Mechanisms for post-maturation oocyte aging (PMOA) are not fully understood, and whether autophagy plays any role in PMOA is unknown. To explore the role of autophagy in PMOA, expression of autophagosomes and effects of the autophagy (macro-autophagy) activity on PMOA were observed in mouse oocytes. Oocyte activation rates and active caspase-3 levels increased continuously from 0 to 18 h of in vitro aging. While levels of microtubule-associated protein light chain 3 (LC3)-II increased up to 12 h and decreased thereafter, contents of p62 decreased from 0 to 12 h and then elevated to basal level by 18 h. However, the LC3-II/I ratio remained unchanged following aging in different media or for different times. During in vitro aging up to 12 h, upregulating autophagy with rapamycin or lithium chloride decreased activation susceptibility, cytoplasmic calcium, p62 contents, oxidative stress, caspase-3 activation and cytoplasmic fragmentation while increasing developmental competence, LC3-II contents, LC3-II/I ratio, mitochondrial membrane potential, spindle/chromosome integrity and normal cortical granule distribution. Downregulating autophagy with 3-methyladenine (3-MA) produced opposite effects on all these parameters except cytoplasmic fragmentation. After 12 h of aging culture, however, regulating autophagy with either rapamycin/lithium chloride or 3-MA had no impact on oocyte activation susceptibility. It is concluded that autophagy plays an important role in regulating PMOA. Thus, during the early stage of PMOA, autophagy increases as an adaptive response to prevent further apoptosis, but by the late stage of PMOA, the activation of more caspases blocks the autophagic process leading to severer apoptosis.
If not fertilized or activated in time, mature oocytes undergo a time-dependent process of post-maturation oocyte aging (PMOA)1,2,3,4,5,6. The term PMOA is used instead of post-ovulatory oocyte aging because it covers both in vivo and in vitro matured oocytes. Although it is known that PMOA has marked detrimental effects on embryo development5,7,8,9 and offspring10,11, the mechanisms for PMOA are not fully understood. Studies have shown that PMOA leads to apoptosis. For example, the expression of the antiapoptotic protein BCL2 was gradually reduced during postovulatory oocyte aging12,13,14. Fertilization-like Ca2+ responses induced by injection of sperm cytosolic factor triggered cell death, rather than activation, in aged oocytes15. Furthermore, the aged oocytes exhibited extensive cytoplasmic and DNA fragmentation and activation of protein caspases15,16.
Autophagy is an evolutionarily conserved mechanism by which the cytoplasmic contents are sequestered within autophagosomes and delivered to the lysosome for degradation17. Autophagy is recognized as a cell survival mechanism in starving cells, and it also functions in cell death18. Autophagy has been observed in mouse19 and porcine oocytes20,21,22. Furthermore, in a study to visualize the different routes of ovarian oocyte elimination in rats, Escobar Sánchez et al.23 demonstrated that all phases of the estrous cycle contained dying oocytes that tested positive simultaneously for apoptosis and autophagy markers, suggesting that the proteins involved in both the apoptosis and autophagy processes are present in the same cell at the same time. We thus hypothesize that autophagy may play a role in regulating PMOA. However, there are no reports on the role of autophagy in regulating PMOA.
The objective of this study was to explore the role of autophagy in modulating PMOA by observing expression of autophagosomes in mouse oocytes aging for different times and by determining the effects of autophagic activities on the manifestations of aging oocytes.
Activation rates and autophagosome levels in oocytes aging in different media for different times
To observe the relationship between activation susceptibility and autophagy activity, newly ovulated oocytes collected at 13 h after hCG injections were aged for 12 h in different media before ethanol treatment for activation or western blotting for measurement of LC3 concentrations. While the highest activation rate was observed in oocytes aging in the FasL-rich conditioned medium (FCM), the lowest was in the newly ovulated control oocytes and in oocytes aging in CZB medium supplemented with MG132, with that in oocytes aging in CZB alone in between (Fig. 1a). The highest level of LC3-II was also detected in oocytes aging in FCM, the lowest was in control oocytes, with that in oocytes aging in CZB alone and in CZB + MG132 in between (Fig. 1b). However, the ratio of LC3-II/LC3-I did not change significantly after different treatments (Fig. 1c). Taken together, during the first 12 h of in vitro aging, the autophagosome contents of mouse oocytes increased with increasing activation susceptibility although changes in the rate of autophagic flux were not obvious, suggesting that autophagic activities increased in aging oocytes through both enhanced synthesis and conversion of LC3-I to LC3-II.
