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The epigenetic factors causing competence differences between SN (surrounded nucleolus) and NSN (non-surrounded nucleolus) oocytes, the significance for the increased histone acetylation and methylation in SN oocytes, and whether chromatin configuration or histone modification determines oocyte competence, are unclear. This study has addressed these issues by using the ovary-holding (OH) stress models where oocyte SN configuration was uncoupled from histone modifications and developmental potential. Prepubertal mouse ovaries containing high percentages of NSN oocytes were preserved at 37 or 39°C for 1 or 2h before examination for oocyte chromatin configuration, developmental competence, histone modification and apoptosis. Whereas 1-h OH at 37°C caused a moderate apoptosis with increased oocyte competence, improved histone modification and a normal NSN-to-SN transition, harsher OH conditions induced a severe apoptosis with decreased oocyte competence, impaired histone modification and a pseudo (premature) NSN-to-SN transition. Observations on Fas/FasL expression and using the gld (generalized lymphoproliferative disorder) mice harboring FasL mutations indicated that OH triggered oocyte apoptosis with activation of the Fas signaling. It was concluded that OH stress caused oocyte apoptosis with activation of the Fas/FasL system and that oocyte competence was more closely correlated with histone modification than with chromatin configuration.
With the growth of germinal vesicle (GV) stage mouse oocytes, their chromatin configuration changes from the non-surrounded nucleolus (NSN) pattern to the surrounded nucleolus (SN) pattern. While the NSN oocytes have diffuse chromatin, which does not form a heterochromatin rim around the nucleolus, the SN oocytes show condensed chromatin that is particularly confined around the nucleolus1,2,3,4. It seems that oocyte competence is influenced primarily by epigenetic factors that control overall gene expression and significantly modify GV chromatin configuration5,6,7,8. For example, fully-grown oocytes must end an NSN configuration before gaining full meiotic competence, and they must take on an SN configuration and stop gene transcription before being capable of blastocyst formation6. However, the mechanisms for the NSN-to-SN transition are largely unknown and the epigenetic factors causing the difference in developmental competence between NSN and SN oocytes remain to be clearly specified9.
Generally, histone acetylation leads to chromatin relaxation and thus correlates with gene activation, whereas histone deacetylation leads to chromatin condensation and therefore correlates with gene repression10. According to this rule, the core histone tails of GV chromatin should be less acetylated in SN than in NSN oocytes, because chromatin condenses and gene expression is silenced during oocyte growth. However, the level of histone acetylation in SN mouse oocytes was higher than that in NSN oocytes11,12,13. Furthermore, an increase in dimethylated H3K4 and H3K9 has been observed during the growth of mouse oocytes12, but its relationship with the NSN-to-SN transition of chromatin configuration and oocyte competence is unclear. Thus, the significance for the oocyte growth-associated increase in histone acetylation and methylation and its relationship with oocyte chromatin configuration and competence are unknown. Because it is impossible to observe such relations during normal oocyte growth/maturation, models where the SN configuration can be uncoupled from histone modification and oocyte competence must be used for such studies.
Our recent study showed that restraint of mice impaired the NSN-to-SN transition, histone acetylation and methylation in SN oocytes and oocyte developmental potential14. However, whereas the SN percentage of stressed oocytes returned to normal, neither the level of histone acetylation and methylation in SN oocytes nor the developmental competence recovered following a post-restraint recovery. Although these results suggested that the SN configuration was uncoupled from increased histone acetylation and methylation in the restraint-stressed oocytes, and that the developmental potential of SN oocytes is more closely correlated with epigenetic histone modification than with chromatin configuration, the conclusions need further verification using other models. Ovary holding (OH) either below body temperature15 or at a high temperature16 tended to increase SN configurations of oocytes. However, while the former induced early atretic changes and gave rise to more competent oocytes17, the latter totally abolished oocyte competence of maturation in vitro16. Thus, OH stress might be used to study the relationship between chromatin configuration, histone modification and competence of the SN oocytes, because the SN configuration is uncoupled from their developmental competence in the heat-stressed oocytes. Furthermore, why restraint stress inhibited while OH stress facilitated the NSN-to-SN transition, and how the early atretic changes triggered by the low temperature OH and other stressors18,19 improve oocyte competence, need further investigations.
