- Research article
- Open Access
Identification of uterine ion transporters for mineralisation precursors of the avian eggshell
© Jonchère et al.; licensee BioMed Central Ltd. 2012
Received: 24 April 2012
Accepted: 16 August 2012
Published: 4 September 2012
In Gallus gallus, eggshell formation takes place daily in the hen uterus and requires large amounts of the ionic precursors for calcium carbonate (CaCO3). Both elements (Ca2+, HCO3-) are supplied by the blood via trans-epithelial transport. Our aims were to identify genes coding for ion transporters that are upregulated in the uterine portion of the oviduct during eggshell calcification, compared to other tissues and other physiological states, and incorporate these proteins into a general model for mineral transfer across the tubular gland cells during eggshell formation.
A total of 37 candidate ion transport genes were selected from our database of overexpressed uterine genes associated with eggshell calcification, and by analogy with mammalian transporters. Their uterine expression was compared by qRTPCR in the presence and absence of eggshell formation, and with relative expression levels in magnum (low Ca2+/HCO3- movement) and duodenum (high rates of Ca2+/HCO3- trans-epithelial transfer). We identified overexpression of eleven genes related to calcium movement: the TRPV6 Ca2+ channel (basolateral uptake of Ca2+), 28 kDa calbindin (intracellular Ca2+ buffering), the endoplasmic reticulum type 2 and 3 Ca2+ pumps (ER uptake), and the inositol trisphosphate receptors type 1, 2 and 3 (ER release). Ca2+ movement across the apical membrane likely involves membrane Ca2+ pumps and Ca2+/Na+ exchangers. Our data suggests that Na+ transport involved the SCNN1 channel and the Na+/Ca2+ exchangers SLC8A1, 3 for cell uptake, the Na+/K+ ATPase for cell output. K+ uptake resulted from the Na+/K+ ATPase, and its output from the K+ channels (KCNJ2, 15, 16 and KCNMA1).
We propose that the HCO3- is mainly produced from CO2 by the carbonic anhydrase 2 (CA2) and that HCO3- is secreted through the HCO3-/Cl- exchanger SLC26A9. HCO3- synthesis and precipitation with Ca2+ produce two H+. Protons are absorbed via the membrane’s Ca2+ pumps ATP2B1, 2 in the apical membrane and the vacuolar (H+)-atpases at the basolateral level. Our model incorporate Cl- ions which are absorbed by the HCO3-/Cl- exchanger SLC26A9 and by Cl- channels (CLCN2, CFTR) and might be extruded by Cl-/H+ exchanger (CLCN5), but also by Na+ K+ 2 Cl- and K+ Cl- cotransporters.
Our Gallus gallus uterine model proposes a large list of ion transfer proteins supplying Ca2+ and HCO3- and maintaining cellular ionic homeostasis. This avian model should contribute towards understanding the mechanisms and regulation for ionic precursors of CaCO3, and provide insight in other species where epithelia transport large amount of calcium or bicarbonate.
PH and ion concentrations in blood plasma, uterine fluid and epithelial cells during eggshell mineralisation
8 h PO
18 h PO
The second essential component of eggshell mineralisation is carbonate. Blood carbon dioxide (CO2) is provided in cells by passive diffusion through the plasma membrane [2, 19]. In the uterine tubular gland cells, a family of key enzymes, the carbonic anhydrases (CA)  catalyses the hydration of CO2 to HCO3- as confirmed by inhibition of HCO3- production and secretion by acetazolamide, a CA inhibitor . Chloride (Cl-) is absorbed by the uterus and any perturbation of Na+ flux by ouabain  reverses both the Na+ and Cl- fluxes, but reduces also HCO3- secretion suggesting that its transfer is dependent on Cl- via a Cl-/HCO3- exchanger which has not been identified. Finally, the production of HCO3- in tubular gland cells and of CO32- in the uterine fluid generates high levels of protons (H+) ions. The concomitant decrease in uterine and plasma pH during calcification reflects the reabsorption of H+.
Only a few genes and related proteins involved in uterine ion transfer have been identified to date. Our objective therefore was to use the recent information issuing from the chicken genome sequencing  and subsequent enrichment in the chicken gene/protein databases to identify uterine ion transport proteins. Use of a recent transcriptomic study revealing uterine genes related to eggshell calcification  and of the analogies with transporters previously described in mammalian tissues transferring large quantities of ions (intestine, kidney, pancreas) allows the identification of putative genes encoding proteins involved in uterine trans-epithelial ion transports. Confirmation of their presence in birds and evaluation of their involvement have been analysed by comparing gene expression in the uterus compared to the magnum (the oviduct segment responsible for the synthesis and secretion of egg white proteins) and the duodenum (Ca2+ uptake and neutralization of stomach acid), where both Ca2+ and HCO3- trans-epithelial transfers are respectively low and high. The magnum and the uterus secrete a large amount of water, Na + and Cl- during the phase of hydration of egg albumen which takes place before the active phase of eggshell formation in the uterus [5, 22]. By contrast, the duodenum is the proximal region of the intestine with a high capacity for Ca2+ absorption  and secretes a large amount of HCO3- for neutralization of gastric acidity [24, 25]. An additional experimental approach was the comparison of gene expression in the uterus isolated from hens at the stage of eggshell formation, to those for which eggshell formation was suppressed by premature egg expulsion. We identified a large number of genes coding for ion transport and propose a general model describing the putative contribution and localisation of the ion transporters in the tubular gland cell of the hen’s uterus.
Identification of uterine ion transporters
Function of genes potentially involved in the ion transfer for supplying eggshell mineral precursors in hen uterus
Transient receptor potential cation channel subfamily V member 6
Ca2+ channel (plasma membrane)
Calbindin 28 K
Ca2+ intracellular transporter (intracellular)
Endoplasmic reticulum calcium ATPase 1
Ca2+ ATPases (endoplasmic & plasma membrane)
Endoplasmic reticulum calcium ATPase 2
Endoplasmic reticulum calcium ATPase 3)
Ca2+ channels (endoplasmic membrane)
Ryanodine receptor 1
Ca2+ channel (endoplasmic membrane)
Plasma membrane calcium-transporting ATPase 1 (PMCA1)
Ca2+/H+ exchanger (plasma membrane)
Plasma membrane calcium-transporting ATPase 2 (PMCA2)
Plasma membrane calcium-transporting ATPase 4 (PMCA4)
Sodium/calcium exchanger 1
Na+/Ca2+ exchanger (plasma membrane)
Sodium/calcium exchanger 3
Amiloride-sensitive sodium channel subunit alpha
Na+ channels (plasma membrane)
Amiloride-sensitive sodium channel subunit beta
Amiloride-sensitive sodium channel subunit gamma
Sodium/potassium-transporting ATPase subunit alpha-1
Na+/K+ exchanger (plasma membrane)
Sodium/potassium-transporting ATPase subunit beta-1
Solute carrier family 4 member 4
Na+/HCO3- co-transporters (plasma membrane)
Solute carrier family 4 member 5
Solute carrier family 4 member 7
Solute carrier family 4 member 10
Inward rectifier potassium channel 2
Inward rectifiers K+ channels (plasma membrane)
Inward rectifier potassium channel 5
Inward rectifier potassium channel 16
Calcium-activated potassium channel subunit alpha-1
K+ channel (plasma membrane)
Carbonic anhydrase 2
Catalyse HCO3- formation (plasma membrane)
Carbonic anhydrase 4
Carbonic anhydrase 7
Solute carrier family 4 member 8
HCO3-/Cl- exchangers (plasma membrane)
Solute carrier family 4 member 9
Solute carrier family 26 member 9
Vacuolar H ATPase B subunit osteoclast isozyme
H+ pump (organelles and plasma membrane
Cystic fibrosis transmembrane conductance regulator
Cl- channel (plasma membrane)
Chloride channel protein 2
Cl- channel (plasma membrane)
H(+)/Cl(−) exchange transporter 5
Cl-/H+ exchanger (plasma membrane)
Uterine expression of the 37 genes encoding ion transporters
The mRNA expression of 37 transporters was analysed by RT-PCR in the uterus, and three other ion secreting or absorbing epithelia (magnum, duodenum and kidney) and in muscle where no trans-epithelial ion transfer occurs (Additional file 1: Table 1). Amongst these 37 genes, mRNA expression was observed in the uterus for 34 genes. Three genes (the endoplasmic Ca2+ pump type 1(ATP2A1), two exchangers Na+ dependent (SLC4A8) or independent (SLC4A9) Cl-/HCO3- were not expressed in the uterus and were not further studied.
A large majority of these 34 genes were also revealed in the duodenum. Conversely, SLC4A8 was expressed only in duodenum. Four genes were revealed only in the uterus and were not present in the magnum (TRPV6, CALB1, SCNN1B and SLC26A9) or in muscle (CALB1, SCNN1B, SLC4A10 and CLCN2). The 34 genes revealed in the uterus are candidates for supplying ions in the uterus.
