The cell type, cell status and specific localization of Prothymosin α (PTMA) within cells seemingly determine its function. PTMA undergoes 2 types of protease proteolytic modifications that are useful in elucidating its interactions with other molecules; a factor that typifies its roles. Preferably a nuclear protein, PTMA has been shown to function in the cytoplasm and extracellularly with much evidence leaning on pathognomonic status. As such, determination of its cellular distribution under normal physiological context while utilizing varied techniques is key to illuminating prospective validation of its distinct functions in different tissues. Differential distribution insights at normal physiology would also portent better basis for further clarification of its interactions and proteolytic modifications under pathological conditions like numerous cancer, ischemic stroke and immunomodulation. We therefore raised an antibody against the C terminal of PTMA to use in tandem with available antibody against the N terminal in a murine model to explicate the differences in its distribution in brain cell types and major peripheral organs through western blotting and immunohistochemical approaches.
Results
The newly generated antibody was applied against the N-terminal antibody to distinguish truncated versions of PTMA or deduce possible masking of the protein by other interacting molecules. Western blot analysis indicated presence of a truncated form of the protein only in the thymus, while immunohistochemical analysis showed that in brain hippocampus the full-length PTMA was stained prominently in the nucleus whereas in the stomach full-length PTMA staining was not observed in the nucleus but in the cytoplasm.
Conclusion
Truncated PTMA could not be detected by western blotting when both antibodies were applied in all tissues examined except the thymus. However, immunohistochemistry revealed differential staining by these antibodies suggesting possible masking of epitopes by interacting molecules. The differential localization patterns observed in the context of nucleic versus cytoplasmic presence as well as punctate versus diffuse pattern in tissues and cell types, warrant further investigations as to the forms of PTMA interacting partners.
Keywords
Prothymosin αAnti-C terminal antibodyAnti- N terminal antibodyImmunohistochemistryWestern blotting and localization
Background
Prothymosin α (PTMA) is an unstructured, extremely acidic protein (pI 3.5), expressed in a wide variety of cell types. Progressively, research has attested to it as a protein of clinical significance and potential medical use [1, 2]. It is considered a nuclear protein with a potent nuclear localization signal (NLS), albeit reports indicate cytoplasmic and extracellular presence as well, under specific physiological or pathological conditions [3, 4]. It has a highly conserved amino acid sequence among mammals and this together with its wide distribution affirm that it plays an essential role in an organism other than the traditionally attributed role of immune modulation.
Even so, the precise function is still not well understood. Accumulating data point towards both intracellular and extracellular biological functions of PTMA [5–11]. The major intracellular role is associated with cell proliferation. It has been reported that PTMA stimulates cell proliferation by sequestering a repressor of estrogen receptor activity in various cells [12]. Cancer cells are known to be highly proliferative and indeed high expression of intracellular PTMA has been correlated with progression of a number of cancer types including bladder cancer, liver cancer, breast cancer, head and neck cancer, lung cancer, colon cancer, rectal cancer, ovarian cancer, neuroblastoma, prostate cancer and gastric cancer [13–26]. Moreover, PTMA binds to histones, p300 histone acetyl transferase and cAMP response element binding protein (CREB)-binding protein to induce gene transcription [27, 28]. Recent studies have explored the role of intracellular PTMA in acetylation regulation [29].
Further intracellular roles of PTMA include its involvement in cell survival. Nuclear Factor erythroid 2 related factor (Nrf2), a transcription factor that regulates expression of defensive genes such as antioxidant proteins and detoxifying enzymes, is inhibited by Kelch-like ECH-associated protein 1(Keap1). On one hand, PTMA binds to Keap1 to dissociate Keap1-Nrf2 complex thus upregulating the expression of Nrf2 dependent anti-oxidative stress genes [30]. On the other hand, it has been reported in mediating nuclear import of Keap1 to degrade nuclear Nrf2 and thus switch off downstream gene expression suggesting that it is involved in on/off switch of Keap1-Nrf2 system [31]. Moreover, PTMA acts as an anti-apoptotic molecule in the cytoplasm by interacting with Apaf1 to inhibit apoptosome formation [32] and by binding to cytochrome c [33] thereby inhibiting caspase activation. Reports also show that it interacts with p8 (nuclear protein 1), a natively unstructured protein with anti-apoptotic activity much like PTMA, to form a heterodimer complex that could act in concert to regulate the apoptotic cascade [34]. Interestingly however, PTMA undergoes caspase mediated fragmentation in apoptotic cells at two amino-terminal sub-optimal sites and one carboxy-terminal optimal site [35, 36]. Cleavage at the latter site disrupts its nuclear localization and subsequently its intranuclear functioning [37].
Extracellularly, PTMA plays a role in immunomodulation via a pleiotropic mode by stimulating a variety of immune cells including natural killer cells, T cells and lymphokine-activated killer cells-dendritic cells, monocytes and macrophages. The mechanism by which it regulates immune responses is proposed to be through binding to TLR4 on innate immune cells to trigger induction of pro-inflammatory cytokines. Reports also show that the C-terminus of PTMA holds the immunologically active site of the polypeptide [38]. Seemingly, different parts of the molecule are responsible for the different biological functions it exerts.
