors, or are associated with finely branched vessels that penetrate the tissue but do not make direct contacts with the adipocytes [39, 40]. By immunofluorescence and immunohistochemistry, anti-VGF staining was found in BAT to abut adipocytes and was also seen in the periarterial plexus (Additional file 3: Supplemental Figure 3, panels A, C, D), similar to the distribution reported for anti-tyrosine hydroxylase (Additional file 3: Supplemental Figure 3, panel B), which binds the rate-limiting enzyme in catecholamine biosynthesis and is a marker of catecholaminergic nerves and terminals [37]. Consistent with finding VGF in nerve fibers and terminals that innervate BAT, we were also able to indirectly localize Vgf gene expression in spinal ganglia and intercostal nerves of heterozygous knockout mice. Intercostal nerves, which contain autonomic and sensory fibers that innervate BAT [41] and additional structures including the skin and musculature of the chest and abdomen, and the dorsal root ganglia, which give rise to the somatic and sensory afferents in the intercostal nerve, were found to express β-galactosidase from the lacZ reporter gene that was knocked into the mouse Vgf locus in Vgf+/Vgf-lacZmice (Figure 5, panels B-C). These initial data suggest that VGF and/or VGF-derived peptides could be released from neurons that innervate adipose tissues, as is NPY [4244], and that VGF AQEE30 peptide levels in BAT are regulated by diet; additional studies will be required to determine whether adipocytes synthesize VGF, analogous to recent reports that they produce NPY [45, 46].

Figure 5

VGF is expressed in neural pathways that innervate brown adipose tissue (BAT). In panel A, levels of VGF-derived peptides were quantified in BAT from C57Bl6 female mice fed standard chow or a high fat, high carbohydrate diet for 14 days. BAT was removed and RIA analysis carried out to quantify C-terminal VGF-derived peptides (NAPP129, TLQP62 and AQEE30, but not full length VGF), using polyclonal anti-AQEE30 (VGF588-617) antiserum as previously described [38]. VGF peptide levels in BAT were significantly reduced in mice fed the high-energy diet in comparison to control mice (p < 0.05). Comparisons by ANOVA [mean ± SEM; high fat diet (n = 4), standard diet (n = 3)]. In panels B-C, Vgf gene expression was visualized in neural pathways that innervate tissues including BAT using a lacZ reporter gene that was knocked into the mouse Vgf locus in VGFR mice (see Methods). In panel B, β-galactosidase expression (blue staining) in the dorsal root ganglia (white arrows) and intercostal nerve (black arrow) is seen in a whole mount preparation from a heterozygous Vgf R +/- mouse. A dorsal root ganglion section is shown at higher magnification in panel C (scale bar is 100 μm in length).

VGF knockout mice are extremely sensitive to acute cold stress

In rodents, the principal functions of BAT are to generate heat during cold exposure so as to maintain body temperature (cold-induced thermogenesis), and to dissipate excess energy in response to dietary intake (diet-induced thermogenesis). To determine whether VGF ablation affected BAT function and thermogenesis, VgfC 57-/- and VgfC 57+/+ mice were acutely exposed to the cold. In contrast to wild type mice that were able to maintain body temperature, VGF knockout mice despite being hypermetabolic rapidly became hypothermic at 4°C (Figure 6).

Figure 6

VGF-deficient mice have increased sensitivity to cold exposure. VgfC 57-/- and VgfC 57+/+ mice were placed at 4°C for 2 hours and allowed ad lib access to food and water. Mice were individually housed and rectal temperatures were taken every 30 minutes. Body temperatures that are marked with an asterix from mutant (n = 2) and wild-type mice (n = 5) are significantly different from each other (ANOVA; p < 0.05; mean ± SEM).


In this study, we investigated the effect that targeted ablation of VGF has on peripheral adiposity, and the possible mechanism(s) by which this neuronal, endocrine, and neuroendocrine secreted polypeptide might regulate fat storage and autonomic homeostasis. VGF mutant mice on a C57Bl6 background are hypermetabolic and lean, with reduced lean and fat mass, despite normal food consumption and locomotor activity levels (Figures 1 and 2). These current findings are consistent with previous studies of VGF mutant mice on a mixed C57Bl6/sv129 background [21]. Thus, serum chemistries, insulin-tolerance, glucose-tolerance, metabolic measurements, and body composition are all very similar among VGF knockout mice on mixed (designated VGFM), homogeneous C57Bl6 (designated VGFC57), or ~83% C57Bl6 backgrounds (designated VGFR) [17, 18] and this report], with the notable exception that VGF knockout mice on a C57Bl6 background (VGFR and VGFC57) are not hyperactive (Figure 1 and data not shown), and thus locomotor activity cannot play a substantive role in their increased energy expenditure.

Could increased sympathetic tone or sensitivity to norepinephrine be responsible for alterations in adipose morphology and the expression of critical gene products? Decreased lipid accumulation in WAT, smaller interscapular WAT depots that are associated with BAT, and regions of fat accretion in BAT, are consistent with increased sympathetic nervous system activity. In addition, changes in gene expression in WAT and BAT correlate with these morphological differences, as does body composition analysis. Activation of the sympathetic nervous system promotes catabolism by increasing glucose and fatty acid uptake into BAT [47], and by increasing lipolysis in WAT. Hormone sensitive lipase (HSL) is induced by sympathetic activity [48], is up-regulated by fasting in most adipose depots except subcutaneous fat [4951], and both HSL mRNA and protein levels in adipose tissue are decreased in the obese insulin-resistant state [52]. Of note, HSL was one of the most robustly up-regulated genes in WAT from VgfC57 -/- mice (Table 2). Although lipoprotein lipase (LPL) activity is generally regulated at the post-transcriptional level in adipose tissues (e.g. [53]), allowing rapid responses to alterations in diet, LPL mRNA levels correlate with PPARγ mRNA levels in epididymal WAT [54] and increase with PPARγ agonist treatment [55], likely due to a transcriptionally active PPAR response element upstream of the LPL gene [56]. Small but significant decreases in LPL mRNA and PPARγ mRNAs were noted in WAT from VGF knockout mice, while small increases in both mRNA levels were measured in BAT. Increased LPL expression in BAT has previously been described in mice exposed to cold or injected with norepinephrine [57], so the increased LPL expression we measured in VGFC57 knockout BAT may reflect increased sympathetic pathway activity. Decreased fat stores could result from continuous breakdown of triglycerides into fatty acids, which is associated with increased fatty acid synthase (FAS) mRNA levels in WAT and higher circulating FFA levels previously noted in Vgf-/Vgf- mice on a C57Bl6 background [18]. We further noted increases in cytochrome c oxidase II, PPARα, PGC1, UCP1, and UCP2 mRNA levels in WAT from VGF knockout mice. The PGC1 coactivators play essential roles in BAT differentiation, mitochondrial biogenesis, and thermogenesis [58], so increased expression of PGC1 could drive alterations in WAT morphology and UCP1 gene expression towards a 'brown fat' phenotype in VgfC 57-/- mice.

Previous studies indicate that induction of UCP1 levels in the absence of increased adrenergic activity does not necessarily lead to increased UCP1 activity and thermogenesis [59, 60]. Conversely, the thermogenic capacity of BAT can be augmented without an associated increase in sympathetic activity, as noted in the Syrian hamster exposed to a short photoperiod or fed a high-energy diet, where increased thermogenesis occurs in the absence of changes in norepinephrine turnover [6163]. Our metabolic studies of VGF mutant mice consistently demonstrate increased O2 consumption irrespective of genetic background ([21] and this report), and together with the current analysis of gene expression, would be most consistent with increased fatty acid oxidation and decreased lipogenesis in adipose tissues, and possibly also thermogenic activity due to enhanced UCP1 levels in WAT, which could be associated with increased adrenergic activity. In BAT, targeted ablation of VGF resulted in increased UCP1 protein levels, increased mitochondrial number, and increased cristae number per square micron of mitochondrial area, suggesting increased sympathetic activity, but did not increase cold tolerance. Cold intolerance (Figure 6) in VGF mutants could be a result of lack of available fuel, as in the ad lib fed state, these mice have reduced fat depots and display a fasted phenotype, with little detectable liver glycogen, low circulating glucose levels, increased circulating FFA, elevated hypothalamic NPY and AGRP mRNA levels, and decreased hypothalamic POMC mRNA levels [17, 18, 21]. Alternatively, sympathetic outflow to various adipose depots could differ, as has been demonstrated for specific WAT pads during prolonged fasting and following leptin administration [64, 65].