Comparative expression of ion transfer genes between uterus and other secreting tissues
Ca2+ transfer: TRPV Ca2± channel (TRPV6), calbindin 28 kDa (CALB1), endoplasmic Ca2± pump type 2 and 3 (ATP2A2, 3), inositol trisphosphate receptor type 1, 2, 3 (ITPR1, 2, 3), Ca2± pumps PMCA type 1, 2 and 4 (ATP2B1, 2, 4) and Ca2±/Na± exchanger type 1, 3 (SLC8A1, 3).
Na+ transfer: amiloride-sensitive Na + channel subunit α, β, and γ (SCNN1A, B, G), Na±/K ± transporting ATPase subunit α and β (ATP1A1, B1), Ca2±/Na± exchanger type 1 and 3 (SLC8A1, 3), several Na±/HCO3 - co-transporters (SLC4A4, 5, 7, 10).
K+ transfer: Na±/K ± transporting ATPase subunit α and β (ATP1A1, B1) and several K± channels (KCNJ2, 15, 16, KCNMA1).
HCO3 - production and transfer: CAs type 2, 4, 7, (CA2, 4, 7), an HCO3 -/Cl- exchanger (SLC26A9), and several Na±/HCO3 - co-transporters (SLC4A4, 5, 7, 10).
H+ transfer: VH± ATPase pump subunit B (ATP6V1B2), and Cl-/H+ exchanger (CLCN5).
Cl- transfer: CFTR channel (CFTR), Cl- channel protein 2 (CLCN2), an HCO3 -/Cl- exchanger (SLC26A9) and a Cl-/H+ exchanger (CLCN5).
Ca2+ transfer: endoplasmic Ca2+ pump type 3 (ATP2A3), inositol trisphosphate receptors (ITPR1, 2), Ca2+ pumps PMCA2 (ATP2B2) and Ca2+/Na+ exchanger type 3 (SLC8A3).
Na+ transfer: amiloride-sensitive Na + channel subunit α, β, and γ (SCNN1A, B, G), Ca2+/Na+ exchanger type 3 (SLC8A3), Na+/HCO3 - co-transporters (SLC4A5).
K+ transfer: several K+ channels (KCNJ2, 16 and KCNMA1).
HCO3 - production and transfer: Na+/HCO3 - co-transporters (SLC4A5).
Cl- transfer: Cl- channel protein 2 (CLCN2) and CFTR channel (CFTR).
Ca2+ transfer: Ca2+ pumps PMCA1 (ATP2B1).
HCO3 - production and transfer: CA type 7 (CA7).
H+ transfer and (4) Cl- transfer: H+/Cl- exchanger (CLCN5).
Comparative expression of genes in the presence or absence of eggshell formation
Ca+2+ transfer: 28 kDa calbindin (CALB1), endoplasmic Ca2+ pump type 3 (ATP2A3), and Ca2+ pumps PMCA2 (ATP2B1, 2).
Na+ transfer: amiloride-sensitive Na + channel subunit γ (SCNN1G) and Na+/K+ transporting ATPase subunit α (ATP1A1).
K+ transfer: Na+/K + transporting ATPase subunit α (ATP1A1) and the K+ channels (KCNJ2, KCNJ15 and KCNMA1).
HCO3 - production and transfer: carbonic anhydrase CA type 2 (CA2), an HCO3 -/Cl- exchanger (SLC26A9).
Cl- transfer: the Cl- channel (CFTR) and an HCO3 -/Cl- exchanger (SLC26A9).
In contrast, 2 genes corresponding to a Ca2+/H+ exchanger (ATP2B4) and to a Na+/HCO3- co-transporter (SLC4A7) showed an underexpression when eggshell calcification takes place.
Ca2+ transfer: TRPV Ca2+ channel (TRPV6), endoplasmic Ca2+ pump type 2 (ATP2A2), inositol trisphosphate receptors (ITPR1, 2, 3), and Ca2+/Na+ exchanger type 1 and 3 (SLC8A1, 3).
Na+ transfer: amiloride-sensitive Na + channel subunit α and γ (SCNN1A, B), Na+/K + transporting ATPase subunit β (ATP1B1), Ca2+/Na+ exchanger type 1 and 3 (SLC8A1, 3), Na+/HCO3 - co-transporters (SLC4A4, 5, 10).
K+ transfer: Na+/K + transporting ATPase subunit β (ATP1B1) and a K+ channel (KCNJ16).
HCO3 - production and transfer: CA type 4, 7 (CA4, 7), several Na+/HCO3 - co-transporters (SLC4A4, 5, 10).
Cl- transfer: Cl- channel protein 2 (CLCN2) and H+/Cl- exchanger (CLCN5).
H+ transfer: VH+ ATPase pump subunit B (ATP6V1B2) and H+/Cl- exchanger (CLCN5).
Eggshell calcification in the avian uterus is one of the fastest mineralisation processes in the living world. The Ca2+ metabolism is intense in Gallus gallus hens which export a large amount of Ca2+ (2 g daily) and consequently there are numerous physiological adaptations to support this function [1, 27–30]. In fact, an egg-producing hen shows a specific appetite for Ca2+ a few hours before shell calcification is initiated and its capacity to absorb Ca2+ in the intestine increases by 6-fold due to large stimulation of the active metabolite of vitamin D at the kidney level. The uterus acquires the capacity to transfer a great quantity of Ca2+ and HCO3- for supplying mineral precursors of the eggshell during less than 14 hours. This model is therefore particularly relevant to explore the mechanisms of mineral transport needed for the extracellular biomineralisation of the eggshell. In this study, we focused on intracellular ionic transporters and did not explore the proteins involved in their regulation. This process has been the object of many physiological and pharmacological works as reviewed by Nys  and Bar . However, the molecular identification of ionic transporters remains incomplete in the uterus. Genome sequencing in human and other mammalian species has contributed to the molecular identification of genes and related proteins involved in ionic trans-epithelial transfer in the intestine and kidneys [24, 26]. By using this literature and data provided by a recent high throughput analysis of chicken uterine genes related to eggshell calcification , we identified 37 putative genes encoding ion trans-epithelial transporters and tested their involvement in providing mineral precursors in the hen’s uterus. Analysis of their expression by RT-PCR, showed that 34 of these genes were expressed at the uterine level. In order to study their involvement in providing both Ca2+ and HCO3- for eggshell formation, the expression of these 34 genes in the uterus was quantified by qRT-PCR and compared with two other epithelia (magnum and duodenum) where Ca2+ and HCO3- transfers are respectively low and high. In addition, the expression of these genes was compared in the uterus during two situations: during eggshell calcification and when Ca2+ and HCO3- secretions were suppressed due to premature egg expulsion. These approaches allowed the identification of numerous transporting proteins providing minerals for shell formation in the hen’s uterus.
Ca2+ is not stored in the uterus before eggshell calcification but comes from blood plasma by trans-epithelial transport. This Ca2+ export is extremely rapid during calcification and corresponds to a consumption of the total plasmatic Ca2+ pool every 12 min. Studies of Ca2+ transfer in vivo using perfusion of uterus [8, 9] and in vitro exploring the effects of inhibitors of ion ATPases or carbonic anhydrase [10, 31], and ionic analysis of uterine fluid during eggshell formation , made it possible to build a first model of Ca2+ transfer in the uterus (Figure1): Ca2+, HCO3- secretion and Na+ reabsorption was considered to occur against their electrochemical gradient, to involve active intracellular transfer as shown by specific inhibitors [8–10] and to occur in the uterine glandular cells as revealed by immunohistochemistry of transport proteins . Trans-epithelial transfer of Ca2+ occurs in three steps as observed in all transporting epithelia: Ca2+ influx through a downhill gradient, an intracellular Ca2+ transport involving calbindin 28 kDa protein  and active output into the lumen through a Ca2+ pump . The high plasma Ca2+ concentration (1.2 mM free Ca2+) relative to the uterine cell interior (10-4 mM free Ca2+) (Table1) suggests that the Ca2+ entry into cells passively occurs via Ca2+ selective channels present in the basolateral plasma membrane. In other tissues, such as intestine, kidney and plasma, TRPVs 5, 6 (Transient Receptor Potential Vanilloid) are epithelial channels that represent the principal pathway for Ca2+ uptake into the cell [26, 34]. Our study showed that in Gallus gallus, only one gene [NCBI Gene ID: 418307; Swiss-Prot: TRPV6] is present. This channel is significantly overexpressed in the uterus compared with the magnum, where Ca2+ transfer is low. Its uterine expression is similar to that of the duodenum where Ca2+ absorption is also large. Cellular Ca2+ influx might use a similar Ca2+ channel, TRPV6, at the intestinal and uterine level but their localisation is hypothesized to differ according to the site of Ca2+ influx, being located in the basal membrane in the uterus but in the apical membrane in the intestine. The uterine expression of TRPV6 is not however modified according to whether calcification takes place. The presence of other Ca2+ channels cannot be ruled out as additional putative candidates. A recent transcriptomic study in our laboratory comparing uterine gene expression in hens with or without shell calcification revealed the presence of high expression of TRPC1, TRPP, TRPM7, TRPML1 and ORAI 1 (unpublished data, Brionne A, Nys Y and Gautron J).