Reports from our laboratory also show that extracellular PTMA can confer protection to neurons upon ischemic stress by inhibiting necrosis [39]. Cell death that occurs as a consequence of obstructed blood flow in a brain region causes damage to tissues and results in ischemic stroke. Two modes of cell death occur during ischemic stroke: necrosis at the ischemic core and apoptosis several days later at the region that surrounds the core called the penumbra. Necrosis, a rapid and expanding process contributes largely to cell damage but to this end there are no known inhibitors of necrosis. Apoptosis on the other hand can be inhibited by growth factors. Importantly, PTMA was identified as a molecule that can initiate a switch from uncontrollable necrosis to tractable apoptosis in ischemic neurons [40]. Further findings on the neuroprotective role of PTMA revealed neuron-specific extracellular release of the polypeptide following ischemic stress. PTMA was released in a non-classical manner and this release was mediated by its interaction with the cargo protein, S100A13 [41]. The interaction was shown to require the C-terminal region of PTMA. Since astrocytes have intrinsic caspase 3 activity it was postulated that the non-release of PTMA in astrocytes in brain following ischemia was as a result of caspase cleavage of PTMA in its C-terminus thus depriving it the interaction with S100A13. In addition, caspase cleavage of PTMA disrupts its nuclear localization, resulting in redistribution of the polypeptide. PTMA is also capable of proteolytic lysis by asparaginyl endopeptidase in its N-terminus to yield thymosin alpha 1 (TA1) but it still remains to be elucidated if this proteolysis is simply a step in the catabolism of PTMA or a more specific selective process in view of some biological function of TA1 [42].
Depending on the proteins which it interacts with, PTMA exerts different effects; a feature that is determined by its subcellular localization. To individualize PTMA interactions and proteolytic modifications that occur in different tissues, it is a prerequisite to determine its cellular modelling in diverse tissues. The subcellular localization in tissues under normal physiological context has been under reported yet this is a core basis for further elucidation of its interactions and proteolytic modifications under pathological conditions like the various cancer forms, ischemic stroke and immunomodulation mechanisms where it exhibits extensively contrasting roles depending on the pathognomonic status and localization. In the present study, we implore western blotting and immunohistochemical techniques to explore the expression of PTMA and its specific cellular localization in different murine tissues using a set of monoclonal antibodies raised against different epitopes on the polypeptide; the brain being the predominant organ of investigation based on our earlier findings [39–41]. First, we generated a monoclonal antibody against the C-terminal region of PTMA (AntiCT) and employed it in conjunction with the anti N-terminal monoclonal antibody (2 F11) for a comparison. We therefore observe that, the preferential combination of the applied techniques and monoclonal antibodies would lay ground to prospective examinations for better understanding of factors that mediate biological function of PTMA across brain cells and other peripheral tissues not only during proteolytic modifications in pathological conditions but also under normal physiology context.
Methods
Experimental animals
Two female Wistar rats were used for the generation of monoclonal antibodies. Male MP-BL mice were used for the western blotting and immunohistochemistry experiments. The animals were kept in a room maintained at constant temperature (21 ± 2 °C) and relative humidity (55 ± 5 %) with an automatic 12 h light/dark cycle with free access to standard laboratory diet and water ad libitum.
Immunization of animals
Synthetic biotinylated carboxy-terminal peptide of PTMA, (bearing the sequence DDVDTKKQKTEEDD, -Cat.No 293211. GL Biochem Shanghai Ltd), was used as immunogen. Wistar rats were anesthetized and immunized with 200 μg avidin conjugated immunogen, injected on the foot pads as emulsions (1:1 v/v) in complete Freund’s adjuvant (Cat No. 263810, DIFCO Laboratories Detroit, MI) Blood was collected from the immunized animals 2 weeks after the injection and the serum tested for immune reactivity with recombinant mouse PTMA. A week later the animals were sacrificed and the medial iliac lymph nodes aseptically harvested as previously reported [43, 44].
Characterization of the antibody
Hybridomas were prepared using the isolated medial iliac lymph node cells and SP2/0 myeloma cells as the fusion partner in the presence of polyethylene glycol (PEG) and cultured in Hypoxthanthine Aminopterin Thymidine (HAT) selective medium. Cell culture media was then assayed by standard Enzyme linked Immuno-sorbent Assay (ELISA) for the presence of PTMA-reactive antibodies and cells from the ELISA-positive wells cloned by limiting dilution. Screening of hybridoma cell line supernatants was performed via ELISA. Positively identified hybridoma clones were expanded and inspected for monoclonality then assayed by ELISA for immune-reactivity. Desired clones were subsequently re-expanded and adapted to RPMI1640 medium. The monoclonal antibody was then purified from the supernatant by Protein G affinity chromatography and the concentration of purified antibody was determined by Lowry method.