Neonatal monosodium glutamate (MSG) blocks the development of the lean phenotype in VGFM knockout mice [17], suggesting that increased SNS activity is associated with increased fat oxidation and energy expenditure in homozygous Vgf-/Vgf- mice. Neonatal guanethidine treatment, which creates a generalized chemical sympathectomy, also blocked the development of the lean phenotype in VGFC57 knockout mice, and increased circulating glucose levels (see Additional file 2: Supplemental Figure 2), but was not sufficiently well-tolerated by VGF knockout mice to carry out a complete analysis of its effects. These experiments are consistent with the real-time PCR data, and a role for increased sympathetic pathway activity in mice that lack VGF. Although we were unable to study the developing SNS in Vgf-/Vgf- P0 newborn pups due to insufficient numbers, we did note that tyrosine hydroxylase (TH) immunostaining in the SNS of VgfC 57+/- pups was significantly more robust than VgfC 57+/+ pups, consistent with a possible increase in SNS catecholamine turnover (E. Watson and S. Salton, unpublished data) [66]. Increased sympathetic tone in the absence of changes in BAT UCP1 gene expression was noted in lean, hypermetabolic M3 muscarinic acetylcholine receptor knockout mice [67], which are very similar to VGF mutant mice in phenotype, and also largely resistant to high fat diet-induced, gold-thio-glucose-induced and genetically (ob/ob)-induced obesity, hyperphagia, hyperinsulinemia, and hyperglycemia [17, 18, 21, 67].

Both cold exposure and overeating increase sympathetic drive to BAT to stimulate thermogenesis [6870]. Are the sympathetic pathways that control increased energy expenditure and decreased fat storage regulated by independent CNS circuits? Adipose-synthesized leptin controls energy balance in part via activation of the SNS [71], regulating body weight and temperature [7274]; chemical sympathectomy with guanethidine blocks this leptin effect, preventing diet-induced thermogenesis [75]. Leptin regulates functionally divergent hypothalamic MC4R-containing pathways to control food intake and energy expenditure [76]. MC4R mRNA has also been localized in sympathetic nervous system outflow neurons that innervate WAT [2]. How the CNS and sympathetic outflow circuits coordinately regulate lipid mobilization in WAT and thermogenesis in BAT in response to cold stress and/or diet is not fully understood, but retrograde tract tracing with pseudorabies virus suggests that MC4R-expressing cells in the hypothalamic PVN are positioned to increase sympathetic drive to both WAT and BAT [2]. It is likely, however, that both melanocortin and melanocortin-independent pathways are involved, as MC4R-deficient mice are still able to maintain normal body temperature and thermo-regulate during extended cold exposure [77], but are apparently unable to up-regulate UCP1 in BAT in response to short term cold stress or a high fat diet [3]. VGF ablation blocks obesity, hyperglycemia and hyperinsulinemia in MC4R-deficient mice [18], so this protein may function in these outflow pathways to regulate sympathetic nervous system activity and lipid storage.

Adaptive thermogenesis is mediated primarily via beta-adrenergic receptors, and genetic association studies have revealed that the genes encoding these receptors include a large number of coding and non-coding polymorphisms, which have clear functional consequences but less clear contributions to the pathogenesis of obesity, diabetes and hypertension [78]. Mice that lack β1, β2 and β3 adrenergic receptors ('beta-less' mice) are obese, primarily the result of defective SNS-dependent activation of diet-induced thermogenesis because lipolytic responses to fasting were not altered [79, 80]. Siberian hamsters have an increase in sympathetic drive during short day exposure, which reduces fat mass [81, 82]. This increase in SNS activity correlates with an increase in β3 receptor mRNA levels in adipose tissues [82], and interestingly, we noted an increase in β3 receptor mRNA levels in VGF knockout BAT but not WAT, and increased β2 receptor mRNA levels in WAT, perhaps correlating with increased SNS activity [79]. Recent studies indicate that norepinephrine can induce lipolysis in WAT in beta-less mice [83], suggesting a beta-adrenoreceptor independent pathway, and moreover, in the absence of norepinephrine or epinephrine, dopamine-beta-hydroxylase (DBH) knockout mice are not predisposed to obesity, as are beta-less mice, and maintain glucose tolerance [84]. The contribution of beta-adrenoreceptors and SNS activity to fat mass is therefore complicated, and notably, leptin-induced decreases in fat mass are not consistently accompanied by increases in norepinephrine (NE) turnover, a measure of SNS activity [65]. Further studies are needed to investigate whether increased HSL gene expression and lipolysis are associated with increased NE turnover in specific fat depots from VGF mutant mice.

Of note, the neuropeptides α-MSH and NPY have been demonstrated to increase and decrease lipolysis, respectively, in fully differentiated 3T3-L1 adipocytes [42], so by analogy, direct effects of VGF peptides on adipocytes are also possible, particularly in light of the expression of VGF in BAT (Figure 5) and in the sympathetic nervous system [85, 86]. We quantified AQEE immunoreactive peptides by RIA in BAT, and noted that levels decrease in response to a high fat diet (HFD). Parallel studies with larger cohorts of C57Bl6 mice have revealed that C57Bl6 mice consuming a HFD compared to a chow diet generally increase their energy intake (food consumption in grams is similar) [87], and after 2 weeks, body weight has not changed [87], or has increased by ~10% ([88]; J. Mastaitis and C.V. Mobbs, personal communication and [89]). This alteration in energy balance is sufficient to trigger compensatory changes in gene expression in liver [87], including increased expression of genes involved in fatty acid oxidation. Our data would suggest that VGF C-terminal peptide TLQP62, hypothesized to decrease sympathetic outflow pathway activity to adipose tissues [17, 18], is present in BAT and levels decrease as part of the compensatory response to increased energy intake.

Recent experiments have found that 14-day intracerebroventricular (icv) administration of the C-terminal VGF-derived peptide TLQP21 (VGF residues 556-576) increases energy expenditure and prevents diet-induced obesity in mice [90], and decreases food intake and body weight in hamsters [91]. Analysis of TLQP21-treated mice revealed a phenotype with numerous additional similarities to VGF knockout mice including increased energy expenditure, increased WAT β2-adrenergic receptor mRNA levels, increased WAT UCP1 mRNA levels, normal locomotor activity, and decreased WAT weight {see Results and [21]}. However, rather than very similar phenotypes, one would anticipate that mice lacking VGF and those chronically treated with VGF-derived TLQP21 peptide would potentially have opposing metabolic phenotypes. Because the precise levels of TLQP21 in brain tissue are not yet known compared to the relatively abundant C-terminal TLQP62 peptide (VGF residues 556-617), one of the major VGF-derived peptides detected in neuronal and endocrine tissues [38, 92, 93], and different C-terminal peptides derived from TLQP62 have opposing effects on energy balance [94], several alternative mechanisms of action are possible: (1) TLQP21 and TLQP62 could each activate its own receptor with the overall biological effect dependent on the concentration of each peptide and the distribution and affinity of putative receptors, (2) TLQP21 could inhibit actions of full length VGF or longer VGF-derived C-terminal peptides, including TLQP62 and NAPP129, which all contain the TLQP21 sequence, and/or (3) chronic TLQP21 treatment could lead to down-regulation of VGF receptor(s) and signaling. Consistent with mechanism 2, we have recently noted that TLQP21, but not a scrambled peptide, blocks TLQP62-induced electrical potentiation in hippocampal slices [95]. In addition, Severini et al. [96] have recently described a role for TLQP21 in cerebellar granule neuron survival and cellular signaling, and in the regulation of gastric motor function [97]. Taken together, these data indicate that specific VGF-derived peptides are biologically active, and may signal through independent or shared cell surface receptor(s) to regulate autonomic homeostasis and peripheral adiposity.


Study of two independent VGF knockout mouse lines indicates that Vgf gene products regulate fat storage and energy expenditure through a mechanism that is independent of an effect on locomotor activity. Histological and electron microscopic analysis, coupled with real-time PCR and western analysis, demonstrate physiological and morphological changes in VGF germline knockout mice that are consistent with decreased fat storage, decreased adipocyte area, increased lipolysis, and decreased lipogenesis in WAT, and increased fatty acid oxidation, increased UCP1 and UCP2 protein levels, and increased mitochondrial number and cristae density in BAT. Identification of VGF in BAT, together with these data, supports the hypothesis that VGF and/or VGF-derived peptides modulate sympathetic outflow pathways that regulate adiposity and energy expenditure.