An intracellular Ca2+ buffer is crucial to keep the free cytosolic Ca2+ concentration below toxic levels. Following Ca2+ entry into the uterine glandular cell, several systems could contribute to intracellular transport of Ca2+, while maintaining the low but essential free Ca2+ concentration for survival of the cell. In certain tissues, calbindin proteins, 9 kDa and 28 kDa in mammals  or 28 kDa in birds [3, 35], are present at high cytosolic concentration and possess high Ca2+ binding capacity. Direct correlation has been demonstrated between their mucosal concentration and the efficiency of Ca2+ transfer in intestine and uterus under numerous experimental conditions [26, 28, 30]. It is generally accepted that calbindins facilitate the diffusion of intracellular Ca2+ and serve as a Ca2+ buffer needed for cell protection against Ca2+ stress and accompanying apoptotic cellular degradation that is induced by a high intracellular Ca2+ concentration [15, 36, 37]. In our study, we observed an elevated expression of calbindin 28 kDa in the uterus during calcification of an eggshell compared to the magnum (Figure2) and compared to the uterus with no shell in formation (fold difference in expression: 67) in agreement with previous studies [11, 14, 28]. This uterine calbindin 28 kDa is therefore associated with intracellular Ca2+ transport from the basal membrane of the glandular cells to the apical membrane where Ca2+ is extruded into the uterine fluid.
An alternative system in mammals to maintain a low intracellular Ca2+ concentration relies on the endoplasmic reticulum which contributes to Ca2+ homeostasis through its capacity for Ca2+ uptake and storage [38, 39]. The endoplasmic reticulum Ca2+ ATPases (ATP2A1, 2, 3) play an active role in Ca2+ uptake by this organelle (reaching 10 to 100 mM free Ca2+), while maintaining the cytoplasmic concentration at low concentrations of 10-4 mM free Ca2+. Amongst the three isoenzymes (Table2), only ATP2A2 and ATP2A3 were overexpressed in the uterus compared to the magnum. The absence of ATP2A1 expression fits with its predominant localisation in mammalian muscle in contrast to ATP2A2 and ATP2A3 which are expressed in numerous tissues . The overexpression of ATP2A3 in the uterus compared to duodenum suggests a more crucial role of this transporter, the regulation of which remained to be explored.
The inositol 1, 4, 5-trisphosphate receptors (ITPR) are intracellular Ca2+ channels, localised mainly in the endoplasmic reticulum [41, 42] and allowing the release of Ca2+ from this organelle. The three isoforms (ITPR1, 2 3) were overexpressed in the uterus compared to the magnum but were not modified when comparing the presence or absence of calcification. The higher expression of ITPR1 and ITPR 2 in the uterus compared to the duodenum supports our hypothesis concerning their contribution to the regulation of intra-cellular Ca2+. The ryanodine receptors which are involved in muscle excitation-contraction coupling in mammalian tissues  are alternative channels for Ca2+ release from the endoplasmic reticulum. RYR1 expression was revealed in the uterus, but there was no difference between the uterus, magnum or duodenum, suggesting a weak involvement in endoplasmic reticulum Ca2+ release. In conclusion, these observations of high expression of genes encoding ATP2A pumps and ITPR Ca2+ channels involved in Ca2+ uptake and release in endoplasmic reticulum suggest the involvement of this organelle in intracellular Ca2+ buffering in uterine glandular cells.
The last step of uterine Ca2+ trans-epithelial transport is output from the glandular cells, which occurs against a concentration gradient. Ca2+ secretion towards the uterine fluid occurs via an active process, involving the Ca2+ ATPase [7, 32, 43]. This has recently been associated with the PMCA4 (plasma membrane ATPase Ca2+) . Four isoenzymes (ATP2B1, B2, B3 and B4) of PMCAs pumps are identified in mammals . Only three (ATP2B1, B2, B4) are conserved in birds. Each of these were overexpressed in the uterus compared to the magnum (Figure2). ATP2B2 was also overexpressed in the uterus compared to the duodenum, and in presence of the eggshell mineralisation (Figure3) suggesting a more active role in Ca2+ secretion at the uterine level. In contrast, ATP2B1 and ATP2B4 were underexpressed in the uterus compared to duodenum and for ATP2B4 in presence of shell formation. In mammals, it is ATP2B1 which plays a more important role in intestinal Ca2+ absorption [26, 45]. In other bird species, Parker et al.  localized the plasma membrane Ca2+-transporting ATPase 4 (ATP2B4) in the apical membrane of uterine epithelial cells but did not explore the presence of ATP2B2 and its differential expression during calcification. In human osteoblasts, the isoforms 1 and 2 take part in the Ca2+ supply necessary for bone mineralisation whereas the isoform 4 is not detected .
It was observed thirty years ago that the inhibition of Na+ transfer by Na+/K+ ATPase inhibitors considerably reduced Ca2+ secretion into the uterine lumen [9, 17], showing a coupling between uterine Ca2+ secretion and Na+ re-absorption. The uterine absorption of Na+ is revealed by the decreased Na+ concentrations in the uterine fluid observed between the early stage of shell calcification and the end of calcification (Table1). These observations support the hypothesis that Na+/Ca2+ exchangers participate in the uterine Ca2+ secretion. The role of these transporters is clearly established at the mammalian intestinal and renal level . Our study supported this mechanism for Ca2+ secretion in the chicken uterus, as both Na+/Ca2+ exchangers (SLC8A1 and 3) were overexpressed in the uterus compared to the magnum, whereas their expression did not change in the presence or absence of eggshell mineralisation (Figures2 and 3). The mammalian exchangers allow the cell output of one Ca2+ ion against three Na+ ions at the basolateral membrane level. This transport is facilitated by the Na+ gradient, which provides the energy necessary for the Ca2+ output against its gradient [34, 47]. Similarly, the respective Na+ gradient between the cell (12 mM) and the uterine fluid (80 to 144 mM, Table1) may provide the bird uterus with the energy needed for the Ca2+ output towards the uterine fluid at the apical membrane of the glandular cells. Conversely, the unfavourable gradient of Na+ concentrations between blood (140 mM) and glandular cells at the basal membrane level will prevent Ca2+ uptake in the cells by exchange with Na+. Both Na+/Ca2+ exchangers (SLC8A1 and 3) are therefore predicted to be present only in the apical membrane of the uterine glandular cells. The co-expression of the SLC8A1 and 3 genes and of ATP2BX is observed in numerous Ca2+ transporting epithelia [48–51] but their respective involvements in Ca2+ flux has been questioned. Na+/Ca2+ exchangers have a weak affinity for Ca2+, but strong Ca2+ conductance. On the other hand, the Ca2+ ATP2BX pumps have a strong affinity for Ca2+, but a weaker conductance . These data suggest that Ca2+ transport is mainly assured by the Na+/Ca2+ exchangers. In the hen uterus, the inhibition of the Na+/K+ ATPase led to a 60% decrease in Ca2+ transport in vitro or during uterine perfusion [9, 17]. This observation underlines the importance of the Na+/Ca2+ exchangers in the avian uterus.
During eggshell calcification, Na+ is absorbed from the uterine fluid into the blood plasma. This absorption resulting from the predominance of apical to basolateral flux relative to basolateral to apical flux, is partly due to the presence of the Na+/Ca2+ exchangers (SLC8A1 and 3), but a complementary system has been demonstrated by using epithelial Na+ channel blockers . Amiloride-sensitive Na+ channels are essential in various epithelia . Three subunits (SCNN1A, 1B, 1 G) of the Na+ channel are overexpressed in the uterus compared to the magnum and to the duodenum (Figure2), suggesting the involvement of these transporters in Na+ uptake by the uterine glandular cells at the apical membrane. The γ subunit (SCNN1G) was overexpressed during shell calcification in contrast to the α and β subunits (SCNN1A, 1B) suggesting its predominant involvement in the uterus.
In the basolateral membrane, the Na+ glandular cell output towards plasma is active and occurs against a large electrochemical gradient (Table1). This is provided by the Na+/K+ ATPase, which is crucial in all animals for actively transporting Na+ out and K+ into the cell, and for maintaining the membrane potential and active transport of other solutes in intestine, kidney or placenta [34, 53]. Its presence in the avian uterus and crucial role in ionic transfer during shell formation has been demonstrated [8–10, 17]. In situ hybridization in the chicken uterus  showed that only the α1 subunit of Na+/K+ ATPase (ATP1A1), is present in the uterus whereas the α2 and α3 subunits (ATP1A2, A3) are absent. In this study, the α1 subunit (ATP1A1), but also the β1 subunit of Na+/K+ ATPase (ATP1B1), were overexpressed in the uterus compared to the magnum. We also confirmed the overexpression of α1 subunit of Na+/K+ ATPase during the phase of calcification in contrast to the β1subunit of Na+/K+ ATPase, in agreement with Lavelin et al. .