Application of antibody in western blot analysis
Mice were decapitated and the desired brain regions (Olfactory bulb, cortex, amygdala, hippocampus, striatum, cerebellum, thalamus, hypothalamus, mid brain pons and medulla) and tissues (peripheral tissues including spleen, thymus, lung, heart, kidney, liver, colon, stomach, duodenum, jejunum, ileum and cecum) were obtained and transferred into ice-cold homogenizing buffer (20 mM Tris-HCI, pH 7.4, 10 mM NaCl, 1 mM EDTA, 0.01 % SDS, 1 % Triton X-100 and 1X protease inhibitor cocktail) . Tissue lysis was performed using tissue homogenizer or sonication. The homogenate was centrifuged at 15,000 rpm for 30 min at 4 °C. An aliquot of the supernatant was taken for protein quantification, equivalent amounts of total protein mixed with 2 x SDS sample buffer and heated in a boiling water bath for 5 min. The boiled samples were either used immediately or frozen at –20 °C.
Protein quantification of recombinant PTMA and total protein concentration of tissue homogenates was determined by Lowry protein assay method. Samples were prepared for loading onto gel using 1×SDS loading buffer as previously described. Indicated quantities of recombinant Prothymosin α and the tissue samples containing 20 μg of total protein were electrophoresed on 15 % SDS-polyacrylamide gels, transferred onto a nitrocellulose membrane by electroblotting performed at 30 V, 100 mA for 90 min and subjected to immunoblotting with appropriate antibody. In the case of untagged recombinant and tissue PTMA, transfer onto a membrane was by electroblotting with acidic buffer (20 mm sodium acetate buffer, pH 5.2) followed by fixation with 0.5 % glutaraldehyde. Blotted membranes were blocked with 5 % skim milk and 2 % FBS in TBST or 5 % BSA. Membranes were then probed with rat/mouse anti-PTMA (AntiCT and 2 F11 from Alexis Biochemicals respectively) and mouse anti-GAPDH (internal control) primary antibodies followed by Horseradish Peroxidase (HRP)-conjugated goat secondary antibodies. Visualization of immunoreactive bands was executed by enhanced chemiluminescent (ECL). Densitometry of the detected protein bands was determined using ImageJ software. The densitometry ratio of PTMA to GAPDH was calculated. For the purpose of comparison between tissues and between different sets of experiments, the densitometry ratio of each tissue was plotted.
Application of antibody in immunoprecipitation assay
10 μg Protein G sepharose fast flow slurry was incubated with 10 μg of indicated antibody at 4 °C overnight in agitating condition. The beads were then washed 3 times each with wash buffer and incubated with sample (tissue lysate or recombinant protein), at 4 °C for 4 h followed by 3 washes and eluted with 1X SDS loading buffer. Immunoprecipitated samples were then boiled for 5 min and analysed by western blot.
Application of antibody to immunohistochemistry
Mice peripheral tissues and specific brain regions were fixed by vascular perfusion with 30 mL of 4 % paraformaldehyde (PFA) after perfusion with PBS for about 20 min. Desired organs were isolated and washed with PBS then processed using a rapid microwave automatic histo-processor using a standard protocol and embedded into paraffin wax. Subsequent immunohistochemistry assays were then performed per standard protocols previously described [15]. Briefly, sectioned tissues were deparrafinized then permeabilized with methanol. The sections were then blocked with 3 % BSA for 1 h at room temperature and later incubated with primary antibody (1:300 mouse monoclonal IgG 2 F11; Enzo Life Sciences Int., PA, USA and AntiCT)) at 4 °C overnight, washed with PBST then with secondary antibody conjugated to AlexFluor (1:600) for 2 h at room temperature. Counterstaining with Hoechst 33342 (1:10,000) was effected. The slides were then mounted by pristine mount and left to dry overnight at 4 °C. Images were collected by BZ-8000 microscope (KEYENCE, Osaka, Japan) with a × 20 Plan APO lens (Nikon, Tokyo, Japan).
Application of antibody to immunocytochemistry
Primary cortical cells on an eight-well Lab Tek chamber were fixed in 4 % PFA in PBS at 4 °C overnight followed by 3 wash steps with PBS. Fixed cells were permeabilized with 50 and 100 % methanol for 10 min each then washed with PBS 3 times. The permeabilized cells were washed with 0.1 % Triton X-100 in PBS (PBST), incubated in blocking buffer (3 % BSA in PBST) for 3 h at 4 °C, and then incubated in primary antibody (1 : 300; mouse monoclonal IgG 2 F11; Enzo Life Sciences Int., PA, USA and AntiCT) overnight at 4 °C. The cells were then washed with PBST and thereafter incubated in a secondary antibody conjugated to AlexFluor. The nuclei were visualized with Hoechst 33342. Images were collected using a BZ-8000 microscope (KEYENCE, Osaka, Japan) with a × 20 Plan APO lens (Nikon, Tokyo, Japan).
Ethical clearance
All the procedures were formally approved by Nagasaki University Animal Care Committee. The guidelines were strictly adhered to during the research.