Mouse Strains and Diets

Previously described mice with a targeted deletion of the Vgf gene on a mixed C57Bl/6 and 129/SVJ background (designated VGFM or Vgf M -/-) [21], were repetitively backcrossed 10 generations onto wild type C57Bl/6 mice (designated VGFC57 or VgfC 57-/-), and heterozygous Vgf+/Vgf- mice on a homogenous C57Bl/6 background were mated to generate wild type, heterozygous, and homozygous VGF-deficient mice. A second VGF-deficient line was generated by Regeneron Pharmaceuticals Inc. as previously described [25] using F1H4 ES cells (a 129B6/F1-derived cell line) and a BAC-based targeting vector with deletion of the entire Vgf coding sequence and insertion of an in frame lacZ reporter gene and neomycin-selection cassette; chimeric mice resulted from the injection of two independent Vgf-/Vgf- embryonic stem cell clones into C57BL6/J blastocysts. Male chimeras were mated with C57BL6/J females to produce F1 breeders and experiments were performed on N2F1 mice (>83% C57Bl6 background; designated VGFR or Vgf R -/-) from two separate clones with similar results.

Mice were housed at room temperature in a 12 h light, 12 h dark cycle, with chow and water available ad lib unless otherwise specified. Mice fed standard chow received a 4.5% fat, 55% carbohydrate, 20% protein, 4.7% fiber diet (Purina PicoLab Rodent Diet 20-5053; 4 Kcal/gm; Purina. St. Louis, MO). For high fat diet studies, mice received a high fat (33.5-35.5%) and high simple carbohydrate (34-35.5%) diet that also contained 20% protein and 0.1% fiber (Bio-Serv F2685; 5.4 kcal/g). All animal studies were conducted in accordance with the Guide for Care and Use of Experimental Animals, using protocols approved by Institutional Animal Care and Use Committees at Mount Sinai School of Medicine or Regeneron Pharmaceuticals Inc.

Tissue Preparation and Immunohistochemistry

Mice were sacrificed and white and brown adipose tissues removed, fixed in formalin and embedded in paraffin. Sections (5 μm) were stained with hemotoxylin and eosin. Transcardial perfusions were performed with 4% paraformaldehyde in PBS after washing in saline solution. After perfusion brown adipose tissue was dissected and fixed overnight in the same fixative and then embedded in paraffin for immunohistochemistry. Polyclonal rabbit antibodies were raised against a VGF (amino acids 8-349)-trpE fusion protein [98]. Dewaxed sections (10 μm) were processed through the following steps for antigen retrieval: (1) treated with 0.3% hydrogen peroxide in methanol for 20 minutes; (2) microwaved for 20 minutes in 10 mM citric acid buffer to retrieve antigens; (3) incubated for 48 hours at 4°C in PBS that contained 0.3% Triton X100, 3% normal goat, 3% horse serum, and anti-VGF or anti-tyrosine hydroxylase (Chemicon International, Temecula, CA) antibody (1:50); (4) incubated for 1 hour in biotinylated secondary antibody, goat anti-rabbit IgG (1:200). Staining was performed using an avidin:biotyinylated enzyme complex (vector ABC kit, Vector laboratories, Burlingame, CA) with diaminobenzidine as a substrate. For immunofluorescence, polyclonal rabbit anti-VGF (1:1000) was used to stain BAT. Dewaxed sections (10 μm) were subjected to an antigen retrieval step, were incubated overnight at 4°C in PBS that contained 0.3% Triton X100, 3% normal goat, 3% horse serum, and VGF antibody (1:50), and lastly with Texas red goat anti-rabbit 1:250 for 1 hour. Staining was visualized using a Zeiss Axiophot microscope.


Isolated BAT and WAT were immersed and fixed in formalin, embedded in paraffin, sectioned, and stained with H&E. Slides were analyzed using Zeiss Axiophot microscope and images captured with a SPOT digital camera. Calculation of mean cell size, lipid area, and cell size distribution was performed using MetaMorph Imaging Software (Molecular Devices, Downingtown, PA). For image analysis, 6 images per group were randomly selected to measure the mean cell size and size distribution in WAT. Groups consisted on 2 mice of each genotype [wild type (Vgf+/Vgf+), heterozygous knockout (Vgf+/Vgf-), and homozygous knockout (Vgf-/Vgf-)], and images were taken with 20× and 10× objectives for BAT and WAT, respectively. Mean cell size and size distribution were determined from 390 adipocytes in WAT. As it was difficult to outline the cells in BAT because of the accumulation of lipid in the cytoplasm, lipid area in BAT was quantified using MetaMorph Imaging Software.

Electron Microscopy

For electron microscopic examination, BAT samples were placed in ice-cold fixative buffer (3% gluteraldehyde in 0.2 M sodium cacodylate buffer pH 7.3) for 2 h. Specimens were washed in 0.2 M sodium cacodylate buffer pH 7.3 for 10 min, postfixed in 1% osmium tetroxide in 0.2 M sodium cacodylate buffer for 1 h, washed and dehydrated in graded ethyl alcohol steps, and embedded in pure EPON A&B mixture with DMP-30. Ultrathin sections for electron microscopy were examined using a Hitachi H7650 instrument linked to an SIA digital camera (Scientific Instruments and Applications, Duluth, GA) controlled by Maxim CCD software. Electron micrographs were obtained at 20,000× magnification, and mitochondrial analysis was carried out using MetaMorph Imaging Software. Six images per group [2 mice of each genotype: wild type (Vgf+/Vgf+) and homozygous knockout (Vgf-/Vgf-)] were randomly chosen, and the number and the area of mitochondria/μm2 were measured. The mean mitochondrial area/μm2 was determined from 316 mitochondria in BAT. The cristea number was calculated from 40 mitochondria for each group (2 images/group).

Western Blot Analysis

BAT and epididymal WAT from wild type (Vgf+/Vgf+), heterozygous knockout (Vgf+/Vgf-), and homozygous knockout (Vgf-/Vgf-) (n = 5 mice for each group) were homogenized in ice cold lysis buffer [50 mM Tris-HCl (pH 8) 150 mM NaCl, 0.02% sodium azide, 0.1% SDS, 0.5% deoxycholate and 1% NP40] supplemented with protease and phosphatase inhibitor cocktails (Roche Diagnostics, Mannheim, Germany; Thermo Scientific, Waltham, MA). Lysates were cleared by centrifugation (14,000 rpm, 10 min at 4°C), and the protein concentration of the supernatant determined by the BCA protein method (Thermo Scientific). Protein samples (25 μg) were separated by SDS-PAGE and transferred to nitrocellulose membranes (Millipore, Bedford, MA). Membranes were blocked with 5% (W/V) BSA in phosphate-buffered saline, and were probed with rabbit polyconal anti-UCP1 [1:1000 (v/v)] (Calbiochem, San Diego CA), rabbit polyconal anti-UCP2 [1:1000 (v/v)] (Calbiochem), or mouse monoclonal anti-GAPDH [1:1000 (v/v)] (Cell Signaling Technology, Danvers, MA), at 4°C overnight. After 3 washes in PBS-T (0.1% Tween in PBS) membranes were incubated for 1 hour with HRP-conjugated secondary antibody [1:10,000 (v/v) in PBS-T] (GE Healthcare, Piscataway, NJ) containing 5% non-fat dry milk. After 3 washes in PBS-T bound antibodies were detected using ECL (Thermo Scientific) and exposure to HyBlot CL (Denville Scientific, Metuchen, NJ). Densitometric quantification was performed using NIH ImageJ.

β-galactosidase Histology

For β-galactosidase staining, mice were deeply anesthetized (240 mg/kg ketamine, 48 mg/kg xylazine i.m.) and exsanguinated with ice-cold heparinized saline. Tissues were fixed by transcardial perfusion of 2% paraformaldehyde in 0.1 M phosphate buffer, postfixed for 2 hr, and then washed in several changes of phosphate-buffered saline. Whole mount staining was then carried out essentially as previously described [99, 100], preparations were examined, and then cryoprotected for a least 24 hr in two changes of buffered 30% sucrose at 4°C with agitation before sectioning.


Tissues were sonicated and extracted in 0.1 M acetic acid for 6-7 min at 70°C [101]. Homogenates were subjected to centrifugation (14,000 × g for 30 min, 4°C), and the supernatants were dried using a Speed Vac concentrator (Sorvall) and stored at -80°C. Samples were resuspended in 0.1 M NaHPO4, 0.1% TritonX-100, pH 7.2 and subjected to RIA. Rabbit polyclonal antiserum directed against the VGF-derived C-terminal AQEE30 peptide was utilized, and RIAs carried out as previously described [38]. Under these acid extraction conditions, the RIA directed against the C-terminal AQEE30 peptide would also be expected to cross-react with N-terminally extended peptides TLQP62 and NAPP129 in these tissue extracts.