The high susceptibility to activating stimulus as an early manifestation of oocyte apoptosis seemed to contradict with the high autophagic activities observed in oocytes aging in FCM for 12 h, as it is generally accepted that autophagy blocks the induction of apoptosis24. Because it has been reported that the apoptosis-associated activation of caspases can switch off the autophagic process24, we hypothesized that the increase in autophagy observed at 12 h of oocyte aging might represent a stress response to prevent further apoptosis, but after that, autophagy would decrease as more caspases were activated with further oocyte aging. To test the hypothesis, freshly ovulated oocytes were aged in FCM medium for different times before ethanol activation or western blot analysis. Although both activation rate (Fig. 1d) and active caspase-3 level (Fig. 1e) increased, the level of LC3-II (Fig. 1f) decreased significantly from 12 h to 18 h of in vitro aging. The LC3-II/LC3-I ratio, however, did not change significantly among oocytes aging for different times (Fig. 1g). The level of p62 decreased significantly from 0 to 12 h of in vitro aging but by 18 h of culture, it increased to the same level as observed in 0 h oocytes (Fig. 1h). This dynamics of p62 protein further confirmed a high autophagic activity at 12 h and a decrease in autophagic activity at 18 h of in vitro aging, as it is known that the expression level of p62 usually correlate inversely with autophagic activity. For example, upon starvation of mouse embryonic fibroblasts and HepG2 cells, p62 was initially degraded by autophagy, but was restored back to basal levels during prolonged starvation25. Furthermore, our immunofluorescence microscopy also indicated that the level of autophagosomes (LC3-II puncta) increased at 12 h but decreased significantly at 18 h of in vitro aging (Fig. 1i, j, k). Taken together, the results showed that oocyte aging is closely correlated with the dynamics of autophagy. Thus, during the early stage of oocyte aging, autophagy increases as an attempt to delay further apoptosis, but by late stages of aging, the activation of more caspases blocks the autophagic process.
Effects of regulating autophagic activities on activation susceptibility, cytoplasmic calcium levels and developmental potential of aging oocytes
To up or down regulate autophagic activities, newly ovulated oocytes were aged for 12 h in FCM containing various concentrations of rapamycin, lithium chloride (LiCl), or 3-methyladenine (3-MA). Control oocytes were aged in FCM with neither rapamycin, LiCl, nor 3-MA. At the end of the aging culture, oocytes were examined for activation rates, cytoplasmic calcium levels, blastocyst rates and LC3 and p62 concentrations. When oocytes were aged with optimal concentrations of rapamycin (10 nM) or LiCl (10 mM), while activation rates (Fig. 2a,b), cytoplasmic calcium levels (Fig. 2d) and p62 contents (Fig. 2h) decreased, blastocyst rates (Fig. 2e), LC3-II levels (Fig. 2f) and LC3-II/I ratio (Fig. 2g) increased significantly, compared to those in control oocytes cultured in FCM alone. When oocytes were aged with 3-MA (5 mM), however, while activation rates (Fig. 2c), cytoplasmic calcium levels (Fig. 2d) and p62 contents (Fig. 2h) increased, blastocyst rates (Fig. 2e), LC3-II levels (Fig. 2f) and LC3-II/I ratio (Fig. 2g) decreased significantly, compared to those in control oocytes. Furthermore, our correlation analysis revealed a significant negative correlation of LC3-II levels with activation rates (r = −0.998) but a positive correlation with the blastocyst rates (r = 0.988) in oocytes aging in different media.