Results
Selection of hybridoma cell lines secreting monoclonal antibodies by indirect ELISA was performed using purified Glutathione S- transferase (GST) and Maltose binding protein (MBP) tagged recombinant PTMA as the antigen. From approximately 1500 primary hybridomas 16 yielded immune reactive signals 3-100-fold above background as indicated by optical density (OD) values (data not shown). The 16 hybridomas were all confirmed to react with recombinant PTMA in a second round of ELISA screening. To determine whether the secreted antibodies could specifically detect full-length PTMA, the 16 hybridoma candidates were tested for their reactivity against recombinant mouse PTMA by western blot analysis (Fig. 1). The C-terminal truncated PTMA was included to assay the specific detection of C-terminus region. Supernatant from the hybridoma cell culture was used for the analysis. The antibodies from the cultures could detect full-length PTMA but not the C-terminal truncated one.
Fig. 1
Western blot analysis of hybridoma immune-reactivity MBP and GST tagged recombinant mouse PTMA (as shown in the inlet) were loaded onto gel for electrophoresis and thereafter blotted on to nitrocellulose membranes. Blotted membranes were incubated with supernatant from the hybridoma cultures from different clones as indicated. HRP conjugated anti-rat IgG secondary antibody and HRP substrate was used to develop the bands. Signals were detected by enhanced chemiluminescence. No band was detected on the C-terminal deleted mutant of PTMA (lane 3), while bands corresponding to full-length tagged recombinant PTMA were detected with different intensities across the clones
To further investigate if the generated antibody could detect rat and human PTMA, western blot analysis was carried out using purified recombinant full-length mouse, rat and human Prothymosin α (Fig. 2). Supernatant from the hybridoma culture was used for this analysis. Clones 1, 5 and 7 showed somewhat similar signal intensities for the detection of PTMA across the species. On the other hand, clones 3, 4, 8, 13, 15 and 16 showed higher affinity for mouse PTMA whereas clones 9, 11 and 12 lost their ability to secret the antibodies. Clones 10 and 14 showed relatively very weak signal intensities. PTMA sequence is highly conserved across species (Fig. 3), coloured amino acids denote less conserved sections. While amino termini of all three species show precise homology, the carboxy termini show some differences between the species. Nevertheless, some antibodies from various hybridoma cell lines could recognize the c-terminus of PTMA across species.
Fig. 2
Determination of cross reactivity of the antibodies with rat and human PTMA. GST tagged recombinant mouse, rat and human PTMA were loaded onto gel for electrophoresis and blotted on to nitrocellulose membranes thereafter. Blotted membranes were incubated with supernatant from the hybridoma cultures from different clones as indicated. Antibodies from most clones showed crossreactivity with rat and human PTMA. Some showed relatively similar or different signal intensities indicative of the affinity of the antibodies to the particular antigens. Clones 9, 11 and 12 lost their ability to secret antibodies
Fig. 3
Alignment of amino acid sequences of human, rat and mouse Prothymosin alpha
Clone 7 (Figs. 1 and 2) was selected for further culture due to its consistency in PTMA detection after cloning. The selected clone was adapted to RPMI1640 medium and antibody immunoreactivity confirmed. The hybrodoma clone was then grown in serum free GIT medium and the secreted antibodies were purified by protein G affinity chromatography, dialyzed with PBS and later antibody concentration was determined. Reactivity of the purified antibody was assayed by western blotting and antibody tested for capacity to immunoprecipitate PTMA from tissue and the recombinant PTMA. AntiCT antibody successfully immunoprecipitated PTMA from the cerebellum tissue lysate. Anti N-terminal PTMA (2 F11) was applied alongside AntiCT in the immunoprecipitation studies for a comparison. Detection of PTMA immunoprecipitated by both antibodies was carried out by 2 F11. Same amount of antibody was used for each antibody type. 2 F11 antibody showed greater capacity for immunoprecipitation than AntiCT.
The tissue-wide distribution of PTMA was assessed using the newly generated anti C-terminal PTMA (AntiCT) and the anti N-terminal PTMA (2 F11) antibodies. To explore whether proteolytically modified forms of PTMA could be detected by the set of antibodies, the immunoblot assay was performed in brain regions and peripheral tissues. Immunoblot data revealed a single band detectable by both 2 F11 and AntiCT that corresponded to full-length PTMA in the brain regions (Fig. 4), no additional bands were detected indicative of proteolytic modification of PTMA. In peripheral tissues, a similar observation was made (Fig. 5), however an additional lower band was detectable by 2 F11 only in the thymus suggesting c-terminal truncated version o or several different variants of PTMA could be present. The relative levels of PTMA in different tissues were calculated according to densitometry measurements and the data are summarized. Densitometric quantification of the western blot bands of PTMA expression across peripheral tissues and selected brain regions [Additional files 1 and 2 correspondingly] corresponding to Figs. 4 and 5 respectively. In the brain, the highest levels of PTMA were detected in the olfactory bulb and cerebellum by both antibodies while in peripheral tissues, the thymus, spleen and lungs showed high PTMA levels by both antibodies. Relatively low PTMA levels were detected in the heart, kidney and liver.