RNA isolation and RT-PCR

Mice were sacrificed, and brown and white (epididymal fat pads) adipose tissues were removed, flash frozen on dry ice, and stored at -80°C until use. Fat pads were homogenized in Trizol and RNA was extracted according to the manufacturer's instructions (Invitrogen Corporation, Carlsbad, CA). Total RNA (5 μg) was reverse transcribed in a 20 μl reaction using Superscript II enzyme (Invitrogen Corporation, Carlsbad, CA), and single stranded cDNA was diluted 1:50 for RT-PCR. Using Syber Green Master Mix (Applied Biosystems, Foster City, CA), amplification was performed in ABI Prism 8500 system for 40 cycles in quadruplicate. SDS 2.1 software was used for analyzing cycle threshold (Ct) values, and expression of the housekeeping gene beta actin was used to normalize levels according to the following formula: ΔΔCt = (Ct geneX VGFko - Ct actin VGFko) - (Ct geneX wild type - Ct actin wild type). Fold difference in mRNA levels between Vgf-/Vgf- and Vgf+/Vgf+ = 2ΔΔCt. Forward and reverse primers were designed based on published studies and on database analysis as follows: acetyl-CoA carboxylase (ACC), 5'-CAGATCCAGGCCATGTTGAGACG and 3'-TCGCTGGGTGGGTGAGATGTG; beta-1-adrenergic receptor (β1AR), 5'-CGGCTGCAGACGCTCACCAA and 3'-CGCCACCAGTGCATGAGGAT; beta-2-adrenergic receptor (β2AR), 5'-GCTGCAGAAGATAGACAAAT and 3'-GGGATCCTCACACAGCAGTT; beta-3-adrenergic receptor (β3AR), 5'-CTGCTAGCATCGAGACCTT and 3'-CGAGCATAGACGAAGAGCAT; carnitine palmitoyltransferase 1 (CPT1), 5'-ACCACTGGCCGAATGTCACAA and 3'-AGCGCGTAGCGCATGGTCAT; cytochrome C oxidase II (COX II), 5'-CGATTCCAACTTGGTCTACAA and 3'-GGAACCATTTCTAGGACAATG; diacylglycerol acyltranferase (DGAT), 5'-TCCGCCTCTGGGCATTC and 3'-GAATCGGCCCACAATCCA; fatty acid synthase (FAS), 5'-TGCTCCCAGCTGCAGGC and 3'-GCCCGGTAGCTCTGGGTGTA; glucose-4-transporter (GLUT4), 5'-CTCAGCAGCGAGTGACTGGGAC and 3'-CCCTGAGTAGGCGCCAATGAGG; glycerol-3-phosphate acyltransferase (GPAT), 5'-CAGCTCTGCTGCCATCTTTG and 3'-TGCAGCTTCTGCAGGTACTCA; hormone sensitive lipase (HSL), 5'-GAAAAACAGCCTGTCGGACCA and 3'-CCAGGGCGATCTGCAGGT; insulin receptor (IR), 5'-GTAGCCTGATCATCAACATCCG and 3'-CCTGCCCATCAAACTCTGTCAC; insulin receptor substrate 1 (IRS1), 5'-CCTCTCCAACGCCAGAAGCTGCC and 3'-ATGGCGAGCCCTCCGGATACCG; insulin receptor substrate 2 (IRS2), 5'-GGATAATGGTGACTATACCGAGA and 3'-CTCACATCGATGGCGATATAGTT; lipoprotein lipase (LPL), 5'-AGGACCCCTGAAGACAC and 3'-GGCACCCAACTCTCATA; peroxisome proliferator activated receptor alpha (PPARα), 5'-TCCCTTGTAGCCTTTTGTCAT and 3'-AAGCCATTGCCGTACGCGAT; peroxisome proliferator activated receptor gamma (PPARγ), 5'-AGGCCGAGAAGGAGAAGCTGTTG and 3'-TGGCCACCTCTTTGCTCTGCTC; PPARγ coactivator 1 (PGC-1), 5'-AAAGAATTCGAACTAAGGGATGGCGACTT and 3'-ATAGGATCCGGAATATGGTGATCGGGAAC; sterol regulatory element binding protein 1C (SREBP1C), 5'-GAGGCACTCCCCCAAAAGAT and 3'-TGATGAGAGGGAGGCCATTT; uncoupling protein 1 (UCP1), 5'-GATCCAAGGTGAAGGCCAGG and 3'-GTTGACAAGCTTTCTGTGG; uncoupling protein 2 (UCP2), 5'-GTGACCTGCTGCGCTGTGGTACT and 3'-GATCCAAGGGGAGAGTCA; housekeeping gene (beta actin), 5'-TGCTGTCCCTGTATGCCTCT and 3'-AGGTCTTTACGGATGTCACG

Indirect Calorimetry, Body Composition and Serum Chemistries

Metabolic measurements were assessed on a regular diet (at 9-10 weeks of age) and were obtained using an Oxymax (Columbus Instruments International Corp.) open circuit indirect calorimetry system as previously described [102]. The first 2 h was a period of adaptation for the animals, and metabolic rate (V O2), RQ (ratio of V CO2/V O2) and activity (counts) were then evaluated for a 72-h period. Energy expenditure was calculated as the product of calorific value of oxygen (calorific value of oxygen = 3.815 + 1.232 RQ) and the volume of O2 consumed and this was normalized for body weight in kilograms. Two cohorts of male mice between 2-3 months of age (n = 7-8 mice of each genotype per cohort) were utilized for body composition, serum chemistry and metabolic cage analysis, carried out as described above and detailed previously [103].

Data and Statistical Analysis

Data are expressed as mean ± SEM. Comparisons were performed using t test or repeated-measures analysis of variance (ANOVA) where appropriate, using the programs Statview and Prism. P-values less than 0.05 were considered significant. For metabolic cage analysis, basal metabolic rate (BMR), defined as oxygen consumption during the light rest period, was determined by comparing VO2 measurements of VGFR knockout and wild-type littermates by two-tailed t-test. For real-time RT-PCR, assays were carried out in quadruplicate, and mean cycle threshold (Ct) values (± SEM) were compared by two-way ANOVA (p ≤ 0.05 was considered significant). These values were used to calculate fold difference in mRNA levels (2ΔΔCt).


  1. 1.

    Barsh G: From Agouti to Pomc--100 years of fat blonde mice. Nat Med. 1999, 5 (9): 984-985.

    CAS  PubMed  Article  Google Scholar 

  2. 2.

    Song CK, Jackson RM, Harris RB, Richard D, Bartness TJ: Melanocortin-4 receptor mRNA is expressed in sympathetic nervous system outflow neurons to white adipose tissue. Am J Physiol Regul Integr Comp Physiol. 2005, 289 (5): R1467-1476.

    CAS  PubMed  Article  Google Scholar 

  3. 3.

    Voss-Andreae A, Murphy JG, Ellacott KL, Stuart RC, Nillni EA, Cone RD, Fan W: Role of the central melanocortin circuitry in adaptive thermogenesis of brown adipose tissue. Endocrinology. 2007, 148 (4): 1550-1560.

    CAS  PubMed  Article  Google Scholar 

  4. 4.

    Elmquist JK, Maratos-Flier E, Saper CB, Flier JS: Unraveling the central nervous system pathways underlying responses to leptin. Nat Neurosci. 1998, 1 (6): 445-450.

    CAS  PubMed  Article  Google Scholar 

  5. 5.

    Kishi T, Aschkenasi CJ, Lee CE, Mountjoy KG, Saper CB, Elmquist JK: Expression of melanocortin 4 receptor mRNA in the central nervous system of the rat. J Comp Neurol. 2003, 457 (3): 213-235.

    CAS  PubMed  Article  Google Scholar 

  6. 6.

    Bray GA, York DA: The MONA LISA hypothesis in the time of leptin. Recent Prog Horm Res. 1998, 53: 95-117. discussion 117-118

    CAS  PubMed  Google Scholar 

  7. 7.

    Friedman JM, Halaas JL: Leptin and the regulation of body weight in mammals. Nature. 1998, 395 (6704): 763-770.

    CAS  PubMed  Article  Google Scholar 

  8. 8.

    Fan W, Dinulescu DM, Butler AA, Zhou J, Marks DL, Cone RD: The central melanocortin system can directly regulate serum insulin levels. Endocrinology. 2000, 141 (9): 3072-3079.

    CAS  PubMed  Google Scholar 

  9. 9.

    Li G, Mobbs CV, Scarpace PJ: Central pro-opiomelanocortin gene delivery results in hypophagia, reduced visceral adiposity, and improved insulin sensitivity in genetically obese Zucker rats. Diabetes. 2003, 52 (8): 1951-1957.

    CAS  PubMed  Article  Google Scholar 

  10. 10.

    Ricquier D: Fundamental mechanisms of thermogenesis. C R Biol. 2006, 329 (8): 578-586. discussion 653-575

    CAS  PubMed  Article  Google Scholar 

  11. 11.