Although observations suggest that the SN configuration represents a stage of GV oocyte that is more advanced toward ovulation, the possibility that this configuration could represent a step toward atresia has also been indicated in some reports4,6. We thus suspected that OH at a high temperature might have induced oocyte apoptosis with a pseudo NSN-to-SN transition reminiscent of the nuclear pyknosis in apoptotic somatic cells20,21, and the resulting configuration with condensed chromatin might have been mistaken as a “SN” configuration in previous reports16. On the other hand, the early atretic changes induced by the low temperature OH and other stressors might have improved oocyte competence by promoting a normal NSN-to-SN transition and improving histone modification.
Fas-mediated apoptosis plays a major role in the induction of apoptosis22,23,24. One recent study indicated that cumulus cells surrounding the aging oocyte released sFasL, which facilitated oocyte aging by binding to Fas receptors on the oocyte25. Furthermore, activation of the Fas pathway during in vitro maturation increased the incidence of apoptosis in cumulus cells of bovine oocytes26. Thus, it is worth studying whether the Fas/FasL system plays any role in the OH stress-induced apoptosis of ovarian oocytes.
We thus hypothesized that OH stress would trigger apoptosis of ovarian cells and oocytes by activating the Fas/FasL system. Whereas a moderate apoptosis induced by milder stresses would improve oocyte competence by facilitating a normal NSN-to-SN transition and improving histone modification, severe apoptosis induced by harsher stresses would decrease competence by inducing a pseudo (premature) NSN-to-SN transition and by impairing histone modification. The aim of this study was to test this hypothesis by OH of prepubertal mouse ovaries from both wild-type mice and the gld (generalized lymphoproliferative disorder) mice harboring FasL mutations. The prepubertal mouse ovaries without equine chorionic gonadotropin (eCG) priming were used because previous studies have shown that whereas adult mouse ovaries contain few, the prepubertal mouse ovaries contain many NSN oocytes before eCG treatment27. The FasL in gld mice carries a point mutation in the C-terminal region, and the recombinant gld FasL can not induce apoptosis in cells expressing Fas28. This suggests that the gld mice can be used as models to study roles of the Fas signaling in stress-induced apoptosis of ovarian cells.
Oocytes from newly recovered ovaries before OH showed 3 patterns of chromatin configuration. In the NSN pattern, chromatin was the least condensed, with sparse fine heterochromatin granules that did not surround the nucleolus (Fig. 1A’). In both the SN and the intermediate (IN) oocytes, nucleoli were enclosed by heterochromatin. However, while the chromatin in SN oocytes was the most condensed, with almost no diffuse chromatin (Fig. 1C’), the chromatin in IN oocytes was less condensed, always with some diffuse chromatin in the nucleoplasm (Fig. 1B’). After OH of prepubertal ovaries at 37°C for 2h or at 39°C for 1 or 2h, the diffuse chromatin in the NSN and IN oocytes condensed into big masses forming the condensed NSN (c-NSN, Fig. 1D’) and condensed IN (c-IN, Fig. 1E’,F’) configurations, respectively (Fig. 1, Table). Some of the NSN oocytes became either IN or SN oocytes after OH at 37°C for 1h. Similar changes in the chromatin configuration were observed in oocytes after OH of adult mouse ovaries, although the proportion of NSN oocytes was very low in the adult ovaries. Our live imaging further confirmed the NSN to c-NSN and IN to c-IN transition (Supplementary Fig. S1). The results suggested that although OH at 37°C for 1h facilitated a normal NSN-to-SN transition, OH at 37°C for 2h or at 39°C for 1 or 2h caused a pseudo (premature) NSN-to-SN transition, generating many oocytes with c-IN configurations.
When oocytes were recovered from fresh ovaries before OH, although none of the oocytes from prepubertal mice formed blastocysts, 40% of those from adult mice did (Table 1), confirming that the culture system used in this study could support maturation of mouse oocytes from ovaries that had not been stimulated with eCG. Compared to those in control oocytes recovered before OH, rates of oocyte maturation, activation and 4-cell embryos decreased significantly after OH at 39°C for 1 or 2h or at 37°C for 2h. After OH at 37°C for 1h, however, percentages of 4-cell embryos increased significantly compared to those in control oocytes, and 10% of the 4-cell embryos developed into blastocysts. The results suggested that although OH for a longer time or at a higher temperature impaired oocyte competence, a short-time OH at body temperature improved oocyte developmental potential.