Fig. 4
Western blot analysis of the distribution of PTMA in selected brain regions. Immunoreactive PTMA from regions of the brain tissue shows single bands at apparent molecular weight of 12 kDa. Lysates from multiple sections of the brain were resolved in electrophoretic gel and transferred to nitrocellulose membranes. The western blot analysis was performed with monoclonal 2 F11 and monoclonal AntiCT. Untagged recombinant PTMA was used as positive control and GAPDH as internal control
Fig. 5
Western blot analysis of the distribution of PTMA across peripheral tissues. Immunoreactive PTMA from various peripheral tissues shows single bands at apparent molecular weight of 12 kDa. Lysates from the peripheral tissues were resolved in electrophoretic gel and transferred to nitrocellulose membranes. The western blot analysis was performed with monoclonal 2 F11 and monoclonal AntiCT. GAPDH was used as internal control
PTMA localization was evaluated by immunohistochemistry in a spectrum of organs Multi-colour experiment was performed for PTMA visualization by co-staining with AntiCT and 2 F11 antibodies. Hoechst stain was used to visualize the nucleus. We observed a differential staining pattern among the tissues examined. Immunoreactivity of PTMA was mainly in the nucleus of most tissues, while other tissues indicated predominant cytoplasmic staining. In the hippocampus PTMA signals were intense in the nucleus (Fig. 6a iii) when detected by both Anti CT and 2 F11 (Fig. 6a i and ii) clearly indicated by the merge data (Fig. 6a iv). In the lungs, an intriguing observation was made in the pattern of distribution of PTMA expression. The AntiCT antibody stained both nucleus and cytoplasm (Fig. 6b i iii and iv) in majority of the cells while 2 F11 stained only the cytoplasm in most cells and the perinuclear space in few cells (Fig. 6b ii, iii and iv).
Fig. 6
Immunohistochemistry analysis of PTMA in (a) mouse brain hippocampus tissue and (b) Lung tissue. Whole animal vascular perfusion fixation was conducted with PFA and the required tissues were isolated. The brain hippocampus and lung were processed for immunohistochemistry by embedding to paraffin wax. Tissue sections were stained with AntiCT (a)i and (b)i and 2 F11 (a)ii and (b)ii together with relevant fluorescent tagged antibodies. Sections were then washed, counterstained with Hoechst (a)iii and (b)iii and processed for fluorescence microscopy. Both antibodies localized PTMA in the nucleus of the hippocampus (a)i and ii, while in the lung PTMA immunoreactivity was observed in the nucleus and cytoplasm by AntiCT (b)i but mainly in the cytoplasm by 2 F11 (b)ii
The heart presented weak PTMA immunostaining by both AntiCT and 2 F11 antibodies (Fig. 7a i, ii and iii) and clearly illustrated by the merge (Fig. 7a iv) in correlation with the western blot data that indicated weak PTMA expression. In the kidney, PTMA was primarily expressed in the nucleus (Fig. 7b iii) by both antibodies (Fig. 7b i and ii) with AntiCT showing more intense signal (Fig. 7b iv).
Fig. 7
Immunohistochemical examination of PTMA in (a) mouse heart and (b) kidney tissue. Whole animal vascular perfusion fixation was conducted with PFA and the required tissues were isolated. The heart and kidney were processed for immunohistochemistry by embedding to paraffin wax. Tissue sections were stained with AntiCT (a)i and (b)i and 2 F11(a)ii and(b)ii together with relevant fluorescent tagged antibodies. Sections were then washed, counterstained with Hoechst (a)iii and(b)iii) and processed for fluorescence microscopy. The heart PTMA immunoreactivity was moderate by both antibodies (a)i and ii. The kidney AntiCT showed higher immunofluorescent intensity in comparison to 2 F11 signals in the Kidney (b)i and ii
In the liver PTMA was demonstrated considerably in the nucleus (Fig. 8b iii) by both AntiCT ant 2 F11 (Fig. 8a i, ii and iv), this correlates with the western blot data that showed substantial expression of PTMA. In the stomach, PTMA immunoreactive cells of the mucosal layer demonstrated quite a unique distribution pattern. PTMA was not stained in the nucleus (Fig. 8b iii) of these cells by either of 2 F11 or AntiCT antibodies (Fig. 8b i and ii). Interestingly, only the cytoplasm was positively immunostained, clearly indicated by the merge data (Fig. 8b iv). Showing both antibodies exhibited strong cytoplasmic immunofluorescent intensity.