    Brito MN, Brito NA, Baro DJ, Song CK, Bartness TJ: Differential activation of the sympathetic innervation of adipose tissues by melanocortin receptor stimulation. Endocrinology. 2007, 148 (11): 5339-5347.

    CAS  PubMed  Article  Google Scholar 

  12. 12.

    Collins S, Daniel KW, Petro AE, Surwit RS: Strain-specific response to beta 3-adrenergic receptor agonist treatment of diet-induced obesity in mice. Endocrinology. 1997, 138 (1): 405-413.

    CAS  PubMed  Google Scholar 

  13. 13.

    Cousin B, Cinti S, Morroni M, Raimbault S, Ricquier D, Penicaud L, Casteilla L: Occurrence of brown adipocytes in rat white adipose tissue: molecular and morphological characterization. J Cell Sci. 1992, 103 (Pt 4): 931-942.

    CAS  PubMed  Google Scholar 

  14. 14.

    Ghorbani M, Himms-Hagen J: Appearance of brown adipocytes in white adipose tissue during CL 316,243-induced reversal of obesity and diabetes in Zucker fa/fa rats. Int J Obes Relat Metab Disord. 1997, 21 (6): 465-475.

    CAS  PubMed  Article  Google Scholar 

  15. 15.

    Guerra C, Koza RA, Yamashita H, Walsh K, Kozak LP: Emergence of brown adipocytes in white fat in mice is under genetic control. Effects on body weight and adiposity. J Clin Invest. 1998, 102 (2): 412-420.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  16. 16.

    Xue B, Coulter A, Rim JS, Koza RA, Kozak LP: Transcriptional synergy and the regulation of Ucp1 during brown adipocyte induction in white fat depots. Mol Cell Biol. 2005, 25 (18): 8311-8322.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  17. 17.

    Hahm S, Fekete C, Mizuno TM, Windsor J, Yan H, Boozer CN, Lee C, Elmquist JK, Lechan RM, Mobbs CV, et al: VGF is required for obesity induced by diet, gold thioglucose treatment and agouti, and is differentially regulated in POMC- and NPY-containing arcuate neurons in response to fasting. J Neurosci. 2002, 22: 6929-6938.

    CAS  PubMed  Google Scholar 

  18. 18.

    Watson E, Hahm S, Mizuno TM, Windsor J, Montgomery C, Scherer PE, Mobbs CV, Salton SR: VGF ablation blocks the development of hyperinsulinemia and hyperglycemia in several mouse models of obesity. Endocrinology. 2005, 146 (12): 5151-5163.

    CAS  PubMed  Article  Google Scholar 

  19. 19.

    Salton SR, Ferri GL, Hahm S, Snyder SE, Wilson AJ, Possenti R, Levi A: VGF: a novel role for this neuronal and neuroendocrine polypeptide in the regulation of energy balance. Front Neuroendocrinol. 2000, 21 (3): 199-219.

    CAS  PubMed  Article  Google Scholar 

  20. 20.

    Levi A, Ferri GL, Watson E, Possenti R, Salton SR: Processing, distribution and function of VGF, a neuronal and endocrine peptide precursor. Cell Mol Neurobiol. 2004, 24: 517-533.

    CAS  PubMed  Article  Google Scholar 

  21. 21.

    Hahm S, Mizuno TM, Wu TJ, Wisor JP, Priest CA, Kozak CA, Boozer CN, Peng B, McEvoy RC, Good P, et al: Targeted deletion of the Vgf gene indicates that the encoded secretory peptide precursor plays a novel role in the regulation of energy balance. Neuron. 1999, 23 (3): 537-548.

    CAS  PubMed  Article  Google Scholar 

  22. 22.

    Bergen HT, Mizuno TM, Taylor J, Mobbs CV: Hyperphagia and weight gain after gold-thioglucose: relation to hypothalamic neuropeptide Y and proopiomelanocortin. Endocrinology. 1998, 139 (11): 4483-4488.

    CAS  PubMed  Google Scholar 

  23. 23.

    Morris MJ, Tortelli CF, Filippis A, Proietto J: Reduced BAT function as a mechanism for obesity in the hypophagic, neuropeptide Y deficient monosodium glutamate-treated rat. Regul Pept. 1998, 75-76: 441-447.

    CAS  PubMed  Article  Google Scholar 

  24. 24.

    Tsukahara F, Uchida Y, Ohba K, Ogawa A, Yoshioka T, Muraki T: The effect of acute cold exposure and norepinephrine on uncoupling protein gene expression in brown adipose tissue of monosodium glutamate- obese mice. Jpn J Pharmacol. 1998, 77 (3): 247-249.

    CAS  PubMed  Article  Google Scholar 

  25. 25.

    Valenzuela DM, Murphy AJ, Frendewey D, Gale NW, Economides AN, Auerbach W, Poueymirou WT, Adams NC, Rojas J, Yasenchak J, et al: High-throughput engineering of the mouse genome coupled with high-resolution expression analysis. Nat Biotechnol. 2003, 21 (6): 652-659.

    CAS  PubMed  Article  Google Scholar 

  26. 26.

    Shi H, Strader AD, Woods SC, Seeley RJ: The effect of fat removal on glucose tolerance is depot specific in male and female mice. Am J Physiol Endocrinol Metab. 2007, 293 (4): E1012-1020.

    CAS  PubMed  Article  Google Scholar 

  27. 27.

    Ferre P, Foufelle F: SREBP-1c Transcription Factor and Lipid Homeostasis: Clinical Perspective. Horm Res. 2007, 68 (2): 72-82.

    CAS  PubMed  Article  Google Scholar 

  28. 28.

    Krauss S, Zhang CY, Lowell BB: The mitochondrial uncoupling-protein homologues. Nat Rev Mol Cell Biol. 2005, 6 (3): 248-261.

    CAS  PubMed  Article  Google Scholar 

  29. 29.

    Affourtit C, Crichton PG, Parker N, Brand MD: Novel uncoupling proteins. Novartis Found Symp. 2007, 287: 70-80. discussion 80-91

    CAS  PubMed  Article  Google Scholar 

  30. 30.

    Echtay KS: Mitochondrial uncoupling proteins--what is their physiological role?. Free Radic Biol Med. 2007, 43 (10): 1351-1371.

    CAS  PubMed  Article  Google Scholar 

  31. 31.

    Collins S, Daniel KW, Rohlfs EM, Ramkumar V, Taylor IL, Gettys TW: Impaired expression and functional activity of the beta 3- and beta 1- adrenergic receptors in adipose tissue of congenitally obese (C57BL/6J ob/ob) mice. Mol Endocrinol. 1994, 8 (4): 518-527.

    CAS  PubMed  Google Scholar 

  32. 32.

    Susulic VS, Frederich RC, Lawitts J, Tozzo E, Kahn BB, Harper ME, Himms-Hagen J, Flier JS, Lowell BB: Targeted disruption of the beta 3-adrenergic receptor gene. J Biol Chem. 1995, 270 (49): 29483-29492.

    CAS  PubMed  Article  Google Scholar 

  33. 33.

    Cannon B, Nedergaard J, Lundberg JM, Hokfelt T, Terenius L, Goldstein M: 'Neuropeptide tyrosine' (NPY) is co-stored with noradrenaline in vascular but not in parenchymal sympathetic nerves of brown adipose tissue. Exp Cell Res. 1986, 164 (2): 546-550.

    CAS  PubMed  Article  Google Scholar 

  34. 34.

    Lever JD, Mukherjee S, Norman D, Symons D, Jung RT: Neuropeptide and noradrenaline distributions in rat interscapular brown fat and in its intact and obstructed nerves of supply. J Auton Nerv Syst. 1988, 25 (1): 15-25.

    CAS  PubMed  Article  Google Scholar 

  35. 35.

    Norman D, Mukherjee S, Symons D, Jung RT, Lever JD: Neuropeptides in interscapular and perirenal brown adipose tissue in the rat: a plurality of innervation. J Neurocytol. 1988, 17 (3): 305-311.

    CAS  PubMed  Article  Google Scholar 

  36. 36.

    Mukherjee S, Lever JD, Norman D, Symons D, Spriggs TL, Jung RT: A comparison of the effects of 6-hydroxydopamine and reserpine on noradrenergic and peptidergic nerves in rat brown adipose tissue. J Anat. 1989, 167: 189-193.

    PubMed Central  CAS  PubMed  Google Scholar 

  37. 37.

    De Matteis R, Ricquier D, Cinti S: TH-, NPY-, SP-, and CGRP-immunoreactive nerves in interscapular brown adipose tissue of adult rats acclimated at different temperatures: an immunohistochemical study. J Neurocytol. 1998, 27 (12): 877-886.