The possibility of an uptake of Na+ from plasma into the uterine glandular cells at the basal membrane via Na+/HCO3- co-transporters (SLC4A4, 5, 7, 10) is discussed in the section addressing HCO3- transfer.
Primers used for RT-PCR and qRT-PCR of ion transporter genes
HCO3- production and transfer
Eggshell mineralisation results from the co-precipitation of Ca2+ and HCO3-. The bicarbonate precursor of the eggshell calcite is mainly derived from the blood carbon dioxide (CO2) which penetrates the uterine glandular cells by simple diffusion through the plasma membrane [2, 19]. Carbonic anhydrases (CAs)  catalyse the hydration of intracellular CO2 to HCO3-, which is secreted into the uterine fluid. In the mammalian gastrointestinal tract, including pancreas, the cellular and membrane bound CAs are key enzymes allowing secretion or reabsorption of large amount of acid across the mucosa or protect epithelial cells from acid injury by secreting bicarbonate [24, 25, 57]. In all mammalian species, the duodenum buffers gastric acid secretion by producing intracellular HCO3- from CO2 at a higher rate than the stomach or distal small intestine. The CO2 originates from intestinal lumen at the duodenal level but is provided from blood plasma via the respiratory system to the uterine tissue . This study showed a larger expression of the cytosolic CA2 and 7 and of the membrane bound CA4 in the chicken uterus than in magnum (Figure2). No difference in expression was observed between the uterus and the duodenum for CA2 and 4. Cytoplasmic CA2 is the predominant CA in the duodenum, playing a major function in the hydration of CO2 to produce HCO3-. Similarly, we propose that CA2 plays a major role in the uterus to provide the carbonate precursor for the eggshell. CA7 is significantly underexpressed in the uterus compared to the duodenum, suggesting a secondary rule in HCO3- uterine production. A major role for CA2 is supported by the overexpression of this CA gene in the presence of eggshell mineralisation, in contrast to CA4 and 7 (Figure3).
The HCO3- produced by CA2 in uterine glandular cells must be then secreted into the uterine fluid to build the eggshell. In mammalian pancreas  and in duodenum  which secrete large amounts of HCO3- towards the lumen, anion HCO3-/Cl- exchangers (SLC4AX) have been located in apical membrane and Na+/HCO3- co-transporters (SLC26AX) at the basolateral membrane [58, 59]. In the bird uterus, there is a strong association between HCO3- secretion and Cl- transport [9, 31] which supports the involvement of HCO3-/Cl- exchangers. The HCO3- flow through the uterine apical membrane is an electrogenic process which is facilitated by output of intracellular Cl-, via an exchanger of the SLC26 electrogenic family [31, 57]. Our study confirmed the expression of a HCO3-/Cl- exchanger (SLC26A9) in the uterus as shown in other epithelial cells . SLC26A9 is suspected to have a role in intestinal HCO3- secretion, in particular to neutralise gastric acidity [60, 61]. Our results showed an overexpression of SLC26A9 exchanger in the uterus compared to the magnum or when the calcification takes place, whereas no variation of expression was observed between the duodenum and the uterus (Figure2). These observations suggest a common mechanism between both tissues and support the hypothesis of the involvement of this transporter in the supply of HCO3- for eggshell calcification. Na+/HCO3- co-transporter genes (SLC4A4, 5, 7, 10; [58, 62]) are also expressed in the uterus and likely contribute to HCO3-transport. SLC4A4, 5, 7 and 10 showed higher expression in the uterus than in the magnum. An overexpression relative to the duodenum is observed only for SLC4A5, the three others being similarly expressed (Figure2). SLC4A7 is underexpressed in the uterus during calcification compared to its absence (Figure3) suggesting that involvement of this transporter is limited during the eggshell calcification process. In mammals, Na+/HCO3- co-transporters mediate the electroneutral movement of Na+ and HCO3- across the plasma membrane . The ionic concentrations in the plasma and uterine glandular cells (Table1) show a favourable concentration gradient for uptake of these ions, supporting the localisation of these transporters in the basolateral membrane of uterine glandular cells to allow HCO3- entry. However, previous studies [2, 19] showed that the majority of HCO3- used for the eggshell came from blood CO2 and only for a minor part from plasma HCO3-. Na+/HCO3- co-transporters (SLC4A4, 5, 10) are likely to have a minor role in HCO3- supply to the uterine glandular cells. The cystic fibrosis transmembrane conductance regulator (CFTR) contributes to fluid secretion from epithelial cells of the lung, pancreas and intestine, as shown in pathological situations associated with impaired fluid production, Cl- and HCO3- secretion due to defective CFTR [63, 64] or in pharmacological studies of reproductive epithelium . Its contribution to HCO3- secretion is unlikely because of the unfavourable gradient or it is possibly indirect through regulation of HCO3- transporters . Its role as a Cl- channel is discussed in the following section on Cl-. Studies using specific inhibitors and measuring Cl- and HCO3- flows are needed to quantify the contribution of HCO3-/Cl- exchangers in HCO3- uterine secretion.
HCO3- production in the glandular epithelial cells, its secretion into uterine fluid and the co-precipitation of CO32- with Ca2+ leads to a progressive acidification of the uterine fluid and of glandular cells [1, 5]. In fact, two H+ are produced for each CaCO3 formed. This metabolic acidosis is partially compensated by hyperventilation by the hen and by an increased renal H+ excretion .
The plasma membrane Ca2+ -transporting ATPases (ATP2B1, 2) of the apical membrane actively extrude Ca2+, as previously mentioned. However several lines of evidence have established that these pumps contribute to H+ re-absorption coupled to Ca2+ secretion [66, 67]. The present study highlights their crucial role in Ca2+ secretion by uterine glandular cells during eggshell formation and therefore in H+ re-absorption from the uterine fluid through the apical membrane. Alternatively, the Na+/H+ exchangers have been shown to contribute to H+ output in the pancreatic duct which also secretes large amount of HCO3-. In a recent transcriptomic study of the uterus (unpublished data, Brionne A, Nys Y and Gautron J), we detected expression of various Na+/H+ exchangers (SLC9A 1, 2, 6, 7, 8, 9), supporting this possibility.
In this study, RT-PCR shows that the V H+ ATPase pump (VAT) is expressed in the bird uterus during calcification. In mammals, this VAT complex is made up of at least 14 subunits and allows transfer of H+ by hydrolysis of ATP [68, 69]. This VAT is present in many membranes of organelles and also frequently in the plasma membranes of renal cells or osteoclasts . VAT is therefore a good candidate for transferring protons to plasma in the hen uterine glandular cell, especially as this VAT was revealed in other species producing CaCO3 biominerals and shown to export H+ during mineralisation [71, 72]. This proton ATPase extrudes H+ across the basolateral membrane of pancreatic duct epithelium  which is secreting high amounts of HCO3- using mechanisms quite similar to uterine glandular cells. Our study reveals overexpression of the VAT subunit B in the uterus, which transfers large amounts of H+ compared with the magnum, where limited amounts of H+ are transferred. The VAT is likely to participate in H+ export from cytoplasm of the uterine cells to the blood plasma across the plasma membrane. The role of CLCN5 in H+ transfer is discussed in the ensuing Cl- section.
The Cl- concentrations decrease from 71 to 45 mM in the uterine fluid (Table1) when comparing the initial and late stage of eggshell calcification in parallel with changes of larger magnitude in Na+ concentrations. The high concentration of these ions observed at the early stage of calcification might result from the large secretions of water, Na+ and Cl- which occurs during the plumping period (hydration of the egg white proteins), 6 to 10 h after ovulation possibly through a paracellular pathway . These water and saline secretions are completed at the initiation of the rapid phase of shell formation, when Na+ and Cl- net fluxes are inversed. The net flux of Cl- is inhibited by acetazolamide, demonstrating the relationship between Cl- transport and HCO3- secretion derived from CAs activity [8, 9, 31], and the involvement of HCO3-/Cl- exchangers of the SLC4 or SLC26 family [57, 62, 73]. Amongst the SLC4Ax HCO3-/Cl- exchangers, we observed no expression of SLC4A8 and there is no evidence of any expression of SLC4A1, 2 or 3 in avian uterine transcriptomic study . The role of SLC26A9 exchanger was previously discussed in the HCO3- section. This exchanger is predicted to be located in the apical membrane of the uterine glandular cells and to contribute to Cl- cell uptake during eggshell calcification as suggested in hens subjected to acetazolamide inhibitors  or in other species [57, 59].