Fig. 8
Immunohistochemical examination of PTMA expression levels in (a) mouse liver tissue and (b) stomach. Whole animal vascular perfusion fixation was conducted with PFA and the required tissues were isolated. The liver and stomach were processed for immunohistochemistry by embedding to paraffin wax. Tissue sections were stained with AntiCT (a)i and (b)i and 2 F11 (a)ii and (b)ii together with relevant fluorescent tagged antibodies. Sections were then washed, counterstained with Hoechst (a)iii and (b)iii and processed for fluorescence microscopy. The liver shows substantial nucleic PTMA immunoreactivity by both antibodies (a)i and ii whereas only the cytoplasm showed immunofluorescence by both 2 F11 and AntiCT in the stomach (b)i and ii
The duodenum showed PTMA immunoreactivity in the nucleus (Fig. 9a iii) and weakly in the cytoplasm but AntiCT (Fig. 9a i) demonstrated higher signal intensity than 2 F11 (Fig. 9a ii). Additionally, 2 F11 depicted perinuclear staining in some submucosal layer cells. The jejunum also presented an exceptional PTMA staining pattern in which the AntiCT shows immunoreactivity mainly in the nucleus (Fig. 9b i and iii) while 2 F11 depicts mainly a cytoplasmic immunostaining (Fig. 9b ii). Some cells show perinuclear staining with 2 F11 only, while few show perinuclear staining with both antibodies (Merge, Fig. 9b iv).
Fig. 9
Immunohistochemical analysis of PTMA in (a) mouse duodenum and (b) Jejunum. Whole animal vascular perfusion fixation was conducted with PFA and the required tissues were isolated. The duodenum and jejunum were processed for immunohistochemistry by embedding to paraffin wax. Tissue sections were stained with AntiCT (a)i and (b)i and 2 F11 (a)ii and (b)ii together with relevant fluorescent tagged antibodies. Sections were then washed, counterstained with Hoechst (a)iii and (b)iii) and processed for fluorescence microscopy. In the duodenum, PTMA immunoreactivity revealed nucleic staining with AntiCT (b)i and cytoplasmic staining with 2 F11 (b)ii
Ileum, colon and cecum demonstrated a similar pattern of distribution of immunoreactive PTMA (Figs. 10a, b and 11 respectively). The AntiCT stained with much higher fluorescent intensity (Figs. 10a i, iii; b i, iii and Fig. 11 i, iii), depicting strong nucleus signal compared to cytoplasmic signal. 2 F11 showed moderate nucleus signal (Figs. 10a ii, iii; b ii, iii and Fig. 11 ii, iii). An overlay of PTMA and nuclear staining is shown in the merge data (Figs. 10a, b and 11iv).
Fig. 10
Immuohistochemical analysis of PTMA in (a) mouse ileum tissue and (b) colon. Whole animal vascular perfusion fixation was conducted with PFA and the required tissues were isolated. The ileum and colon were processed for immunohistochemistry by embedding to paraffin wax. Tissue sections were stained with AntiCT (a)i and (b)i and 2 F11 (a)ii and(b)ii together with relevant fluorescent tagged antibodies. Sections were then washed, counterstained with Hoechst (a)iii and(b)iii and processed for fluorescence microscopy. The ileum and colon depict nucleic PTMA staining with AntiCT (a and b)i and cytoplasmic staining with 2 F11 (a and b)ii
Fig. 11
Immuohistochemical examination of PTMA in cecum. The cecum was processed for immunohistochemistry by embedding to paraffin wax. Tissue sections were stained with AntiCT (i) and 2 F11 (ii) together with relevant fluorescent tagged antibodies. Sections were then washed, counterstained with Hoechst (iii) and processed for fluorescence microscopy. Some cells showed PTMA immunoreactivity in both nucleus and cytoplasm with both antibodies while others show nucleus staining with AntiCT and cytoplasmic staining with 2 F11 (i and ii)
Given that PTMA has previously been shown by 2 F11 to be exclusively located in the nuclei of neurons we explored cell-type specific distribution of PTMA: an immunocytochemical study, by immunostaining with newly generated anti C-terminus PTMA antibody whether a similar staining pattern would be observed. We used primary cortical neurons cultured from 17 day-old embryonic rat brain. Anti C-terminal PTMA depicted a punctate signal that was widely distributed throughout the nucleus; weak signals were also detected in the cytoplasm as by the arrow heads shown (Fig. 12), eliciting contrast with the 2 F11 antibody.
Fig. 12
Cellular distribution of PTMA in rat primary neurons. Fixed rat primary cortical neuron cells were permeabilized with 50 and 100 % methanol then washed with PBS. The permeabilized cells were incubated in blocking buffer, and then with AntiCT (a)i and 2 F11(b)ii. Stained cells were then processed for fluorescence microscopy. C-terminal antibody stained PTMA in the primary cortical neurons with a punctate pattern while anti N-terminal showed diffuse nuclear staining. Arrowheads denote the weak cytoplasmic signals detected by the anti C-terminal PTMA antibody only
Discussion
Prothymosin α (PTMA) generates a great deal of interest among investigators due to its robust involvement in a variety of biological processes ranging from cell proliferation as observed in several types of cancer [13–26] and apoptosis [34, 37, 39, 40, 45] to its association with cell-mediated immunity [6, 8, 46]. Moreover, going by recent studies conducted to understand the role PTMA in non-mammalian vertebrates, insights into changes in PTMA functions and expression that have occurred with evolution is required. It has been shown that PTMA is involved in spermatogenesis in the frog [47, 48] and in the cartilaginous fish Torpedo marmorata [49]. In the zebrafish, the PTMA gene has been shown to be duplicated [50] and expressed differentially during embryonic development indicating that their function is more complex in fishes than in mammals.