    CAS  PubMed  Article  Google Scholar 

  38. 38.

    Chakraborty TR, Tkalych O, Nanno D, Garcia AL, Devi LA, Salton SR: Quantification of VGF- and pro-SAAS-derived peptides in endocrine tissues and the brain, and their regulation by diet and cold stress. Brain Res. 2006, 1089 (1): 21-32.

    CAS  PubMed  Article  Google Scholar 

  39. 39.

    Cinti S: Adipose tissues and obesity. Ital J Anat Embryol. 1999, 104 (2): 37-51.

    CAS  PubMed  Google Scholar 

  40. 40.

    Cinti S: The role of brown adipose tissue in human obesity. Nutr Metab Cardiovasc Dis. 2006, 16 (8): 569-574.

    PubMed  Article  Google Scholar 

  41. 41.

    Shinozaki K, Shimizu Y, Shiina T, Nishijima K, Atoji Y, Nikami H, Niijima A, Takewaki T: A neurophysiological evidence of capsaicin-sensitive nerve components innervating interscapular brown adipose tissue. Auton Neurosci. 2005, 119 (1): 16-24.

    PubMed  Article  Google Scholar 

  42. 42.

    Bradley RL, Mansfield JP, Maratos-Flier E: Neuropeptides, including neuropeptide Y and melanocortins, mediate lipolysis in murine adipocytes. Obes Res. 2005, 13 (4): 653-661.

    CAS  PubMed  Article  Google Scholar 

  43. 43.

    Kuo LE, Kitlinska JB, Tilan JU, Li L, Baker SB, Johnson MD, Lee EW, Burnett MS, Fricke ST, Kvetnansky R, et al: Neuropeptide Y acts directly in the periphery on fat tissue and mediates stress-induced obesity and metabolic syndrome. Nat Med. 2007, 13 (7): 803-811.

    CAS  PubMed  Article  Google Scholar 

  44. 44.

    Ruohonen ST, Pesonen U, Moritz N, Kaipio K, Roytta M, Koulu M, Savontaus E: Transgenic Mice Overexpressing Neuropeptide Y in Noradrenergic Neurons: A Novel Model of Increased Adiposity and Impaired Glucose Tolerance. Diabetes. 2008, 57 (6): 1517-1525.

    CAS  PubMed  Article  Google Scholar 

  45. 45.

    Kos K, Harte AL, James S, Snead DR, O'Hare JP, McTernan PG, Kumar S: Secretion of neuropeptide Y in human adipose tissue and its role in maintenance of adipose tissue mass. Am J Physiol Endocrinol Metab. 2007, 293 (5): E1335-1340.

    CAS  PubMed  Article  Google Scholar 

  46. 46.

    Yang K, Guan H, Arany E, Hill DJ, Cao X: Neuropeptide Y is produced in visceral adipose tissue and promotes proliferation of adipocyte precursor cells via the Y1 receptor. FASEB J. 2008, 22 (7): 2452-2464.

    CAS  PubMed  Article  Google Scholar 

  47. 47.

    Sudo M, Minokoshi Y, Shimazu T: Ventromedial hypothalamic stimulation enhances peripheral glucose uptake in anesthetized rats. Am J Physiol. 1991, 261 (3 Pt 1): E298-303.

    CAS  PubMed  Google Scholar 

  48. 48.

    Langin D, Lucas S, Lafontan M: Millennium fat-cell lipolysis reveals unsuspected novel tracks. Horm Metab Res. 2000, 32 (11-12): 443-452.

    CAS  PubMed  Article  Google Scholar 

  49. 49.

    Liu CY, Liang LC, Chang LC: Differential responses of hormone-sensitive lipase gene to nutritional transition in adipose tissue, liver, and skeletal muscle of pigs. Biochem Mol Biol Int. 1995, 36 (3): 689-694.

    CAS  PubMed  Google Scholar 

  50. 50.

    Li Y, Bujo H, Takahashi K, Shibasaki M, Zhu Y, Yoshida Y, Otsuka Y, Hashimoto N, Saito Y: Visceral fat: higher responsiveness of fat mass and gene expression to calorie restriction than subcutaneous fat. Exp Biol Med (Maywood). 2003, 228 (10): 1118-1123.

    CAS  Google Scholar 

  51. 51.

    Bertile F, Criscuolo F, Oudart H, Le Maho Y, Raclot T: Differences in the expression of lipolytic-related genes in rat white adipose tissues. Biochem Biophys Res Commun. 2003, 307 (3): 540-546.

    CAS  PubMed  Article  Google Scholar 

  52. 52.

    Jocken JW, Langin D, Smit E, Saris WH, Valle C, Hul GB, Holm C, Arner P, Blaak EE: Adipose triglyceride lipase and hormone-sensitive lipase protein expression is decreased in the obese insulin-resistant state. J Clin Endocrinol Metab. 2007, 92 (6): 2292-2299.

    CAS  PubMed  Article  Google Scholar 

  53. 53.

    Sukonina V, Lookene A, Olivecrona T, Olivecrona G: Angiopoietin-like protein 4 converts lipoprotein lipase to inactive monomers and modulates lipase activity in adipose tissue. Proc Natl Acad Sci USA. 2006, 103 (46): 17450-17455.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  54. 54.

    Kageyama H, Hirano T, Okada K, Ebara T, Kageyama A, Murakami T, Shioda S, Adachi M: Lipoprotein lipase mRNA in white adipose tissue but not in skeletal muscle is increased by pioglitazone through PPAR-gamma. Biochem Biophys Res Commun. 2003, 305 (1): 22-27.

    CAS  PubMed  Article  Google Scholar 

  55. 55.

    Laplante M, Sell H, MacNaul KL, Richard D, Berger JP, Deshaies Y: PPAR-gamma activation mediates adipose depot-specific effects on gene expression and lipoprotein lipase activity: mechanisms for modulation of postprandial lipemia and differential adipose accretion. Diabetes. 2003, 52 (2): 291-299.

    CAS  PubMed  Article  Google Scholar 

  56. 56.

    Schoonjans K, Peinado-Onsurbe J, Lefebvre AM, Heyman RA, Briggs M, Deeb S, Staels B, Auwerx J: PPARalpha and PPARgamma activators direct a distinct tissue-specific transcriptional response via a PPRE in the lipoprotein lipase gene. Embo J. 1996, 15 (19): 5336-5348.

    PubMed Central  CAS  PubMed  Google Scholar 

  57. 57.

    Kuusela P, Jacobsson A, Klingenspor M, Rehnmark S, Heldmaier G, Cannon B, Nedergaard J: Contrasting adrenergic effects on lipoprotein lipase gene expression in the brown adipose tissue of intact mice and in cultured brown adipocytes from mice. Biochim Biophys Acta. 1997, 1345 (3): 327-337.

    CAS  PubMed  Article  Google Scholar 

  58. 58.

    Uldry M, Yang W, St-Pierre J, Lin J, Seale P, Spiegelman BM: Complementary action of the PGC-1 coactivators in mitochondrial biogenesis and brown fat differentiation. Cell Metab. 2006, 3 (5): 333-341.

    CAS  PubMed  Article  Google Scholar 

  59. 59.

    Griggio MA: The participation of shivering and nonshivering thermogenesis in warm and cold-acclimated rats. Comp Biochem Physiol A. 1982, 73 (3): 481-484.

    CAS  PubMed  Article  Google Scholar 

  60. 60.

    Sell H, Berger JP, Samson P, Castriota G, Lalonde J, Deshaies Y, Richard D: Peroxisome proliferator-activated receptor gamma agonism increases the capacity for sympathetically mediated thermogenesis in lean and ob/ob mice. Endocrinology. 2004, 145 (8): 3925-3934.

    CAS  PubMed  Article  Google Scholar 

  61. 61.

    Hamilton JM, Mason PW, McElroy JF, Wade GN: Dissociation of sympathetic and thermogenic activity in brown fat of Syrian hamsters. Am J Physiol. 1986, 250 (3 Pt 2): R389-395.

    CAS  PubMed  Google Scholar 

  62. 62.

    McElroy JF, Wade GN: Short photoperiod stimulates brown adipose tissue growth and thermogenesis but not norepinephrine turnover in Syrian hamsters. Physiol Behav. 1986, 37 (2): 307-311.

    CAS  PubMed  Article  Google Scholar 

  63. 63.

    Sigurdson SL, Himms-Hagen J: Control of norepinephrine turnover in brown adipose tissue of Syrian hamsters. Am J Physiol. 1988, 254 (6 Pt 2): R960-968.

    CAS  PubMed  Google Scholar 

  64. 64.