In all the histone sites observed, levels of acetylation, dimethylation and phosphorylation increased in the NSN, IN and even SN oocytes after OH at 37°C for 1h, but they decreased in SN, c-NSN and c-IN oocytes after OH at 37°C for 2h or at 39°C for 1 or 2h (Table 2, Fig. 2). In the same histone site, the level of histone modification in the c-NSN and c-IN oocytes tended to be lower than that in the NSN and IN oocytes, respectively, indicating that the pseudo NSN-to-SN transition was associated with impaired histone modification. The acetylation level of H4K16 was apparently lower than that of H3K14 and H4K12 in oocytes with various chromatin configurations (Fig. 2). Together with our results shown in Table 1, it is suggested that in all the histone sites examined, the levels of histone modification were positively correlated with the developmental potential of oocytes after different OH treatments.
Both apoptotic percentages and active caspase-3 levels of MGCs were low before OH, but increased significantly with increasing harshness of OH conditions (Fig. 3). Percentages of annexin-positive (apoptotic) oocytes did not differ before OH and after OH at 37°C for 1h, but increased significantly with increasing harshness of OH conditions (Fig. 4). Furthermore, our Hoechst staining showed that the percentage of apoptotic cumulus cells increased significantly after OH at 37°C for 1h compared to that observed before OH (Fig. 3). Taken together, the results suggested that whereas a mild stress induced moderate apoptosis, severe stresses caused heavy apoptosis in mouse oocytes.
Both FasL in MGCs (Fig. 5A) and Fas receptors in oocytes (Fig. 5B) increased significantly with increasing harshness of OH conditions from before OH to OH at 37°C for 1h to 39°C for 1h to 37°C for 2h to 39°C for 2h. Fas receptors in cumulus cells also increased from before OH to OH at 39°C for 1h (Fig. 5D,E). The results suggested that the OH stress induced oocyte apoptosis by activating the Fas system in the ovary.
Annexin-positive percentages and H4K12 acetylation levels in oocytes from freshly collected ovaries (0h) did not differ between wild-type and gld mice (Fig. 6). Following OH at 39°C for 1h, however, whereas the annexin-positive percentages were significantly lower, levels of H4K12 acetylation were significantly higher in gld than in wild-type mice. The results further confirmed that OH stress triggered oocyte apoptosis and impaired epigenetic histone modification by activating the Fas system.
The present results showed that whereas a 1-h OH at body temperature promoted a normal NSN-to-SN transition, OH for a longer time or at a higher temperature caused a pseudo (premature) NSN-to-SN transition, generating the c-IN and c-NSN configurations. The c-IN and c-NSN configurations generated by the pseudo NSN-to-SN transition showed abnormally condensed chromatin masses, which were reminiscent of the pyknotic nuclei observed in apoptotic somatic cells. It is well known that apoptotic cell death in somatic cells is characterized by nuclear pyknosis (chromatin condensation) and DNA fragmentation, among other morphological features20,21. Whereas GV oocytes from young mice with a normal fertility had well-defined NSN and SN configurations, those from old mice with a reduced fertility had chromatin configurations that could not be classified as either NSN or SN29. From the images provided in that report, similarities are obvious between our c-IN and c-NSN configurations and their configurations that could not be classed as either NSN or SN. Furthermore, abnormal chromatin condensation has been observed following chemical treatment of oocytes. For example, when porcine oocytes were treated with roscovitine, the dispersed chromatin disappeared or condensed and the rim of the nucleolus became morphologically incomplete30.
In the present study, whereas OH at 37°C for 1h enhanced histone modification, OH at 37°C for 2h or at 39°C for 1 or 2h impaired histone modification in c-NSN, c-IN, and even in the SN oocytes. Our previous study demonstrated that restraint stress of mice decreased the levels of H3K14 and H4K12 acetylation and of H3K4 and H3K9 dimethylation in SN oocytes. Similar changes in histone acetylation and methylation were observed in oocytes from aged mice. For example, acetylation of H4K12 and H4K16 decreased in GV oocytes from aged mice compared to those in oocytes from young mice31. Whereas GV oocytes from young mice showed dimethylation of H3K4, H3K9, H3K36, H3K79 and H4K20, and trimethylation of H3K9, many GV oocytes from old mice lacked trimethylation of H3K9 and dimethylation of H3K36, H3K79 and H4K2029. Furthermore, feeding mice with mycotoxin decreased oocyte levels of H3K27 trimethylation and H4K20 dimethylation32, and exposure to bisphenol A during follicle culture significantly impaired H3K9 trimethylation33.