Effects of regulating autophagic activities on oxidative stress and apoptosis of aging oocytes
Freshly ovulated mouse oocytes were aged for 12 h in FCM containing rapamycin, LiCl or 3-MA. Control oocytes were aged in FCM with neither rapamycin, LiCl nor 3-MA. At the end of the aging culture, oocytes were examined for levels of ROS, mitochondrial membrane potential (MMP) and active caspase-3. The results showed that compared to those in control oocytes aging in FCM alone, levels of ROS and active caspase-3 decreased in oocytes aging with rapamycin or LiCl but increased significantly in oocytes aging with 3-MA (Fig. 3). In contrast, while the level of MMP increased in oocytes aging with rapamycin or LiCl, it decreased significantly in oocytes aging with 3-MA, compared to that in control oocytes.
Effects of regulating autophagic activities on spindle/chromosome morphology and cortical granules (CGs) distribution of aging oocytes
Oocytes that had aged for 12 h in FCM alone or in FCM containing 5 mM 3-MA, 10 nM rapamycin or 10 mM LiCl were cultured for 24 h in CZB medium before examination for spindle/chromosome morphology or CGs distribution. Four types of spindle/chromosome morphology were observed: tine pole (Fig. 4a) or barrel-shaped spindles (Fig. 4b) with chromosomes congressed on the metaphase plate, and disintegrated spindles with congressed (Fig. 4c) or scattered chromosomes (Fig. 4d). Compared to those in control oocytes aging in FCM alone, the presence of rapamycin or LiCl in aging medium significantly increased the proportion of oocytes with barrel-shaped spindles and congressed chromosomes while decreasing the oocytes with disintegrated spindles and congressed or scattered chromosomes (Fig. 4e). The presence of 3-MA, however, significantly decreased the number of oocytes with tine pole or barrel-shaped spindles while significantly increasing the percentage of oocytes with disintegrated spindles and scattered chromosomes.
Three patterns of CGs distribution were observed: (a) normal distribution (ND) with all the CGs tidily aligned beneath the plasma membrane except for the CG-free domain above the spindle (Fig. 5a); (b) early migration (EM) of CGs inward and toward the vegetal pole (Fig. 5b); and (c) late migration (LM) of CGs further inward and toward the vegetal pole (Fig. 5c). Over 60% of the oocytes showed EM, ND and LM patterns of CGs distribution following aging in FCM alone, with rapamycin/LiCl or with 3-MA, respectively (Fig. 5d). Taken together, the results suggested that autophagy played an important role in maintaining chromosome/spindle integrity and normal CGs distribution during PMOA.
Effects of regulating autophagic activities on cytoplasmic fragmentation of aging oocytes
Newly ovulated oocytes were aged for 12 h in FCM with or without rapamycin, LiCl or 3-MA, and at the end of the aging culture, the oocytes were incubated in regular CZB medium for different times before observation for cytoplasmic fragmentation. Oocytes with a clear moderately granulate cytoplasm, and an intact first polar body, were considered to be un-fragmented, and oocytes with more than two asymmetric cells were considered to be fragmented26. As expected, supplementation of rapamycin or LiCl to aging culture medium significantly reduced cytoplasmic fragmentation of aging oocytes (Fig. 6). Unexpectedly, however, treatment with 3-MA did not enhance but rather inhibited cytoplasmic fragmentation of aging oocytes. The results suggested that autophagy is involved in the regulation of cytoplasmic fragmentation of aging oocytes but the unexpected effect of 3-MA on cytoplasmic fragmentation of aging oocytes needs further investigations.
Regulating autophagy after 12 h of aging culture had no effects on oocyte activation susceptibility
To further confirm the critical role of autophagy in modulating oocyte aging, effects of regulating autophagy at the time when the autophagosome level had significantly dropped on oocyte activation susceptibility were observed. Following a regular aging culture in FCM alone for 12 h, oocytes were treated with rapamycin, LiCl or 3-MA for 6 or 12 h before observation for ethanol activation rates. The results showed that after in vitro aging for 12 h, treatment with either rapamycin, LiCl or 3-MA for either 6 or 12 h did not affect oocyte activation rates (Fig. 7), suggesting that up or down regulating autophagy at the time when the autophagosome level had significantly declined had no effects on oocyte activation susceptibility.