The CLCN2 channel, a family member of the CLCN (Cl- channel), is relatively ubiquitous in epithelial cells and other cellular types [74, 75]. It is considered to participate in various functions such as cellular volume regulation [76, 77], cardiac activity regulation [78, 79] and Cl- trans-epithelial transfer [80, 81]. Our study revealed that the CLCN2 channel is overexpressed in the uterus compared to the magnum or the duodenum (Figure2). The uterine fluid (>45 mM) and intracellular (4 mM) Cl- concentrations are favourable to a Cl- passive entry in uterine glandular cells. In parallel, another Cl- channel, the cystic fibrosis transmembrane conductance regulator (CFTR) could also contribute to Cl- entry in the cell as observed in numerous tissues . In the chicken uterus, the CFTR channel is expressed at a higher level than in the magnum and the duodenum (Figure2). It is also overexpressed in the uterus during eggshell calcification (Figure3). The CLCN2 and CFTR channel are therefore probably expressed in the apical membrane and might contribute to Cl- entry in the cell.
On the other hand, Cl- output could be carried out by CLCN5, another member of CLCN family. Renal proximal tubule cells highly express the V H+ ATPase for acidification of endosomes and electroneutrality is ensured by transfer of Cl- by CLCN5 . The CLCN5 H+/Cl- exchanger  has been localised mainly in organelle membranes but also in the plasma membrane. Our study revealed an overexpression of CLCN5 H+/Cl- in the uterus compared to the magnum, so this channel might contribute to Cl- output through the basal membrane. An alternative would be that Cl- output relies on cation-coupled cotransport as observed in fish or mammals. The SLC12 family consists of Na+-K+-2Cl- cotransporters and of K+-Cl- electroneutral cotransporters, and are expressed either in kidney where they contribute to salt reabsorption, or more ubiquitously being involved in cell volume regulation [82–84]. In the chicken uterus, one Na+-K+-2Cl- cotransporter (SLC12A2) and 4 K+-Cl- cotransporters (SLC12A4, 7, 8, 9) are putative candidate, as expression of these genes is revealed in the chicken uterus transcriptome (unpublished data, Brionne A, Nys Y and Gautron J). In addition, furosemide, a blocker of Na+-K+-2Cl- cotransporters, has been shown to decrease egg shell thickness .
Initial studies on ion transfer in the uterus using physiological and pharmacological approaches provided a preliminary model of ion transfer contributing to the uterine Ca2+ and HCO3- necessary for shell mineralisation (Figure1) [1, 5, 8–10, 17]. The current approaches using knowledge gleaned from the chicken genome sequence and uterine transcriptomic expression data  identified numerous genes encoding putative transporters supplying the mineral precursors of eggshell mineralisation. We have used this information to build a model describing the ion supply mechanisms in the uterus, following a logical sequence for ion transfers for secretion of large amounts of Ca2+ and HCO3- to form the eggshell (Figure4). This work identified 31 genes and related proteins involved in this process. It is consistent with preliminary hypotheses. Our analysis also revealed that analogies exist in the mechanisms of HCO3- secretion by pancreatic duct cells and by duodenum, and to a lower extent with intestinal epithelial cells for Ca2+ movement, even if the Ca2+ flux is reversed between both uterus and duodenum.
Ca2+ secretion through epithelial glandular cells involves TRPV6 Ca2+ channel in the basolateral membrane (cell uptake entry), 28 kDa calbindin (CALB1, intracellular transfer), endoplasmic Ca2+ pumps type 2, 3 (ATP2A2, 3, uptake by endoplasmic reticulum), and inositol trisphosphate receptors type 1, 2, 3 (ITPR1, 2, 3, output from the reticulum). Ca2+ is then extruded from the glandular cells by the membrane’s Ca2+ pumps (ATP2B1, 2) and Ca2+/Na+ exchangers (SLC8A1, 3). The endoplasmic Ca2+ pumps, inositol trisphosphate receptors, and 28 kDa calbindin contribute to maintain a low intracellular free Ca2+ concentration essential for cell survival.
Na+ transport involves three Na+ channels (subunits SCNN1A, 1B, 1 G; uptake in the cell), Na+/Ca2+ exchangers SLC8A1 and 3 (uptake in the cell) and the Na+/K+ ATPase (ATP1A1, ATP1B1, output from the cell).
K+ uptake entry into the cell results from the Na+/K+ ATPase; the K+ channels (KCNJ2, 15, 16 and KCNMA1) contribute to its output release at the apical membrane.
HCO3 - is mainly produced from CO2 by CA2 and to a lesser extent by CA4, and is also provided at a low level from plasma by the Na+/HCO3 + co-transporters (SLC4A4, 5, 10). HCO3 - is exported from the cell through the HCO3 -/Cl- exchanger SLC26A9.
HCO3 - synthesis in the cell and co-precipitation of HCO3 - with Ca2+ in the uterine fluid produces two H+ which are transferred to plasma via the membrane Ca2+ pumps ATP2B1, 2 in the apical membrane and the VAT pump at the basolateral level.
Cl- ions in the uterine fluid enter the cell by the HCO3 -/Cl- exchanger SLC26A9 and by Cl- channels (CLCN2, CFTR uptake in the cells), and might be extruded by Cl-/H+ exchanger (CLCN5), but also by Na+-K+-2Cl- and K+-Cl- cotransporters (SLC12Ax).
This model proposes a large but not exhaustive list of ionic transfer proteins involved in the supply of Ca2+ and HCO3- or in maintaining cellular homeostasis (volume, electroneutrality). The model qualitatively describes putative mechanisms and cellular localisation of the candidates. These hypotheses relying on expression of the genes and on analogies with other tissues that transfer large amount of ions, need to be confirmed using immunochemistry for their cell localisation or by specific inhibition, to establish their relative contribution and understand their interaction and regulation. This avian model where huge amounts of Ca2+ and HCO3- are exported daily following a precise spatial and temporal sequence should contribute to understanding the mechanism and regulation of ionic precursors of CaCO3 and provide insight for other species secreting a CaCO3 biomineral such as coral, molluscs, foraminifera or sea urchins.
Animals handling and housing
The experiment was conducted at the Unité Expérimentale Pôle d'Expérimentation Avicole de Tours (UEPEAT - INRA, Tours, France) according to the legislation on research involving animal subjects set by the European Community Council Directive of November 24, 1986 (86/609/EEC) and under the supervision of an authorized scientist (Authorization # 7323, J Gautron). Forty week old laying hens (ISA brown strain) were caged individually and subjected to a light/dark cycle of 14 hour light and 10 hour darkness (14 L:10D). The hens were fed a layer of mash as recommended by the Institut National de la Recherche Agronomique (INRA). Each cage was equipped with a device for automatic recording of oviposition time.
Collection of laying hens oviduct tissues
Tissue samples (magnum, uterus, duodenum, kidney and gastrocnemius) were harvested in 8 hens while the egg was in the uterus during the active phase of calcification (16–18 hour post-ovulation). Additionally, uterine tissues were collected from 8 birds injected with 50 μg of F2-α prostaglandin during 4 consecutive days to expel the egg before mineralisation had begun (6 to 8 hours post ovulation). All tissue samples were quickly frozen in liquid nitrogen and stored at −80°C until RNA extraction.
Determination of Gallus gallus cDNA sequences involved in mineral supply and design of primers
The list of ion transporters was established using recent transcriptomic data and Gallus gallus databases when available. The transporters not yet identified in chicken were identified using human orthologs in Swiss-Prot/TrEMBL and RefSeq databases. The corresponding human sequences were aligned to Gallus gallus Refseq database using BlastN algorithm an e-value cut-off of 10-20. Primers (Table3), were designed from the Gallus gallus using Mac vector software (MacVector, Cambridge, U.K.). The quality of the primers was tested by virtual PCR for dimerization and specificity using Amplify 3X software .
RNA isolation, reverse transcription and classical
Total RNA was extracted from frozen tissue samples using a commercial kit (RNeasy Mini kit, Qiagen; Courtaboeuf, France) and simultaneously treated with DNase (RNase-free DNase set, Qiagen; Courtaboeuf, France) according to the manufacturer’s procedure. RNA concentrations were measured at 260 nm using a NanodropND 1000 (Thermo Fischer, Wilmington, Delaware, USA). The integrity of RNA was evaluated on a 2% agarose gel and with an Agilent 2100 Bioanalyser (Agilent Technologies, Massy, France). Only RNA samples with a 28S/18S ratio > 1.3 were considered for RT-PCR and qRT-PCR experiments. Total RNA samples (5 μg) were subjected to reverse-transcription using RNase H-MMLV reverse transcriptase (Superscript II, Invitrogen, Cergy Pontoise, France) and random hexamers (Amersham, Orsay, France). PCR was performed using primers (Table3) for 30 cycles at 60°C. The specificity of the PCR reaction was assessed by sequencing of PCR products (Cogenics, Meylan, France), and alignment of the sequences using BLASTN algorithm against the Gallus gallus RefSeq nucleic data bank.