    Giordano A, Frontini A, Murano I, Tonello C, Marino MA, Carruba MO, Nisoli E, Cinti S: Regional-dependent increase of sympathetic innervation in rat white adipose tissue during prolonged fasting. J Histochem Cytochem. 2005, 53 (6): 679-687.

    CAS  PubMed  Article  Google Scholar 

  65. 65.

    Penn DM, Jordan LC, Kelso EW, Davenport JE, Harris RB: Effects of central or peripheral leptin administration on norepinephrine turnover in defined fat depots. Am J Physiol Regul Integr Comp Physiol. 2006, 291 (6): R1613-1621.

    CAS  PubMed  Article  Google Scholar 

  66. 66.

    Watson E: VGF: A regulator of energy and glucose homeostasis. Understanding VGF's mechanism of action in modulating autonomic homeostasis. PhD Dissertation. 2006, Mount Sinai School of Medicine of New York University

    Google Scholar 

  67. 67.

    Gautam D, Gavrilova O, Jeon J, Pack S, Jou W, Cui Y, Li JH, Wess J: Beneficial metabolic effects of M3 muscarinic acetylcholine receptor deficiency. Cell Metab. 2006, 4 (5): 363-375.

    CAS  PubMed  Article  Google Scholar 

  68. 68.

    van Baak MA: The peripheral sympathetic nervous system in human obesity. Obes Rev. 2001, 2 (1): 3-14.

    CAS  PubMed  Article  Google Scholar 

  69. 69.

    Landsberg L: Feast or famine: the sympathetic nervous system response to nutrient intake. Cell Mol Neurobiol. 2006, 26 (4-6): 497-508.

    CAS  PubMed  Article  Google Scholar 

  70. 70.

    Tentolouris N, Liatis S, Katsilambros N: Sympathetic system activity in obesity and metabolic syndrome. Ann N Y Acad Sci. 2006, 1083: 129-152.

    CAS  PubMed  Article  Google Scholar 

  71. 71.

    Ahima RS: Adipose tissue as an endocrine organ. Obesity (Silver Spring). 2006, 14 (Suppl 5): 242S-249S.

    CAS  Article  Google Scholar 

  72. 72.

    Campfield LA, Smith FJ, Guisez Y, Devos R, Burn P: Recombinant mouse OB protein: evidence for a peripheral signal linking adiposity and central neural networks. Science. 1995, 269 (5223): 546-549.

    CAS  PubMed  Article  Google Scholar 

  73. 73.

    Halaas JL, Gajiwala KS, Maffei M, Cohen SL, Chait BT, Rabinowitz D, Lallone RL, Burley SK, Friedman JM: Weight-reducing effects of the plasma protein encoded by the obese gene. Science. 1995, 269 (5223): 543-546.

    CAS  PubMed  Article  Google Scholar 

  74. 74.

    Pelleymounter MA, Cullen MJ, Baker MB, Hecht R, Winters D, Boone T, Collins F: Effects of the obese gene product on body weight regulation in ob/ob mice. Science. 1995, 269 (5223): 540-543.

    CAS  PubMed  Article  Google Scholar 

  75. 75.

    Dobbins RL, Szczepaniak LS, Zhang W, McGarry JD: Chemical sympathectomy alters regulation of body weight during prolonged ICV leptin infusion. Am J Physiol Endocrinol Metab. 2003, 284 (4): E778-787.

    CAS  PubMed  Article  Google Scholar 

  76. 76.

    Balthasar N, Dalgaard LT, Lee CE, Yu J, Funahashi H, Williams T, Ferreira M, Tang V, McGovern RA, Kenny CD, et al: Divergence of melanocortin pathways in the control of food intake and energy expenditure. Cell. 2005, 123 (3): 493-505.

    CAS  PubMed  Article  Google Scholar 

  77. 77.

    Butler AA, Marks DL, Fan W, Kuhn CM, Bartolome M, Cone RD: Melanocortin-4 receptor is required for acute homeostatic responses to increased dietary fat. Nat Neurosci. 2001, 4 (6): 605-611.

    CAS  PubMed  Article  Google Scholar 

  78. 78.

    Schaak S, Mialet-Perez J, Flordellis C, Paris H: Genetic variation of human adrenergic receptors: from molecular and functional properties to clinical and pharmacogenetic implications. Curr Top Med Chem. 2007, 7 (2): 217-231.

    CAS  PubMed  Article  Google Scholar 

  79. 79.

    Bachman ES, Dhillon H, Zhang CY, Cinti S, Bianco AC, Kobilka BK, Lowell BB: betaAR signaling required for diet-induced thermogenesis and obesity resistance. Science. 2002, 297 (5582): 843-845.

    CAS  PubMed  Article  Google Scholar 

  80. 80.

    Jimenez M, Leger B, Canola K, Lehr L, Arboit P, Seydoux J, Russell AP, Giacobino JP, Muzzin P, Preitner F: Beta(1)/beta(2)/beta(3)-adrenoceptor knockout mice are obese and cold-sensitive but have normal lipolytic responses to fasting. FEBS Lett. 2002, 530 (1-3): 37-40.

    CAS  PubMed  Article  Google Scholar 

  81. 81.

    Demas GE, Bartness TJ: Direct innervation of white fat and adrenal medullary catecholamines mediate photoperiodic changes in body fat. Am J Physiol Regul Integr Comp Physiol. 2001, 281 (5): R1499-1505.

    CAS  PubMed  Google Scholar 

  82. 82.

    Demas GE, Bowers RR, Bartness TJ, Gettys TW: Photoperiodic regulation of gene expression in brown and white adipose tissue of Siberian hamsters (Phodopus sungorus). Am J Physiol Regul Integr Comp Physiol. 2002, 282 (1): R114-121.

    CAS  PubMed  Google Scholar 

  83. 83.

    Tavernier G, Jimenez M, Giacobino JP, Hulo N, Lafontan M, Muzzin P, Langin D: Norepinephrine induces lipolysis in beta1/beta2/beta3-adrenoceptor knockout mice. Mol Pharmacol. 2005, 68 (3): 793-799.

    CAS  PubMed  Google Scholar 

  84. 84.

    Ste Marie L, Luquet S, Curtis W, Palmiter RD: Norepinephrine- and epinephrine-deficient mice gain weight normally on a high-fat diet. Obes Res. 2005, 13 (9): 1518-1522.

    CAS  PubMed  Article  Google Scholar 

  85. 85.

    Salton SR, Fischberg DJ, Dong KW: Structure of the gene encoding VGF, a nervous system-specific mRNA that is rapidly and selectively induced by nerve growth factor in PC12 cells. Mol Cell Biol. 1991, 11 (5): 2335-2349.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  86. 86.

    Snyder SE, Pintar JE, Salton SR: Developmental expression of VGF mRNA in the prenatal and postnatal rat. J Comp Neurol. 1998, 394 (1): 64-90.

    CAS  PubMed  Article  Google Scholar 

  87. 87.

    Chan MY, Zhao Y, Heng CK: Sequential responses to high-fat and high-calorie feeding in an obese mouse model. Obesity (Silver Spring). 2008, 16 (5): 972-978.

    CAS  Article  Google Scholar 

  88. 88.

    Lin S, Thomas TC, Storlien LH, Huang XF: Development of high fat diet-induced obesity and leptin resistance in C57Bl/6J mice. Int J Obes Relat Metab Disord. 2000, 24 (5): 639-646.

    CAS  PubMed  Article  Google Scholar 

  89. 89.

    Mastaitis J: Regulation of hypothalamic gene expression during hypoglycemia and low-carbohydrate diets. Ph.D. Dissertation, Graduate School of Biological Sciences, Mount Sinai School of Medicine. 2007, 1-136.

    Google Scholar 

  90. 90.

    Bartolomucci A, La Corte G, Possenti R, Locatelli V, Rigamonti AE, Torsello A, Bresciani E, Bulgarelli I, Rizzi R, Pavone F, et al: TLQP-21, a VGF-derived peptide, increases energy expenditure and prevents the early phase of diet-induced obesity. Proc Natl Acad Sci USA. 2006, 103 (39): 14584-14589.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  91. 91.

    Jethwa P, Warner A, Nilaweera K, Brameld J, Keyte J, Carter W, Bolton N, Bruggraber M, Morgan P, Barrett P, et al: VGF-derived peptide, TLQP-21, regulates food intake and body weight in Siberian hamsters. Endocrinology. 2007, 148 (8): 4044-4055.

    CAS  PubMed  Article  Google Scholar 

  92. 92.

    Trani E, Ciotti T, Rinaldi AM, Canu N, Ferri GL, Levi A, Possenti R: Tissue-specific processing of the neuroendocrine protein VGF. J Neurochem. 1995, 65 (6): 2441-2449.

    CAS  PubMed  Article  Google Scholar 

  93. 93.