In this study, oocyte aging in different media for 12 h or in FCM for different times showed that LC3-II contents, but not LC3-II/I ratio, were correlated with oocyte aging parameters, and that the expression level of p62 correlated inversely with LC3-II contents but not with LC3-II/I ratio. It is known that during autophagy induction, LC3-I is lipidated to LC3-II, leading to an increased LC3-II/I ratio. However, while the LC3-II/I ratio is often used as a marker for autophagy in various tissues, there are reports that the LC3-II amount is more representative of autophagy activation than the LC3-II/I ratio is27. The p62 protein has been used as an index of autophagic degradation. Thus, while inhibition of autophagy correlates with increased levels of p62, decreased p62 levels are associated with autophagy activation28. Taken together, the present results suggest that it is the LC3-II amount but not the LC3-II/I ratio that reflects the level of autophagic activity in aging oocytes. Furthermore, the synthesis of p62 in somatic cells depends on its transcriptional upregulation25. Because transcription is inhibited in mature oocytes, the translation of maternal mRNAs stored in the cytoplasm during oogenesis29 may be the primary source for LC3 and p62 expression in aging oocytes.
In this study, while rapamycin and LiCl were used to upregulate, 3-MA was used to down regulate autophagic activities in aging oocytes. LiCl was used to set up an mTOR-independent control for rapamycin, as it has been reported that lithium induced autophagy independently of mTOR by inhibiting inositol monophosphatase30. The results showed that activating autophagy with LiCl produced similar effects as with rapamycin on oocyte aging parameters. This suggests that autophagy in aging oocytes can be activated through alternative pathways other than the mTOR signaling.
The present results suggested that during the early stage of PMOA, autophagy increased as a stress response to prevent further apoptosis; then, the activated autophagy promoted caspase activation; and by the late stage of PMOA, the activation of more caspases in turn blocked the autophagic process itself. In somatic cells, while autophagy may act as a cell survival process by acting as a stress response, delaying caspase activation, and removing damaged organelles, it can also lead to apoptosis by enhancing caspase activation31 or by inhibiting expression of the pro-survival gene Bcl-232. Furthermore, although autophagy blocks the induction of apoptosis in general, apoptosis-associated caspase activation shuts off the autophagic process24. For example, apoptosis induced by the proapoptotic protein Bax reduced autophagy by enhancing caspase-mediated cleavage of Beclin 1 at D14933.
Both the present results and previous studies13,34,35,36,37,38,39 have indicated that PMOA is always associated with increases in oxidative stress, cytoplasmic calcium, activation susceptibility, spindle/chromosome abnormalities and cytoplasmic fragmentation and with impairment of developmental potential, mitochondrial function and CG distribution. The current results showed that upregulating autophagic activities with rapamycin or LiCl inhibited PMOA by correcting these aging parameters, whereas down regulating autophagy with 3-MA accelerated PMOA by aggravating the aging symptoms. It is known that the activation susceptibility of aging oocytes negatively correlates with levels of maturation-promoting factor (MPF) and mitogen-activated protein kinase (MAPK) activities6,40, and that activated protein kinase A maintains both MPF and MAPK in an inactive state41,42. Inhibition of TOR with rapamycin leads to PKA inactivation, and genes involved in almost all steps of autophagy were detected as candidates for PKA negative regulators43. Thus, treatment with rapamycin might have reduced oocyte activation susceptibility by activating MPF and MAPK via inhibiting PKA.
Studies in somatic cells have shown that Ca2+ homeostasis perturbation is the major factor influencing autophagy44. ROS are known to significantly perturb Ca2+ homeostasis through direct effects on intracellular Ca2+ storage45,46 and/or on the Na+/Ca2+ exchanger activity38. Furthermore, increasing ROS levels induces lysosomal Ca2+ release, which enhances autophagy by triggering PPP3/calcineurin-dependent transcription factor EB nuclear translocation47. On the other hand, autophagy is one of the first lines of defense against oxidative stress damage48,49. There are reports that highlight the role of autophagy as a critical protective mechanism against mitochondrial dysfunction. In human cells, accumulation of ROS led to changes in mitochondrial permeability with loss of MMP and disruption of mitochondrial dynamics50. Treatment of rat heart with anti-β1-adrenergic receptor antibodies significantly decreased MMP potential with a marked decrease in autophagy51. Furthermore, autophagy activation with rapamycin significantly protected against mitochondrial dysfunction, whereas genetic inhibition of autophagy induced significant mitochondrial function defects in human chondrocytes52.