Our previous study showed that restraint stress of mice inhibited GV chromatin condensation and hindered the NSN-to-SN transition while increasing the level of H3S10 phosphorylation14. This is different from the present results that OH stress facilitated chromatin condensation and evoked a pseudo NSN-to-SN transition while decreasing the level of H3S10 phosphorylation. It is known that H3S10 phosphorylation plays a dual role during the cell cycle; whereas it maintains relaxed chromatin for active transcription in interphase, it facilitates chromatin condensation during mitosis34. Furthermore, while chronic ethanol consumption increased H3S10 phosphorylation, binge ethanol administration reduced its level of phosphorylation35. Thus, our restraint stress of mice over a 48-h period, which corresponds to a chronic stress, would have hindered the NSN-to-SN transition by increasing the level of H3S10 phosphorylation, whereas OH for 1 or 2h is an acute severer stress, which would have enhanced chromatin condensation by reducing H3S10 phosphorylation in the interphase.
This study demonstrated that whereas OH at 37°C for 1h improved oocyte developmental potential, OH at 37°C for 2h or at 39°C for 1 or 2h decreased oocyte developmental competence. Our further observation indicated that although 1-h OH at 37°C caused only a moderate apoptosis in MGCs and cumulus cells and no apoptosis in oocytes, OH at 37°C for 2h or at 39°C for 1 or 2h induced heavy apoptosis in MGCs and early apoptosis in oocytes. There have been numerous reports that a moderate apoptosis in MGCs or cumulus cells is associated with improved developmental potential of oocytes18,19. Notably, morulae/blastocysts rates of goat oocytes36 and blastocyst hatching rates of bovine oocytes37 were significantly higher in early atretic follicles than in the non- or late atretic follicles. However, the mechanisms for the beneficial effect of the early follicle atresia on oocyte developmental competence are not fully understood. The present results showed that the improved development observed in oocytes with moderately apoptotic MGCs and cumulus cells was associated with accelerated normal NSN-to-SN transition and enhanced histone modification, whereas the impaired development in oocytes with heavy apoptosis was characterized by a premature chromatin condensation (pseudo NSN-to-SN transition) and impaired histone modification. This suggests that early follicle atresia might have improved oocyte competence by accelerating histone modification as well as by promoting a normal NSN-to-SN transition.
The present results showed that while FasL was expressed in MGCs, Fas was expressed in oocytes and cumulus cells, and that both FasL and Fas increased significantly with increasing harshness of the OH conditions. Our observation on percentages of annexin-positive oocytes and levels of H4K12 acetylation indicated that oocytes from gld mice were less harmed by OH than oocytes from wild-type mice. Taken together, the results suggested that OH stress triggered oocyte apoptosis and impaired epigenetic histone modification and oocyte competence by activating the Fas system. Reports on Fas/FasL expression in ovaries are few and those on Fas expression in healthy oocytes are in conflict. In mice, for example, although expression of both Fas and FasL was observed in granulosa cells of both healthy and atretic follicles, Fas was observed only in oocytes of atretic follicles38. In bovine, however, Fas was expressed in normal immature oocytes, whereas FasL was expressed only in cumulus cells26,39. Thus, the present results confirmed Fas expression in healthy mouse oocytes.
In summary, for the first time, the present results showed that OH stress triggered oocyte apoptosis with activation of the Fas/FasL system. Whereas a moderate apoptosis induced by a mild OH stress improved oocyte competence with promoted NSN-to-SN transition and histone modifications, the heavy apoptosis induced by a harsh OH stress impaired oocyte developmental potential with a premature chromatin condensation (pseudo NSN-to-SN transition) and impaired histone modifications. The c-NSN and c-IN configurations generated by the pseudo NSN-to-SN transition could have been mistaken as “SN” configurations in previous reports. Oocytes with the c-NSN and c-IN configurations showed impaired histone modification and reduced developmental potential. Together with our results that the developmental potential of SN oocytes diminished with decreasing levels of histone modifications as OH conditions became harsher, it is suggested that oocyte competence is more closely correlated with histone modification than with chromatin configuration. These data are important for our understanding of the mechanisms by which stress impairs oocyte developmental potential and how the epigenetic factors influence oocyte cytoplasmic maturation.