Quantitative RT-PCR (qRT-PCR)
Alternatively, cDNA sequences were amplified in real time using the qPCR Master mix plus for SYBR® Green I assay (Eurogentec, Seraing, Belgium) with the ABI PRISM 7000 Sequence Detection System (Applied Biosystems, France). To account for variations in mRNA extraction and reverse transcription reaction between samples, mRNA levels were normalized either to ribosomal 18S rRNA levels for each sample in the first series of comparison (magnum, uterus, and duodenum) or to TBP (TATA box binding protein) for each samples in the second series of comparison (comparison of expression in the uterus with and without mineralisation). The expression levels of 18S rRNA were measured using TaqMan Universal PCR Master Mix and developed Taq-Man assay for human 18S rRNA (Applied Biosystems, Courtaboeuf, France) as previously validated . The PCR conditions consisted of an uracil-N-glycosylase preincubation step at 50°C for 2 min, followed by a denaturation step at 95°C for 10 min, and 40 cycles of amplification (denaturation for 15 sec at 95°C, annealing and elongation for 1 min at 60°C). A melting curve was carried out from 60 to 95°C for each sample amplified with SYBR® Green. Each run included triplicates of no template controls, standards and samples. Standards correspond respectively to a pool of the magnum, uterus, and duodenum RT products for the first series of experiments and of the uterus with and without mineralisation for the second series of comparison. The threshold cycle (Ct), defined as the cycle at which fluorescence rises above a defined base line, was determined for each sample and cDNA control. A calibration curve was calculated using the Ct values of the cDNA control samples and relative amount of unknown samples were deduced from this curve. The ratio value was calculated for each sample as sample/18 S rRNA in the first comparison (magnum, uterus, and duodenum) or sample/TBP in the second comparison (uterus with and without calcification). The log of the ratio was used for statistical analysis using the 5th version of StatView, software (SAS Institute Inc. Cary, NC). A one-way analysis of variance was performed to detect differences (P < 0.05; 8 replicates/treatment) in gene expression amongst different conditions.
The authors gratefully acknowledge the European Community for its financial support through the RESCAPE project (RESCAPE Food CT 2006–036018), and SABRE program (European Integrating project Cutting-Edge Genomics for Sustainable Animal Breeding Project 016250). VJ thanks the Region Centre and INRA for financial support. We also thank Magali Berges for her technical assistance and Jean Didier Terlot-Brysinne for care of experimental birds. We wish to thank Prof. Maxwell Hincke, Department of Cellular & Molecular Medicine, University of Ottawa, 451 Smyth Road, Ottawa K1H 8 M5, Canada, for his critical reading of the manuscript and constructive remarks.
- Nys Y, Hincke MT, Arias JL, Garcia-Ruiz JM, Solomon SE: Avian eggshell mineralization. Poult Avian Biol Rev. 1999, 10 (3): 143-166.Google Scholar
- Hodges R, Lörcher K: Possible sources of the carbonate fraction of egg shell calcium carbonate. Nature. 1967, 216: 606-610. 10.1038/216606a0.View ArticleGoogle Scholar
- Lippiello L, Wasserman RH: Fluorescent-antibody localization of vitamin-D-dependent calcium-binding protein in oviduct of laying hen. J Histochem Cytochem. 1975, 23 (2): 111-116. 10.1177/23.2.1090646.View ArticlePubMedGoogle Scholar
- Coty WA, McConkey CL: A high-affinity calcium-stimulated atpase activity in the hen oviduct shell gland. Arch Biochem Biophys. 1982, 219 (2): 444-453. 10.1016/0003-9861(82)90176-X.View ArticlePubMedGoogle Scholar
- Sauveur B, Mongin P: Comparative study of uterine fluid and egg albumen in shell gland of hen. Ann Biol Anim Biochim Biophys. 1971, 11 (2): 213-224. 10.1051/rnd:19710203.View ArticleGoogle Scholar
- Common RH: The carbonic anhydrase activity of the hen oviduct. J Agri Soc Univ Coll Wales. 1941, 31: 412-414.Google Scholar
- Pike JW, Alvarado RH: Ca2 + −Mg2 + −activated atpase in shell gland of japanese-quail (Coturnix-coturnix-japonica). Comp Biochem Physiol B. 1975, 51 (1): 119-125.PubMedGoogle Scholar
- Eastin WC, Spaziani E: Control of calcium secretion in avian shell gland (Uterus). Biol Reprod. 1978, 19 (3): 493-504. 10.1095/biolreprod19.3.493.View ArticlePubMedGoogle Scholar
- Eastin WC, Spaziani E: On the mechanism of calcium secretion in the avian shell gland (Uterus). Biol Reprod. 1978, 19 (3): 505-518. 10.1095/biolreprod19.3.505.View ArticlePubMedGoogle Scholar
- Pearson TW, Goldner AM: Calcium-transport across avian uterus - Effects of electrolyte substitution. Am J Physiol. 1973, 225 (6): 1508-1512.PubMedGoogle Scholar
- Nys Y, Mayel-Afshar S, Bouillon R, Vanbaelen H, Lawson DEM: Increases in calbindin D-28 k messenger-Rna in the uterus of the domestic-fowl induced by sexual maturity and shell formation. Gen Comp Endocrinol. 1989, 76 (2): 322-329. 10.1016/0016-6480(89)90164-0.View ArticlePubMedGoogle Scholar
- Striem S, Bar A: Modulation of quail intestinal and egg-shell gland calbindin (Mr 28000) gene-expression by vitamin-D3, 1,25-dihydroxyvitamin-D3 and egg-laying. Mol Cell Endocrinol. 1991, 75 (2): 169-177. 10.1016/0303-7207(91)90232-H.View ArticlePubMedGoogle Scholar
- Nys Y, Zawadzki J, Gautron J, Mills AD: Whitening of brown-shelled eggs: mineral composition of uterine fluid and rate of protoporphyrin deposition. Poult Sci. 1991, 70 (5): 1236-1245. 10.3382/ps.0701236.View ArticlePubMedGoogle Scholar
- Bar A, Striem S, Mayel-afshar S, Lawson DEM: Differential regulation of calbindin-D28K mRNA in the intestine and eggshell gland of the laying hen. J Mol Endocrinol. 1990, 4 (2): 93-99. 10.1677/jme.0.0040093.View ArticlePubMedGoogle Scholar
- Christakos S, Barletta F, Huening M, Dhawan P, Liu Y, Porta A, Peng X: Vitamin D target proteins: Function and regulation. J Cell Biochem. 2003, 88 (2): 238-244. 10.1002/jcb.10349.View ArticlePubMedGoogle Scholar
- Parker SL, Lindsay LA, Herbert JF, Murphy CR, Thompson MB: Expression and localization of Ca2 + −ATPase in the uterus during the reproductive cycle of king quail (Coturnix chinensis) and zebra finch (Poephila guttata). Comp Biochem Physiol A. 2008, 149 (1): 30-35. 10.1016/j.cbpa.2007.09.014.View ArticleGoogle Scholar
- Pearson TW, Goldner AM: Calcium-transport across avian uterus.II. Effects of inhibitors and nitrogen. Am J Physiol. 1974, 227 (2): 465-468.PubMedGoogle Scholar
- Lavelin I, Meiri N, Genina O, Alexiev R, Pines M: Na + −K + −ATPase gene expression in the avian eggshell gland: distinct regulation in different cell types. Am J Physiol Regul Integr Comp Physiol. 2001, 281 (4): R1169-R1176.PubMedGoogle Scholar
- Lörcher K, Zscheile C, Bronsch K: Rate of CO2 and C14 exhalation in laying hens resting and during egg-shell mineralisation after a single injection of NaHC1403. Ann Biol Anim Biochim Biophys. 1970, 10: 133-139.20. 10.1051/rnd:19700612.View ArticleGoogle Scholar
- Consortium ICGS: Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution. Nature. 2004, 432 (7018): 695-716. 10.1038/nature03154.View ArticleGoogle Scholar