In summary, we propose that autophagy plays an important role in regulating PMOA. During the early stage of PMOA, autophagy increases as an adaptive response to prevent further apoptosis, but by the late stage of PMOA, the activation of more caspases blocks the autophagic process leading to severer apoptosis. We believe that our data are important for understanding the mechanisms not only for oocyte aging but also for autophagy and the crosstalk between autophagy and apoptosis.
Materials and methods
All the procedures for animal care and handling were approved by the Animal Care and Use Committee of the Shandong Agricultural University P. R. China (Permit number: SDAUA-2001-001). All the chemicals and reagents used were purchased from Sigma Chemical Company unless otherwise mentioned.
Mice of Kunming breed were raised in a room with 14 h light: 10 h dark cycles, with the dark period starting from 8 pm. Female mice, at the age of 8–10 weeks, were induced to superovulate with 10 IU equine chorionic gonadotropin (eCG, i.p.), followed 48 h later by 10 IU human chorionic gonadotropin (hCG, i.p.). Both eCG and hCG were purchased from Ningbo Hormone Product company limited, China. The superovulated mice were sacrificed 13 h after hCG administration to recover oocytes by breaking the oviductal ampullae. After being washed three times in M2 medium53, the oocytes were denuded of cumulus cells by pipetting in M2 containing 0.1% hyaluronidase and the cumulus-free oocytes were used for experiments.
Preparation of FCM
A FCM was prepared as reported previously33. The cumulus cells released during preparation of cumulus-free oocytes were harvested and cultured for 24 h in regular CZB medium54 containing 200 µM H2O2. The H2O2-treated cumulus cells were then incubated in regular CZB for 48 h, and at the end of the incubation, the conditioned medium was recovered and centrifuged at 3000×g for 5 min to remove cells and debris. The FCM obtained was frozen at −80 °C until use.
Oocyte aging in vitro
Cumulus-free oocytes were cultured for aging in regular CZB medium, FCM or FCM containing various concentrations of MG132, rapamycin, LiCl or 3-MA. To prepare stock solutions, MG132 (5 mM) and rapamycin (10 µM) were dissolved in dimethyl sulfoxide (DMSO), whereas 3-MA (10 mM) and LiCl (10 M) were dissolved in CZB medium and PBS, respectively. All the stock solutions were stored in aliquots at −20 °C and they were diluted to desired concentrations with corresponding aging media immediately before use. The aging culture was performed in wells (about 30 oocytes per well) of a 96-well culture plate containing 100 µl of medium at 37 °C under 5% CO2 in humidified air.
Two activation methods were adopted in this study: ethanol plus 6-dimethylaminopurine (6-DMAP) was used to assess oocyte activation susceptibility, and the SrCl2 was used to evaluate oocyte developmental potential. During ethanol + 6-DMAP treatment, oocytes were first treated with 5% ethanol in M2 medium for 5 min at room temperature, and then cultured in 2 mM 6-DMAP in CZB medium for 6 h at 37.5 °C in a humidified atmosphere containing 5% CO2 in air. For SrCl2 activation, oocytes were incubated for 6 h in Ca2+-free CZB medium supplemented with 10 mM SrCl2 and 5 µg/ml cytochalasin B. At the end of the activation culture, oocytes were observed under a inverted microscope for activation. Oocytes showing one or two pronuclei, or showing two cells each having a nucleolus, were judged as activated.