As yet, its subcellular localization in tissues under normal physiological context has been underreported equally utilizing narrow range techniques. In the present study we demonstrated the tissue distribution and subcellular localization of PTMA in diverse murine organ tissues and cell types. The insights into its differential dissemination in brain cell types and major peripheral organs at normal physiology, would portent better basis for further elucidation of its interactions and proteolytic modifications under pathological conditions. This considers the fact that, it exhibits extensively contrasting roles depending on the pathognomonic status and localization as either intracellular or extracellular. To illuminate the differential distribution and localization of PTMA, with respect to different tissues and cell types, antibodies that discriminate the different epitopes on the polypeptide were useful tools. First we developed an antibody against the C-terminus of PTMA, a region that presents relatively high hydrophilicity and mobility indices and is therefore likely to have high antigenicity, according to a previous theoretical evaluation [51]. Additionally, antigenic determinants of polypeptides are usually located in their N and/or C termini therefore the C-terminus of PTMA is putatively immunogenic. The rat iliac lymph node method was utilized to produce the monoclonal antibodies instead of the conventional spleen method as it offers a number of benefits; (a) a single injection is sufficient for immunization, (b) lymph nodes are ready to use 2 weeks after injection and (c) increase in efficiency (10 times higher than conventional method) due to higher yield of positive hybridomas. In this method, biotinylated C-terminal peptide of PTMA was used as antigen and emulsified with complete Freund’s adjuvant. Rats were immunized once and 3 weeks later lymphocytes from the iliac lymph nodes of immunized rats were fused with SP2/0 myeloma cells. Antibody producing hybridomas were screened by ELISA and 16 positive clones were selected. On assaying reactivity of the purified antibody by western blotting and antibody testing for capacity to immunoprecipitate PTMA from tissue and the recombinant PTMA, it was evident that AntiCT antibody successfully immunoprecipitated PTMA from the cerebellum tissue lysate. When Anti N-terminal PTMA (2 F11) was applied alongside AntiCT for comparison and detection of PTMA immunoprecipitated by both antibodies carried out by 2 F11 using same amount of antibody for each antibody type; 2 F11 antibody showed greater capacity for immunoprecipitation than AntiCT. It is worth noting that the presence of variant proteins with the same N-terminal sequence generated from alternative splicing of the PTMA gene as recently reported [46] would possibly account for this difference. This observation needs to be verified in further prospective investigations.
The applied methodology revealed that the generated antibody was able to recognize full-length PTMA but could not detect the C-terminal truncated mutant as shown by the western blot results therefore, demonstrating the specificity of the antibodies to the C-terminal region of PTMA. Further characterization of the antibody by determining its cross reactivity with rat and human PTMA revealed clones with different species-specific affinities for PTMA while some clones lost the ability to secrete the antibodies possibly due to loss of chromosomes. Taken together, these results indicated successful generation of the C-terminal antibody. For subsequent experiments purified antibody from clone 7 (AntiCT) was used. A previous study by our laboratory showed that PTMA is a unique cell death regulatory molecule and therefore has neuroprotective roles in brain stroke [39, 45]. Additional studies demonstrated that PTMA exerts the neuroprotective function via its extracellular release upon interaction with S100A13 and that the C-terminal region of PTMA is required for this interaction [41]. However, PTMA cleavage by caspase in its C-terminus interferes with the interaction with S100A13 and disrupts its nuclear localization. Concurrently, PTMA undergoes asparaginyl endopeptidase-mediated cleavage in its N-terminus [42]. Such proteolytic modifications could present functional discontinuities of PTMA and aid to unearth other macromolecules that participate in PTMA functions. Therefore, we first investigated the presence of proteolytically modified variants of PTMA in mouse tissues by western blotting. When AntiCT was applied against 2 F11 in the immunoblot assay, a differential PTMA distribution pattern was observed in the brain regions and peripheral tissues. The tendency of PTMA expression pattern was similar by both antibodies, depicting a trend of high expression levels in brain regions associated with high neuron population (cerebellum) and regions in which neurogenesis is known to occur (olfactory bulb and hippocampus). Brain regions that showed the lowest levels include the thalamus and cortex. Only a single band signal was detectable, cleaved forms of PTMA were undetectable in brain region. In peripheral tissues PTMA expression was higher in lymphoid tissues such as thymus and spleen and lowest in the liver, only the thymus registered an additional lower band signal when detected by 2 F11 which was undetectable by AntiCT. It is plausible that this lower molecular weight band is indeed the C-terminal cleaved form of PTMA owing to the fact that the thymus is packed with apoptosing cells as a result of high cell turnover in this tissue. Further experiments will help to unequivocally determine the identity of the lower band. Overall, the expression level of cleaved forms of PTMA was undetectable in all tissues tested except the thymus under normal physiological context. It would be interesting to explore this phenomenon after induction of some stress. Following the revelation of the PTMA expression trend in the various tissues, we explored the subcellular localization by use of immunohistochemistry techniques.