- Jonchère V, Rehault-Godbert S, Hennequet-Antier C, Cabau C, Sibut V, Cogburn LA, Nys Y, Gautron J: Gene expression profiling to identify eggshell proteins involved in physical defense of the chicken egg. BMC Genomics. 2010, 11: 57-10.1186/1471-2164-11-57.View ArticlePubMedPubMed CentralGoogle Scholar
- Sauveur B: Electrolyte composition of different zones of egg albumen in 2 breeds of hen. Ann Biol Anim Biochim Biophys. 1969, 9 (4): 563-573. 10.1051/rnd:19690410.View ArticleGoogle Scholar
- Bronner F, Pansu D: Nutritional aspects of calcium absorption. J Nutr. 1999, 129 (1): 9-12.PubMedGoogle Scholar
- Kaunitz JD, Akiba Y: Duodenal carbonic anhydrase: Mucosal protection, luminal chemosensing, and gastric acid disposal. Keio J Med. 2006, 55 (3): 96-106. 10.2302/kjm.55.96.View ArticlePubMedGoogle Scholar
- Flemström G, Allen A: Gastroduodenal mucus bicarbonate barrier: protection against acid and pepsin. Am J Physiol Cell Physiol. 2005, 288 (1): 1-19.View ArticleGoogle Scholar
- Bouillon R, Van Cromphaut S, Carmeliet G: Intestinal calcium absorption: Molecular vitamin D mediated mechanisms. J Cell Biochem. 2003, 88 (2): 332-339. 10.1002/jcb.10360.View ArticlePubMedGoogle Scholar
- Hurwitz S: Calcium homeostasis in birds. Vitam Horm. 1989, 45: 173-221.View ArticlePubMedGoogle Scholar
- Nys Y: Regulation of plasma 1,25 (OH)2D3, of osteocalcin and of intestinal and uterine calbindin in hens. Avian Endocrinology. Edited by: Sharp PJ. 1993, Bristol: Society for Endocrinology, 345-357. 408pGoogle Scholar
- Nys Y: Régulation endocrinienne du metabolisme calcique chez la poule et calcification de la coquille. 1990, Paris: Thèse de Docteur de l’université en Physiologie animale, 162p-6Google Scholar
- Bar A: Calcium transport in strongly calcifying laying birds: Mechanisms and regulation. Comp Biochem Physiol A. 2009, 152 (4): 447-469. 10.1016/j.cbpa.2008.11.020.View ArticleGoogle Scholar
- Vetter AE, O'Grady SA: Sodium and anion transport across the avian uterine (shell gland) epithelium. J Exp Biol. 2005, 208 (3): 479-486. 10.1242/jeb.01409.View ArticlePubMedGoogle Scholar
- Wasserman RH, Smith CA, Smith CM, Brindak ME, Fullmer CS, Krook L, Penniston JT, Kumar R: Immunohistochemical localization of a calcium-pump and calbindin-D28k in the oviduct of the laying hen. Histochemistry. 1991, 96 (5): 413-418. 10.1007/BF00315999.View ArticlePubMedGoogle Scholar
- Wasserman RH, Taylor AN: Vitamin D3-induced calcium-binding protein in chick intestinal mucosa. Science. 1966, 152 (3723): 791-793. 10.1126/science.152.3723.791.View ArticlePubMedGoogle Scholar
- Hoenderop JGJ, Nilius B, Bindels RJM: Calcium absorption across epithelia. Physiol Rev. 2005, 85 (1): 373-422. 10.1152/physrev.00003.2004.View ArticlePubMedGoogle Scholar
- Jande S, Tolnai S, Lawson D: Immunohistochemical localization of vitamin D-dependent calcium-binding protein in duodenum, kidney, uterus and cerebellum of chickens. Histochemistry. 1981, 71 (1): 99-116. 10.1007/BF00592574.View ArticlePubMedGoogle Scholar
- Lambers TT, Mahieu F, Oancea E, Hoofd L, de Lange F, Mensenkamp AR, Voets T, Nilius B, Clapham DE, Hoenderop JG, et al: Calbindin-D-28 K dynamically controls TRPV5-mediated Ca2+ transport. EMBO J. 2006, 25 (13): 2978-2988. 10.1038/sj.emboj.7601186.View ArticlePubMedPubMed CentralGoogle Scholar
- Christakos S, Dhawan P, Benn B, Porta A, Hediger M, Oh GT, Jeung EB, Zhong Y, Ajibade D, Dhawan K, et al: Vitamin D molecular mechanism of action. Ann N Y Acad Sci. 2007, 1116: 340-348. 10.1196/annals.1402.070.View ArticlePubMedGoogle Scholar
- Gorlach A, Klappa P, Kietzmann T: The endoplasmic reticulum: Folding, calcium homeostasis, signaling, and redox control. Antioxid Redox Signal. 2006, 8 (9–10): 1391-1418.View ArticlePubMedGoogle Scholar
- Rossi D, Barone V, Giacomello E, Cusimano V, Sorrentino V: The sarcoplasmic reticulum: An organized patchwork of specialized domains. Traffic. 2008, 9 (7): 1044-1049. 10.1111/j.1600-0854.2008.00717.x.View ArticlePubMedGoogle Scholar
- Periasamy M, Kalyanasundaram A: SERCA pump isoforms: Their role in calcium transport and disease. Muscle Nerve. 2007, 35 (4): 430-442. 10.1002/mus.20745.View ArticlePubMedGoogle Scholar
- Vermassen E, Parys JB, Mauger JP: Subcellular distribution of the inositol 1,4,5-trisphosphate receptors: functional relevance and molecular determinants. Biol Cell. 2004, 96 (1): 3-17. 10.1016/j.biolcel.2003.11.004.View ArticlePubMedGoogle Scholar
- Patterson RL, van Rossum DB, Kaplin AI, Barrow RK, Snyder SH: Inositol 1,4,5-trisphosphate receptor/GAPDH complex augments Ca2+ release via locally derived NADH. Proc Natl Acad Sci USA. 2005, 102 (5): 1357-1359. 10.1073/pnas.0409657102.View ArticlePubMedPubMed CentralGoogle Scholar
- Lundholm CE: DDE-induced eggshell thinning in birds: Effects of p, p'-DDE on the calcium and prostaglandin metabolism of the eggshell gland. Comp Biochem Physiol C. 1997, 118 (2): 113-128.PubMedGoogle Scholar
- Strehler EE, Zacharias DA: Role of alternative splicing in generating isoform diversity among plasma membrane calcium pumps. Physiol Rev. 2001, 81 (1): 21-50.46.PubMedGoogle Scholar
- Howard A, Legon S, Walters JRF: Human and rat intestinal plasma-membrane calcium-pump isoforms. Am J Physiol. 1993, 265 (5): G917-G925.47.PubMedGoogle Scholar
- Kumar R, Haugen JD, Penniston JT: Molecular-cloning of a plasma-membrane calcium-pump from human osteoblasts. J Bone Miner Res. 1993, 8 (4): 505-513.View ArticlePubMedGoogle Scholar
- Philipson KD, Nicoll DA: Sodium-calcium exchange: A molecular perspective. Annu Rev Physiol. 2000, 62: 111-133. 10.1146/annurev.physiol.62.1.111.View ArticlePubMedGoogle Scholar
- Belkacemi L, Bedard I, Simoneau L, Lafond J: Calcium channels, transporters and exchangers in placenta: a review. Cell Calcium. 2005, 37 (1): 1-8. 10.1016/j.ceca.2004.06.010.View ArticlePubMedGoogle Scholar
- Herchuelz A, Kamagate A, Ximenes H, Van Eylen F: Role of Na/Ca exchange and the plasma membrane Ca2 + −ATPase in beta cell function and death. Ann N Y Acad Sci. 2007, 1099: 456-467. 10.1196/annals.1387.048.View ArticlePubMedGoogle Scholar
- Ruknudin AM, Lakattaa EG: The regulation of the Na/Ca exchanger and plasmalemmal Ca2+ ATPase by other proteins. Ann N Y Acad Sci. 2007, 1099: 86-102. 10.1196/annals.1387.045.View ArticlePubMedGoogle Scholar
- Blaustein MP, Juhaszova M, Golovina VA, Church PJ, Stanley EF: Na/Ca exchanger and PMCA localization in neurons and astrocytes - Functional implications. Ann N Y Acad Sci. 2002, 976: 356-366.View ArticlePubMedGoogle Scholar
- Garty H: Molecular-properties of epithelial, amiloride-blockable Na + channels. FASEB J. 1994, 8 (8): 522-528.PubMedGoogle Scholar
- Jorgensen PL, Hakansson KO, Karlish SJD: Structure and mechanism of Na, K-ATPase: Functional sites and their interactions. Annu Rev Physiol. 2003, 65: 817-849. 10.1146/annurev.physiol.65.092101.142558.View ArticlePubMedGoogle Scholar
- Heitzmann D, Warth R: Physiology and pathophysiology of potassium channels in gastrointestinal epithelia. Physiol Rev. 2008, 88 (3): 1119-1182. 10.1152/physrev.00020.2007.View ArticlePubMedGoogle Scholar
- Hebert SC, Desir G, Giebisch G, Wang WH: Molecular diversity and regulation of renal potassium channels. Physiol Rev. 2005, 85 (1): 319-371. 10.1152/physrev.00051.2003.View ArticlePubMedPubMed CentralGoogle Scholar
- Warth R: Potassium channels in epithelial transport. Pflugers Arch. 2003, 446 (5): 505-513. 10.1007/s00424-003-1075-2.View ArticlePubMedGoogle Scholar