The experimental procedures were approved by the Animal Care and Use Committee of the Shandong Agricultural University P. R. China (Permit number: SDAUA-2001-0510). The methods were carried out in accordance with the approved guidelines. Unless otherwise specified, all chemicals and reagents used in the present study were purchased from Sigma Chemical Co. (St. Louis, MO, USA).
Mice for most of the experiments in this study are the Kunming strain, which were bred in our laboratory. The gld mice with a germline mutation F273L in FasL in a C57BL/6J genomic background and the wild-type C57BL/6J mice were obtained from the Key Laboratory of Stem Cell Biology, Shanghai Institute for Biological Sciences, China. The mice were kept in a room under a 14L:10D photoperiod, with lights-off at 20:00.
Female mice 18–19 days or 8–12 weeks after birth were sacrificed to collect ovaries without eCG-stimulation. The two ovaries recovered from one mouse were placed in a 1.5-ml microfuge tube containing 1ml pre-warmed M2 medium and stored for 1 or 2h in an incubator with a humidified atmosphere of air and temperature set at either 37°C or 39°C. At the end of OH, the large follicles on the ovary were ruptured in M2 medium to release oocytes. Only oocytes larger than 70μm in diameter and with a homogenous cytoplasm were used.
Oocytes were stripped of their cumulus cells by pipetting in M2 and stained for 5min with 10μg/ml Hoechst 33342 in M2. The stained oocytes were then mounted on a glass slide and observed for GV chromatin configurations under a Leica DMLB fluorescence microscope.
Cumulus-free oocytes were stained in M2 medium containing 50ng/ml Hoechst 33342 for 10min. The oocytes were then cultured at 37°C or 39°C in HCZB medium containing 20ng/ml Hoechst 33342 in an incubator (INUBG2E-ZILCS; Tokai Hit) and observed under a video microscope (DMI6000B; Leica). Time-lapse analysis was performed over a total of 3h period. Phase contrast and fluorescence images of oocytes were taken at 15-min intervals with a charge-coupled device camera (885EM; Andor), and the chromatin was pseudo-colored red.
Because mouse oocytes recovered without eCG priming mature poorly in vitro, oocyte maturation was conducted on cumulus cell monolayer in this study to improve maturation of such oocytes. Briefly, when cumulus cells grew to 80% of confluence, the spent medium in the wells of a 96-well culture plate was replaced with 100μl maturation medium and then equilibrated for 3h in a CO2 incubator. After being washed three times in M2 and once in the maturation medium, the oocytes were placed in the wells (around 35 each well) and culture at 37°C in a humidified atmosphere of 5% CO2 in air. The maturation medium used was TCM-199 (Gibco, Grand Island, NY) supplemented with 10% (v/v) FBS (Gibco), 1μg/ml 17β-estradiol, 24.2mg/ml sodium pyruvate, 0.05IU/ml FSH, 0.05IU/ml LH and 10ng/ml EGF.
At 24h of maturation culture, oocytes were stripped of cumulus cells by pipetting in M2 containing 0.1% hyaluronidase. After being washed twice in M2 and once in the activating medium (Ca2+ -free CZB medium supplemented with 10mM SrCl2 and 5μg/ml cytochalasin B), the oocytes were incubated in the activating medium for 6h at 37°C in a humidified atmosphere with 5% CO2 in air. At the end of activation treatment, the oocytes were examined with a microscope for the evidence of activation. Oocytes were considered activated when each contained one or two well-developed pronuclei. Activated oocytes were cultured for 4 days in regular CZB (30–35 oocytes per 100-μl drop) at 37°C under humidified atmosphere with 5% CO2 in air. Glucose (5.5mM) was added to CZB when embryos developed beyond 3- or 4-cell stages. Embryos were examined at 48h and 96h after activation treatment to record the numbers of 4-cell embryos and blastocysts, respectively.