Immunohistochemical analysis was performed by co-staining with both antibodies (AntiCT and 2 F11). Immunostaining with AntiCT revealed that in most of the tissues analyzed, the expression of PTMA was localized in both the nucleus and cytoplasm while PTMA immunoreactivity was mostly detected in cytoplasm or perinuclear space by 2 F11. Specific cells of the mucosal layers of duodenum, jejunum, ileum, colon and cecum corroborated this observation. Some cells in the submucosal layers of the duodenum and cecum showed PTMA immunoreactivity in the perinuclear space only by both antibodies. It is conceivable that this differential subcellular localization of PTMA is as a result of different PTMA interacting molecules in the different tissue and cell types or proteolytic modification of PTMA, however no PTMA cleaved forms were detected in these tissues. The brain hippocampus and stomach tissue sections revealed interesting staining patterns that differed from the aforementioned tissues. On one hand, exclusive nuclear staining of PTMA was observed in the hippocampus by both antibodies and on the other hand exclusive cytoplasmic staining was observed in the stomach when both antibodies were applied. As PTMA plays multiple cell robustness roles, this specified subcellular localization in the hippocampus and the stomach by both AntiCT and 2 F11 suggests cell type specific functioning of PTMA. The expression intensity in other tissues like the liver and the heart was relatively weak while the kidney showed comparatively higher signal intensity by immunohistochemistry where the signal was mainly localized in the nucleus. Interestingly the immunofluorescence detected in the lung tissues showed both nucleus and cytoplasmic staining by AntiCT but only cytoplasmic staining by 2 F11. This could be attributable to an interacting molecule involving the N-terminal of PTMA in the nucleus of lung cells. To determine the pattern of cellular distribution of PTMA in detail, immunocytochemistry analysis was carried out on primary neurons. As observed, AntiCT depicted a punctate distribution pattern in the nucleus of neurons and weakly stained the cytoplasm, features that differed from immunostaininng with 2 F11 which only stained the nucleus diffusely. We could consider the prospect that the punctate pattern detectable by AntiCT in primary neurons is a product of interacting molecules in the nucleus that mask C-terminal region and that the weak cytoplasmic signal detectable by AntiCT but not 2 F11, could indicate presence of interacting molecules in the cytoplasm that engage the N-terminal region of PTMA therefore masking it from detection by 2 F11. All together these expression patterns seem to suggest functional differences of PTMA in diverse tissues and cellular compartments likely associated with different interacting proteins. Under apoptotic conditions intact intracellular PTMA can be processed by proteases leading to different fragments that may differ in biological functions as showed by PTMA-S100A13 binding studies, it would therefore be significant to examine subcellular localization of PTMA under such varying conditions. Moreover, we cannot rule out possibility of the presence of PTMA variants with similar N-terminal regions but differing C-terminal compartments resulting from alternative splicing. Further prospective studies are required to confirm such possible effect.
Conclusion
By analyzing how PTMA is distributed and localized in tissues and specific cell types under no pathological condition we have triggered prying into its precise role under such normal conditions given that in some tissues it was exclusively localized in the cytoplasm while in other tissues it was present predominantly in the nucleus. This will improve our understanding of mediators of PTMA biological function during disease. The next course of action would be to determine the particular cell types that express PTMA in the tissues that showed contrasting patterns of PTMA localization like the cells of the stomach, determine PTMA interacting partners and explore the biologic consequences of PTMA variants in same or different cells arising from alternative splicing.
Abbreviations
2 F11:
antibody against the N-terminal region of prothymosin α
AntiCT:
antibody against the C-terminal region of prothymosin α
CREB:
cAMP response element binging protein
ECL:
enhanced chemiluminescent
ELISA:
Enzyme linked Immuno-sorbent Assay
HAT:
Hypoxthanthine-Aminopterin-Thymidine
HRP:
Horseradish Peroxidase
Keap1:
Kelch-like ECH-associated protein 1
NLS:
Nuclear Localization Signal
Nrf2:
Nuclear Factor erythroid 2 related factor
OPD:
O-phenylenediamine
PBS:
Phosphate Buffered Saline
PEG:
Polyethylene Glycol
PFA:
Paraformaldehyde
PTMA:
Prothymosin α
TA1
:
Thymosin Alpha1
Declarations
Acknowledgements
The authors thank Ms. Maeda Shiori and Mr. Takehiro Mukae of Nagasaki University for technical assistance during data analysis support in the different facets of this study. This study was partially supported by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology (MEXT).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Authors’ Affiliations
(1)
Department of Molecular Microbiology and Immunology, Division of Immunology, Graduate School of Biomedical Sciences, Nagasaki University
(2)
African Population and Health Research Center (APHRC)
(3)
Institute of Tropical Medicine and Infectious Diseases-KEMRI (ITROMID-KEMRI)
(4)
Department of Pharmacology and Therapeutic Innovation, Graduate School of Biomedical Sciences, Nagasaki University
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