- Steward MC, Ishiguro H, Case RM: Mechanisms of bicarbonate secretion in the pancreatic duct. Annu Rev Physiol. 2005, 67: 377-409. 10.1146/annurev.physiol.67.031103.153247.View ArticlePubMedGoogle Scholar
- Romero MF, Fulton CM, Boron WF: The SLC4 family of HCO3- transporters. Pflugers Arch. 2004, 447 (5): 495-509. 10.1007/s00424-003-1180-2.View ArticlePubMedGoogle Scholar
- Dorwart MR, Shcheynikov N, Yang D, Muallem S: The solute carrier 26 family of proteins in epithelial ion transport. Physiol. 2008, 23 (2): 104-114. 10.1152/physiol.00037.2007.View ArticleGoogle Scholar
- Xu J, Henriksnas J, Barone S, Witte D, Shull GE, Forte JG, Holm L, Soleimani M: SLC26A9 is expressed in gastric surface epithelial cells, mediates Cl-/HCO3- exchange, and is inhibited by NH4+. Am J Physiol Cell Physiol. 2005, 289 (2): C493-C505. 10.1152/ajpcell.00030.2005.View ArticlePubMedGoogle Scholar
- Xu J, Song PH, Miller ML, Borgese F, Barone S, Riederer B, Wang ZH, Alper SL, Forte JG, Shull GE, et al: Deletion of the chloride transporter Slc26a9 causes loss of tubulovesicles in parietal cells and impairs acid secretion in the stomach. Proc Natl Acad Sci USA. 2008, 105 (46): 17955-17960. 10.1073/pnas.0800616105.View ArticlePubMedPubMed CentralGoogle Scholar
- Alper SL: Molecular physiology of SLC4 anion exchangers. Exp Physiol. 2006, 91 (1): 153-161.View ArticlePubMedGoogle Scholar
- Choi JY, Muallem D, Kiselyov K, Lee MG, Thomas PJ, Muallem S: Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis. Nature. 2001, 410 (6824): 94-97. 10.1038/35065099.View ArticlePubMedPubMed CentralGoogle Scholar
- Hug MJ, Tamada T, Bridges RJ: CFTR and bicarbonate secretion to epithelial cells. News Physiol Sci. 2003, 18: 38-42.PubMedGoogle Scholar
- Chan HC, Shi QX, Zhou CX, Wang XF, Xu WM, Chen WY, Chen AJ, Ni Y, Yuan YY: Critical role of CFTR in uterine bicarbonate secretion and the fertilizing capacity of sperm. Mol Cell Endocrinol. 2006, 250 (1–2): 106-113.View ArticlePubMedGoogle Scholar
- Niggli V, Sigel E, Carafoli E: The Purified Ca-2+ Pump of Human-Erythrocyte Membranes Catalyzes an Electroneutral Ca-2 + −H + Exchange in Reconstituted Liposomal Systems. J Biol Chem. 1982, 257 (5): 2350-2356.PubMedGoogle Scholar
- Smallwood JI, Waisman DM, Lafreniere D, Rasmussen H: Evidence That the Erythrocyte Calcium-Pump Catalyzes a Ca-2 + −Nh + Exchange. J Biol Chem. 1983, 258 (18): 1092-1097.Google Scholar
- Beyenbach KW, Wieczorek H: The V-type H + ATPase: molecular structure and function, physiological roles and regulation. J Exp Biol. 2006, 209 (4): 577-589. 10.1242/jeb.02014.View ArticlePubMedGoogle Scholar
- Marshansky V, Futai M: The V-type H + −ATPase in vesicular trafficking: targeting, regulation and function. Curr Opin Cell Biol. 2008, 20 (4): 415-426. 10.1016/j.ceb.2008.03.015.View ArticlePubMedGoogle Scholar
- Nishi T, Forgac M: The vacuolar (H+)-atpases - Nature's most versatile proton pumps. Nat Rev Mol Cell Biol. 2002, 3 (2): 94-103. 10.1038/nrm729.View ArticlePubMedGoogle Scholar
- Furla P, Galgani I, Durand I, Allemand D: Sources and mechanisms of inorganic carbon transport for coral calcification and photosynthesis. J Exp Biol. 2000, 203 (22): 3445-3457.PubMedGoogle Scholar
- Bertucci A, Tambutte E, Tambutte S, Allemand D, Zoccola D: Symbiosis-dependent gene expression in coral-dinoflagellate association: cloning and characterization of a P-type H(+)-ATPase gene. Proc Biol Sci. 2010, 277 (1678): 87-95. 10.1098/rspb.2009.1266.View ArticlePubMedPubMed CentralGoogle Scholar
- Chang MH, Plata C, Zandi-Nejad K, Sindic A, Sussman CR, Mercado A, Broumand V, Raghuram V, Mount DB, Romero MF: Slc26a9-Anion exchanger, channel and Na + transporter. J Membr Biol. 2009, 228 (3): 125-140. 10.1007/s00232-009-9165-5.View ArticlePubMedPubMed CentralGoogle Scholar
- Jentsch TJ, Stein V, Weinreich F, Zdebik AA: Molecular structure and physiological function of chloride channels. Physiol Rev. 2002, 82 (2): 503-568.View ArticlePubMedGoogle Scholar
- Duran C, Thompson CH, Xiao Q, Hartzell HC: Chloride Channels: Often Enigmatic, Rarely Predictable. Annu Rev Physiol. 2010, 72: 95-121. 10.1146/annurev-physiol-021909-135811.View ArticlePubMedPubMed CentralGoogle Scholar
- Furukawa T, Ogura T, Katayama Y, Hiraoka M: Characteristics of rabbit ClC-2 current expressed in Xenopus oocytes and its contribution to volume regulation. Am J Physiol. 1998, 274 (2): C500-C512.PubMedGoogle Scholar
- Britton FC, Hatton WJ, Rossow CF, Duan D, Hume JR, Horowitz B: Molecular distribution of volume-regulated chloride channels (ClC-2 and ClC-3) in cardiac tissues. Am J Physiol Heart Circ Physiol. 2000, 279 (5): H2225-H2233.PubMedGoogle Scholar
- Britton FC, Wang GL, Huang ZM, Ye LD, Horowitz B, Hume JR, Duan DY: Functional characterization of novel alternatively spliced ClC-2 chloride channel variants in the heart. J Biol Chem. 2005, 280 (27): 25871-25880. 10.1074/jbc.M502826200.View ArticlePubMedGoogle Scholar
- Huang ZM, Prasad C, Britton FC, Ye LL, Hatton WJ, Duan D: Functional role of CLC-2 chloride inward rectifier channels in cardiac sinoatrial nodal pacemaker cells. J Mol Cell Cardiol. 2009, 47 (1): 121-132. 10.1016/j.yjmcc.2009.04.008.View ArticlePubMedPubMed CentralGoogle Scholar
- Bosl MR, Stein V, Hubner C, Zdebik AA, Jordt SE, Mukhopadhyay AK, Davidoff MS, Holstein AF, Jentsch TJ: Male germ cells and photoreceptors, both dependent on close cell-cell interactions, degenerate upon ClC-2Cl(−) channel disruption. EMBO J. 2001, 20 (6): 1289-1299. 10.1093/emboj/20.6.1289.View ArticlePubMedPubMed CentralGoogle Scholar
- Nehrke K, Arreola J, Nguyen HV, Pilato J, Richardson L, Okunade G, Baggs R, Shull GE, Melvin JE: Loss of hyperpolarization-activated Cl- current in salivary acinar cells from Clcn2 knockout mice. J Biol Chem. 2002, 277 (26): 23604-23611. 10.1074/jbc.M202900200.View ArticlePubMedGoogle Scholar
- Hebert SC, Mount DB, Gamba G: Molecular physiology of cation-coupled Cl- cotransport: the SLC12 family. Pflugers Arch. 2004, 447 (5): 580-593. 10.1007/s00424-003-1066-3.View ArticlePubMedGoogle Scholar
- Adragna NC, Di Fulvio M, Lauf PK: Regulation of K-Cl cotransport: from function to genes. J Membr Biol. 2004, 201 (3): 109-137. 10.1007/s00232-004-0695-6.View ArticlePubMedGoogle Scholar
- Gamba G: Molecular physiology and pathophysiology of electroneutral cation-chloride cotransporters. Physiol Rev. 2005, 85 (2): 423-493. 10.1152/physrev.00011.2004.View ArticlePubMedGoogle Scholar
- Lundholm CE, Bartonek M: Furosemide decreases eggshell thicjness and inhibits 45Ca2+ uptale by asubcellular fraction of eggshell gland mucosa of the domestic-Fowl. Comp Biochem Physiol C. 1992, 101 (2): 317-320. 10.1016/0742-8413(92)90280-K.View ArticlePubMedGoogle Scholar
- Engels WR: Contributing software to the internet - the amplify program. Trends Biochem Sci. 1993, 18 (11): 448-450. 10.1016/0968-0004(93)90148-G.View ArticlePubMedGoogle Scholar
- Gautron J, Murayama E, Vignal A, Morisson M, McKee MD, Rehault S, Labas V, Belghazi M, Vidal ML, Nys Y: Cloning of ovocalyxin-36, a novel chicken eggshell protein related to lipopolysaccharide-binding proteins, bactericidal permeability-increasing proteins, and plunc family proteins. J Biol Chem. 2007, 282 (8): 5273-5286.View ArticlePubMedGoogle Scholar
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