Procedures used for immunofluorescence were those reported in our previous study14. Briefly, oocytes were stripped of cumulus cells by pipetting in M2. The cumulus-free oocytes and cumulus cells were (1) fixed for 1h with 4% paraformaldehyde; (2) permeabilized (oocytes only) with 0.5% (0.1% for Fas detection) Triton X-100 for 15min (1h for H3S10 phosphorylation); (3) blocked for 1h in D-PBS containing 3% BSA and 0.1% Tween-20; (4) incubated at 4°C overnight with primary antibodies; (5) incubated for 1h with secondary antibodies; (6) stained for 5min with 10μg/ml Hoechst 33342 to visualize the DNA; and (7) mounted on a glass slide and observed with a laser confocal microscope (TCS SP2; Leica Microsystems). When mounting oocytes onto slides, care was taken to ensure that oocytes on different slides were compressed to the same extent and had a similar thickness. Blue diode (405nm) and helium/neon (He/Ne; 543nm) lasers were used to excite Hoechst and CyTM3, respectively. Fluorescence was detected with the following bandpass emission filters: 420–480nm (Hoechst) and 550–570nm (CyTM3), and the captured signals were recorded as blue and red, respectively.
All the oocytes used to observe modifications in the same histone site were processed and observed on the same day. The relative levels of histone acetylation, methylation and phosphorylation and Fas expression were quantified by measuring fluorescence intensities. For each experimental series, all the images were acquired with identical settings. Within the GV of each oocyte, a single plane with maximum amount of chromatin and maximum fluorescence intensity was selected to take photograph for further analysis. Relative intensities were measured on the raw images using the Image-Pro Plus software (Media Cybernetics Inc., Silver Spring, MD) under fixed thresholds across all the slides. Both the fluorescence density and the area of the objects giving the fluorescence were measured and the mean relative intensity of fluorescence was calculated for each oocyte. For each histone modification site, the average relative fluorescence of the NSN oocytes from freshly collected ovaries without holding was set to 1 and that of oocytes from other treatments were expressed relative to this value. The average Fas relative fluorescence of cumulus cells from unpreserved ovaries was set to 1, and those from preserved ovaries were expressed relative to this value.
The primary antibodies included Anti-acetyl-H3 (Lys14) (1:200 dilution, Millipore,06-911), Acetyl Histone H4K12 Polyclonal Antibody (1:1000 dilution, Epigentek, A-4029), Acetyl Histone H4K16 Polyclonal Antibody (1:50 dilution, Epigentek, A-4030), Histone H3K4 Dimethyl Polyclonal Antibody (1:200 dilution, Epigentek, A-4032), Histone H3K9 Dimethyl Polyclonal Antibody (1:100 dilution, Epigentek, A-4035), Anti-phospho-Histone H3 (Ser10) Antibody, clone RR002 (1:100 dilution, Millipore, 05-598), and rabbit polyclonal anti-Fas antibody (dilution 1:100 for oocytes and 1:75 for cumulus cells, Abcam, ab82419). The secondary antibodies used to detect acetylation in H3K14 and H4K12, methylation in H3K4 and H3K9 and Fas were CyTM3-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) (1:800 dilution, Jackson ImmunoRerearsh, 111-165-144), that used to detect acetylation in H4K16 was CyTM3-conjugated Donkey Anti-Goat IgG (H+L) (1:800 dilution, Jackson ImmunoRerearsh, 705-165-147), and that for detecting phosphorylation in H3S10 was CyTM3-conjugated AffiniPure Goat Anti-Mouse IgG (H+L) (1:800 dilution, Jackson ImmunoRerearsh, 115-165-003).
The staining was performed using Annexin V-FITC Apoptosis Detection Kit (Biotool, B32115) according to the manufacturer’s instructions. During the whole process, reagents were kept at 37°C to avoid false positives. Oocytes were placed in 100μl 1×binding buffer containing 5μl Annexin-V/FITC and 5μl propidium iodide, and incubated at room temperature for 15min in the dark. After incubation, 400μl of 1× binding buffer was added, and then the samples were mixed gently and kept on ice or directly mounted on siliconized slides with vaseline bridges and observed under a fluorescent microscope. After treatment with both probes, apoptotic oocytes showed green fluorescence, dead oocytes showed both green and red fluorescence, and healthy oocytes showed little or no fluorescence. Oocytes with more than 20% of the plasma membrane showing green fluorescence were considered annexin-positive. Dead oocytes were not taken into account. Immediately after observation, the oocytes were carefully released from the slides and processed for detection of histone modifications as described above.