    Trani E, Giorgi A, Canu N, Amadoro G, Rinaldi AM, Halban PA, Ferri GL, Possenti R, Schinina ME, Levi A: Isolation and characterization of VGF peptides in rat brain. Role of PC1/3 and PC2 in the maturation of VGF precursor. J Neurochem. 2002, 81 (3): 565-574.

    CAS  PubMed  Article  Google Scholar 

  94. 94.

    Bartolomucci A, Possenti R, Levi A, Pavone F, Moles A: The role of the vgf gene and VGF-derived peptides in nutrition and metabolism. Genes Nutr. 2007, 2: 169-180.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  95. 95.

    Bozdagi O, Rich E, Tronel S, Sadahiro M, Patterson K, Shapiro ML, Alberini CM, Huntley GW, Salton SR: The neurotrophin-inducible gene Vgf regulates hippocampal function and behavior through a brain-derived neurotrophic factor-dependent mechanism. J Neurosci. 2008, 28 (39): 9857-9869.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  96. 96.

    Severini C, Ciotti MT, Biondini L, Quaresima S, Rinaldi AM, Levi A, Frank C, Possenti R: TLQP-21, a neuroendocrine VGF-derived peptide, prevents cerebellar granule cells death induced by serum and potassium deprivation. J Neurochem. 2008, 104 (2): 534-544.

    CAS  PubMed  Google Scholar 

  97. 97.

    Severini C, La Corte G, Improta G, Broccardo M, Agostini S, Petrella C, Sibilia V, Pagani F, Guidobono F, Bulgarelli I, et al: In vitro and in vivo pharmacological role of TLQP-21, a VGF-derived peptide, in the regulation of rat gastric motor functions. Br J Pharmacol. 2009, 157 (6): 984-993.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  98. 98.

    Salton SR, Volonte C, D'Arcangelo G: Stimulation of vgf gene expression by NGF is mediated through multiple signal transduction pathways involving protein phosphorylation. FEBS Lett. 1995, 360 (2): 106-110.

    CAS  PubMed  Article  Google Scholar 

  99. 99.

    Fields-Berry SC, Halliday AL, Cepko CL: A recombinant retrovirus encoding alkaline phosphatase confirms clonal boundary assignment in lineage analysis of murine retina. Proc Natl Acad Sci USA. 1992, 89 (2): 693-697.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  100. 100.

    Fire A: Histochemical techniques for locating Escherichia coli beta-galactosidase activity in transgenic organisms. Genet Anal Tech Appl. 1992, 9 (5-6): 151-158.

    CAS  PubMed  Article  Google Scholar 

  101. 101.

    Mzhavia N, Berman Y, Che FY, Fricker LD, Devi LA: ProSAAS processing in mouse brain and pituitary. J Biol Chem. 2001, 276 (9): 6207-6213.

    CAS  PubMed  Article  Google Scholar 

  102. 102.

    Sleeman MW, Garcia K, Liu R, Murray JD, Malinova L, Moncrieffe M, Yancopoulos GD, Wiegand SJ: Ciliary neurotrophic factor improves diabetic parameters and hepatic steatosis and increases basal metabolic rate in db/db mice. Proc Natl Acad Sci USA. 2003, 100 (24): 14297-14302.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  103. 103.

    Wortley KE, Garcia K, Okamoto H, Thabet K, Anderson KD, Shen V, Herman JP, Valenzuela D, Yancopoulos GD, Tschop MH, et al: Peptide YY regulates bone turnover in rodents. Gastroenterology. 2007, 133 (5): 1534-1543.

    CAS  PubMed  Article  Google Scholar 

  104. 104.

    Johnson EM, Cantor E, Douglas JR: Biochemical and functional evaluation of the sympathectomy produced by the administration of guanethidine to newborn rats. J Pharmacol Exp Ther. 1975, 193 (2): 503-512.

    PubMed  Google Scholar 

  105. 105.

    Demas GE, Bartness TJ: Novel method for localized, functional sympathetic nervous system denervation of peripheral tissue using guanethidine. J Neurosci Methods. 2001, 112 (1): 21-28.

    CAS  PubMed  Article  Google Scholar 

Download references


Supported in part by NIH Endocrine Training Grant 5T32DK07645 (EW and SF), RO1 DK071308 (SRS), RO1 DK57702 (SRS), the American Heart Association (SRS), and the Diabetes Action Research and Education Foundation (SRS). SRS is a NARSAD van Ameringen Investigator. We thank Carla Montgomery and Heather Bell for technical assistance, and Dr. Susan Morgello and Noreen Mall in the Mount Sinai Shared Research Facility Histology Service for assistance with the adipose tissue analysis.

Author information



Corresponding author

Correspondence to Stephen R Salton.

Additional information

Authors' contributions

EW carried out histological analysis, metabolic studies, real-time PCR experiments, and drafted the manuscript, SF carried out histological and EM analysis, morphometry, western blot analysis, and helped to draft the manuscript; HO carried out the metabolic and feeding analysis, whole mount β-galactosidase staining, and serum analysis; MS carried out the breeding and genotyping of VGF-deficient mice and assisted with histological, EM and western analysis; REG assisted with the design and coordination of the electron microscopic analysis; TC carried out the RIA analysis; MWS participated in the design and coordination of the study; SRS participated in the design and coordination of the study, and drafted the manuscript. All authors read and approved the final manuscript.

Elizabeth Watson, Samira Fargali contributed equally to this work.

Electronic supplementary material

Supplemental Figure 1. Lipid deposition in multilocular cells of brown adipose tissue (BAT) and unilocular cells of white adipose tissue (WAT) is reduced in VGF

Additional file 1: C57 knockout mice. Representative sections of interscapular BAT (A-D) and epididymal WAT (E-F) from ad lib-fed VgfC 57-/- (A, C and E) and age-matched VgfC 57+/+ (B, D, and F) mice were stained with H&E. The interscapular WAT that normally surrounds BAT in wild type mice (D) was absent in VGF-deficient mice (A and C). Adipocytes in interscapular BAT and epididymal WAT from VgfC 57-/- mice (A and E) contain less lipid accumulation than the corresponding adipocytes from wild type mice (B and F). Scale bars are 100 μm in length. (PDF 154 KB)

Supplemental Figure 2. Neonatal chemical sympathectomy with guanethidine (GE) increases fat and glycogen stores and plasma glucose levels in GE-treated VGF knockout mice

Additional file 2: . H&E staining of liver, BAT, and epididymal WAT from 4 month-old VgfC 57-/- mice treated daily with GE (50 mg/kg) or saline (control) from postnatal day 5 (P5) until P25, essentially as previously described [104, 105], which results in permanent sympathectomy. At 4 months of age, mice were anesthetized, blood samples collected, and glucose levels determined by glucometer; tissues were removed and formalin-fixed for histological analysis. Note that clear areas in liver, corresponding to glycogen deposits, are increased in GE-treated VgfC 57-/- mice compared to saline-treated control VgfC 57-/- mice (panels A and B). BAT in GE-treated VgfC 57-/- mice is bordered by WAT (arrows), which is reduced in saline-treated VgfC 57-/- mice (panels C and D). Fat storage is reduced in WAT from saline-treated compared to GE-treated VgfC 57-/- mice (panels E and F). Scale bars are 100 μm in length. GE-treatment significantly increased circulating glucose levels in VgfC 57-/- but not in VgfC 57+/- mice compared to their respective saline-treated controls (panel G; ANOVA, p < 0.05, mean ± SEM). (PDF 226 KB)

Supplemental Figure 3. Immunohistochemical localization of VGF protein in BAT

Additional file 3: . Immunohistochemical staining of BAT with anti-VGF and anti-tyrosine hydroxylase (TH) antisera in wild-type mice was carried out, and showed similar patterns. Sections were stained with rabbit anti-VGF78-340 [98] (panels A, C, and D) and anti-TH (Chemicon International, Temecula, CA) (panel B) (in panels A and B, arrows point to VGF positive and TH positive fibers, respectively). Note that VGF immunoreactivity is also seen in the adventitia of small arterioles (panel C; arrows). In addition, VGF-positive puncta in direct contact with the brown adipocyte (panel D) were visualized using immunofluorescent staining. Scale bars are 100 μm (panels A-C) and 10 μm (panel D). (PDF 115 KB)

Authors’ original submitted files for images

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Watson, E., Fargali, S., Okamoto, H. et al. Analysis of knockout mice suggests a role for VGF in the control of fat storage and energy expenditure. BMC Physiol 9, 19 (2009).

Download citation


  • Brown Adipose Tissue
  • Hormone Sensitive Lipase
  • Interscapular Brown Adipose Tissue
  • UCP1 Gene Expression
  • C57Bl6 Background