The Sr2+-activated oocytes were cultured in regular CZB medium (about 30 oocytes per well containing 100 µl medium) at 37.5 °C under a humidified atmosphere with 5% CO2 in air. On day 2 of culture, oocytes were examined for four-cell development, and were transferred to CZB medium containing 5.55 mM glucose for further culture. On day 4.5 of the culture, oocytes were examined for blastocyst formation.
Western blot analysis
Two to three hundreds (for LC3 and p62) or 300–400 (for active caspase-3) cumulus-free oocytes were frozen at −80 °C in a 1.5-ml microfuge tube containing 20 µl sample buffer (20 mM Hepes, 100 mM KCl, 5 mM MgCl2, 2 mM dithiothreitol, 0.3 mM phenylmethyl sulfonyl fluoride, 3 mg/ml leupetin, pH 7.5). To extract protein, 6.67 µl of 5× SDS-PAGE loading buffer was added to each tube and the tubes were heated for 5 min at 100 °C. A SDS-PAGE was performed on a 15% polyacrylamide gel to separate total proteins, and the proteins obtained were transferred onto polyvinylidene fluoride membranes via electrophoresis. The membranes were then (1) washed three times in TBST (50 mM NaCl, 2 mM KCl, 25 mM Tris, 0.05% Tween-20, pH 7.4); (2) blocked for 1–1.5 h at room temperature with TBST containing 3% BSA; (3) incubated overnight at 4 °C with primary antibodies (1: 1000) in 3% BSA-TBST; (4) washed three times (10 min each) in TBST and incubated for 1 h at 37 °C with second antibodies (1: 1000) in 3% BSA-TBST; (5) washed three times in TBST and detected using a BCIP/NBT alkaline phosphatase color development kit (Beyotime Institute of Biotechnology, China). For internal controls, β-tubulin or GAPDH was also assayed. To determine the relative quantities of proteins, the sum density of each protein band image was analyzed using an Image-Pro Plus software. Ratios of target proteins/internal control (β-tubulin or GAPDH) were calculated to represent the quantity values of each target proteins. The primary antibodies used included rabbit anti-LC3 antibody (4108, Cell Signaling, USA), rabbit anti-active caspase-3 polyclonal antibodies (ab13847, Abcam Co. Ltd, Cambridge, MA, USA), rabbit anti-P62 antibody (5114 S, Cell Signaling), mouse anti-β-tubulin monoclonal antibodies (05-661, Merck Millipore, China), and mouse anti-GAPDH monoclonal antibody (CW0100A, CWBIO, China). The secondary antibodies included goat anti-rabbit IgG AP conjugated (cw0111, CWBIO) and goat anti-mouse IgG AP conjugated (cw0110, CWBIO).
Cytoplasmic calcium measurement
To load the Ca2+ probe, cumulus-denuded oocytes were incubated at room temperature for 30 min in HCZB medium containing 1 µM Fura-2 AM and 0.02% pluronic F-27. Drops of HCZB medium were made in a Fluoro dish (FD35-100, World Precision Instruments) and covered with mineral oil. Oocytes were transferred into the HCZB drops and observed with a Leica DMI6000 inverted microscope at 37 °C. A Fura 2 fluorescence module was used for excitation, and a Leica LAS-AF calcium imaging module was used to calculate the F340/380 ratio. The oocytes were monitored for 10 min to record the F340/380 ratio, which represented the concentration of cytoplasmic calcium.
Measurement of intra-oocyte reactive oxygen species (ROS)
Intra-oocyte ROS was quantified by measuring H2O2 levels using 2′,7′-dichlorodihydro-fluorescein diacetate (DCHFDA). Stock solution of DCHFDA (1 mM) was made by dissolving DCHFDA in DMSO and was stored in the dark at −20 °C. Immediately before use, the stock solution was diluted to 10 µM with M2 medium, and cumulus-denuded oocytes were stained with the resultant solution at 37 °C for 10 min. At the end of the staining, the oocytes were thoroughly washed in M2, placed on a slide, and examined under a Leica confocal microscope (TCS SP2) with fluorescence obtained by excitation at 488 nm. All the photographs were taken using fixed microscopic parameters. The fluorescence intensity of each oocyte was analyzed using a Leica software.