The MGCs clumps released into M2 medium at puncture of follicles were collected and pipetted with a thin pipette in M2 medium to separate individual cells. Cumulus cells were prepared by pipetting the cumulus-oocyte complexes with a thin pipette in M2. The MGCs and cumulus cells were then transferred to a 0.5-ml microfuge tube along with the M2 medium and centrifuged for 5min at 200×g. After centrifugation, the MGCs pellets were resuspended in 50μl of M2 medium with 10μg/ml of Hoechst 33342 and stained in the dark for 5min. The stained cells were then centrifuged for 5min at 200×g. After removal of approximately half the supernatant, a 5-μl drop of suspension was smeared on a slide and observed under a Leica DMLB fluorescence microscope. Six to eight fields were randomly examined on each smear, and the percentages of apoptotic cells were calculated from more than 60 cells observed in each field. All images were reviewed by 2 investigators in a double blind manner.
MGCs were placed in a 0.5-ml microfuge tube containing 20μl sample buffer (20mM Hepes, 100mM KCl, 5mM MgCl2, 2mM DTT, 0.3mM phenylmethyl sulfonyl fluoride, 3μg/ml leupetin, 5mM NaF, PH 7.5) and frozen at −80°C until use. For protein extraction, 5μl 5×SDS-PAGE loading buffer was added to each tube, and the tubes were heated at 100°C for 5min. Total proteins were separated on a 12% (for FasL) or 15% (for active caspase-3) polyacrylamide gel by SDS-PAGE and transferred electrophoretically on to PVDF membranes. The membranes were then (1) washed twice in TBST (150mM NaCl, 2mM KCl, 25mM Tris, 0.05% Tween 20, pH 7.4) and blocked for 1h with TBST containing 3% BSA; (2) incubated at 4°C overnight with rabbit polyclonal anti-Fas Ligand antibody (1:1000, ab15285, Abcam Co. Ltd.) or rabbit polyclonal anti-caspase-3 antibody (1:500, ab13847, Abcam Co. Ltd.) and mouse anti-β-tubulin monoclonal antibodies (1:1000, 05-661, Merck Millipore); (3) incubated for 1.5h at 37°C with alkaline phosphatase conjugated goat anti-rabbit IgG (1:1000, cw0111, Kangweishiji Biotechnology Co. Ltd., Beijing, China) and goat anti-mouse IgG (1:1000, cw0110, Kangweishiji Biotechnology Co. Ltd., Beijing, China) antibodies; (4) signals were detected by a BCIP/NBT alkaline phosphatase color development kit (Beyotime Institute of Biotechnology, Haimen City, China). The relative quantities of proteins were determined with Image J software by analyzing the sum density of each protein band image. The quantity of β-tubulin was used for internal control. The density value of each sample was normalized to its β-tubulin density value to get its relative quantity value. The relative quantity values of FasL or active caspase-3 in control ovaries before OH were set as 1 and the other values were expressed relative to this quantity. Each treatment was repeated 3 times with each replicate containing MGCs from 4 ovaries.
There were at least three replicates for each treatment unless otherwise stated. Percentage data were arc sine transformed, and analyzed with ANOVA; a Duncan multiple comparison test was used to locate differences. The software used was Statistics Package for Social Sciences (SPSS 11.5, SPSS Inc. Chicago, IL). Data were expressed as mean±SEM and P<0.05 were considered significant.
How to cite this article: Lin, J. et al. The relationship between apoptosis, chromatin configuration, histone modification and competence of oocytes: A study using the mouse ovary-holding stress model. Sci. Rep. 6, 28347; doi: 10.1038/srep28347 (2016).
This study was supported by grants from the National Basic Research Program of China (Nos 2014CB138503 and 2012CB944403), the China National Natural Science Foundation (No. 31272444) and the Animal breed improvement program of Shandong Province.
Author Contributions J.L., F.C., M.-J.S, J.Zhu, Y.-W.L., L.-Z.P. and J.Zhang. conducted the experiments; J.L. and J.-H.T. analyzed the data; J.-H.T. designed the experiments and wrote the manuscript. All authors reviewed the manuscript.