Measurement of MMP
An MMP detection (JC-1) kit (Beyotime Biotechnology Research Institute, China) was used to detect MMP. Briefly, cumulus-free oocytes were washed three times with M2 and placed in a drop of 1 ml M2 and 1 ml JC-1 dye working solution. The oocytes were then incubated at 37 °C for 25 min. After being washed three times with a JC-1 staining buffer, the oocytes were observed under a Leica laser scanning confocal microscope. The same oocytes were observed through TRITC channel (red fluorescence) and FITC channel (green fluorescence). The aggregate JC-1 (red fluorescence) was detected at an emission wave length of 590 nm, while the monomeric JC-1 (green fluorescence) was monitored at 529 nm. The ratio of aggregated/ monomeric JC-1 was calculated to quantify changes in MMP, with a decreased red/green JC-1 ratio representing depolarization of the mitochondria.
Immunofluorescence microscopy for detection of LC3, active caspase-3, CGs and tubulin
Procedures were performed at room temperatures unless otherwise specified. Cumulus-free oocytes were washed three times in M2 between treatments. Oocytes were (1) fixed for 30 min with 3.7% paraformaldehyde contained in PBS; (2) treated with 0.5% protease in M2 for 10 seconds to remove zona pellucida; (3) permeabilized at 37.5 °C for 10 min in PBS containing 0.1% Triton X-100; and (4) blocked with 3% BSA in PBS at 37.5 °C for 0.5 h. To detect LC3, blocked oocytes were incubated at 4 °C overnight with rabbit anti-LC3 antibody (1:300, 4108, Cell Signaling) in the antibody diluent, and then, incubated for 1.5 h in the dark with Cy3-conjugated goat-anti-rabbit IgM (1:100, 111-165-144, Jackson ImmunoResearch, USA), and finally, oocytes were incubated for 5 min with 10 µg/ml Hoechst 33342 in M2 to stain chromatin. For active caspase-3 detection, the blocked oocytes were incubated at 37.5 °C for 1 h first with mouse anti-active-caspase-3 (IgM, 1:100, Millipore) in 1% BSA in PBS, and then, with FITC-conjugated donkey-anti-mouse IgM (1:200, 715-095-020, Jackson ImmunoResearch) in 3% BSA in PBS. Then, the oocytes were incubated for 5 min with 10 µg/ml Hoechst 33342 in M2 to stain chromatin. Samples in which the primary antibody was omitted were also processed to serve as negative controls. For tubulin staining, the blocked oocytes were first incubated at 37 °C for 1 h in PBS containing FITC-conjugated anti-α-tubulin monoclonal antibodies (1:50), and then, incubated for 5 min with 10 µg/ml Hoechst 33342 in M2 to stain chromatin. To stain CGs, the blocked oocytes were incubated for 1 h in 100 µg/ml of FITC-labeled lens culinaris agglutinin in M2 followed by incubation for 5 min in M2 containing 10 µg/ml Hoechst 33342 to stain chromatin. The stained oocytes were examined under a Leica confocal microscope, and blue diode (405 nm), argon (488 nm) and helium/neon (He/Ne; 543 nm) lasers were used to excite Hoechst, FITC and Cy3, respectively. Fluorescence was detected with 420-480 nm (Hoechst), 492–520 nm (FITC) and 550–570 nm (Cy3) filters, and the captured signals were recorded as blue, green and red, respectively. To quantify the active caspase-3 expression, the relative fluorescence intensities were measured on the raw images using Image-Pro Plus software (Media Cybernetics Inc., Silver Spring, MD) under fixed thresholds across all slides.
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This study was supported by grants from the National Key R&D Program of China (Nos. 2017YFC1001601 and 2017YFC1001602), the National Basic Research Program of China (Nos. 2014CB138503), the China National Natural Science Foundation (Nos. 31772599 and 31702114), and the Funds of Shandong Double Tops Program (No. SYL2017YSTD12).
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The authors declare that they have no conflict of interest.
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Environmental Science & Technology (2019)
Life Sciences (2019)
Cellular and Molecular Life Sciences (2019)