Macrophage colony-stimulating factor (M-CSF) is an intermediate in the process of luteinizing hormone-induced decrease in natriuretic peptide receptor 2 (NPR2) and resumption of oocyte meiosis
Luteinizing hormone (LH) regulation of the ligand, natriuretic peptide precursor type C, and its receptor, natriuretic peptide receptor 2 (NPR2), is critical for oocyte maturation; however, the mechanism is not fully understood. Macrophage colony-stimulating factor (M-CSF) has recently been shown to be involved in oocyte maturation and ovulation. In the present study we determined whether or not M-CSF plays a role in the intermediate signal that mediates LH regulation of NPR2 in resumption of oocyte meiosis.
Immature female C57BL/6 mice were injected i.p. with 5 IU of equine chorionic gonadotropin (eCG) to stimulate follicle development. After 44–48 h, the eCG-stimulated mice were injected i.p. with an ovulatory dose of 5 IU of human chorionic gonadotropin (hCG). The ovaries were excised at selected times. Pre-ovulatory follicles (POFs) and cumulus-oocyte complexes were cultured in different media. Immunohistochemical and quantitative real-time PCR analyses were used to assess the expression of M-CSF, M-CSF receptor (M-CSF-R), and NPR2. The presence of germinal vesicle breakdown (GVBD) was examined under a stereomicroscope to morphologically evaluate resumption of oocyte meiosis.
NPR2 was mainly expressed in cumulus cells of pre-ovulatory follicles, while M-CSF and M-CSF-R were expressed in both mural granulosa and cumulus cells. The levels of M-CSF/M-CSF-R and NPR2 decreased within 4 h after treatment of hCG. M-CSF not only reduced the expression of NPR2 mRNA via its receptor (M-CSF-R), but also increased the proportion of GVBD in oocytes.
M-CSF serves as an intermediate signal, thus inducing a vital decrease in the NPR2 levels in cumulus cells, and regulates the process of LH-induced resumption of meiosis.
KeywordsLuteinizing hormone Macrophage colony-stimulating factor Meiosis resumption Natriuretic peptide receptor 2 Oocyte
cyclic adenosine 3′,5′-monophosphate
cyclic guanosine 3′,5′-monophosphate
Equine chorionic gonadotropin
Epidermal growth factor receptor
Fetal bovine serum
Germinal vesicle breakdown
Human chorionic gonadotropin
Integrated optical density
Macrophage colony-stimulating factor
Minimum essential media
Natriuretic peptide precursor type C
Natriuretic peptide receptor 2
Oocytes resume meiosis when the luteinizing hormone (LH) surge causes dramatic changes in pre-ovulatory follicles (POFs) [16, 17]. It has been shown that LH causes a spectacular decrease in NPPC in the follicles of a wide variety of mammalian species, including mice, rats, pigs, and humans [4, 5, 13, 18, 19]. Decreased NPPC in turn reduces the amount of NPR2 and cGMP, and meiosis resumes in oocytes [4, 5]. Recently, when the kinetic curve of cytokines was further studied, NPPC was not shown to be decreased until 2 h after the LH surge, whereas the decrease in cGMP was first detected at 15–20 min . NPR2 also undergoes a rapid decrease in activity within 10 min after LH exposure, when the NPPC concentration is constant [20, 21]. This phenomenon (that the receptor is motivated before ligand activation) gave rise to the hypothesis that multiple pathways mediate LH regulation of NPR2 and downstream cGMP signaling in the ovarian follicle . These multiple pathways include the phosphoprotein phosphatase signaling pathway , which has recently been associated with ovulation process. Multiple pathways are known to include the epidermal growth factor receptor (EGFR) signaling pathway [21, 22, 23, 24, 25, 26], but recent findings have shown new relationships. The exact number of these multiple pathways is unknown.
Macrophage colony-stimulating factor (M-CSF), a hemopoietic growth factor with a classic function of controlling the proliferation and differentiation of macrophages, has recently been shown to be involved in oocyte maturation and ovulation [27, 28, 29, 30]. We have previously reported that M-CSF is implicated in follicular GC function , and M-CSF can modulate the generation of NPPC, which may regulate ovulation triggered by LH . In the present study we determined whether or not M-CSF is included in the aforementioned “multiple pathways” that mediate LH regulation of NPR2 in ovarian follicles.
Animals and hormone treatments
Immature (22–25 days old) female C57BL/6 mice (Zhejiang Academy of Medical Sciences, Hangzhou, China) were injected i.p. with 5 IU of equine chorionic gonadotropin (eCG) to stimulate follicle development. After 44–48 h, the eCG-stimulated mice were injected i.p. with an ovulatory dose of human chorionic gonadotropin (hCG; 5 IU). The ovaries were excised at selected times after injection and processed for immunohistochemical analysis and quantitative real-time PCR. For cell culture of POFs and cumulus-oocyte complexes (COCs), the eCG-stimulated mice were euthanized and the ovaries were excised without hCG injection. All chemicals were purchased from Sigma-Aldrich (St. Louis, MO, USA) unless otherwise stated. All animal procedures were approved by the guidelines of the Nanjing Medical University Administrative Panel on Laboratory Animal Care.
Culture of POFs
The POFs were dissected stereomicroscopically from the ovaries of eCG-stimulated mice, as previously described [32, 33]. The POFs were placed in minimum essential media (MEM)-α supplemented with 100 mg/ml of fetal bovine serum (FBS), 100 U/ml of penicillin G, and 100 μg/ml of streptomycin sulfate. After equilibration, follicles (10–15 per group) were cultured at 37 °C in an atmosphere of 5% O2, 5% CO2, and 90% N2 for the indicated time in the presence or absence of hCG (5 IU/ml). At the end of the culture period, follicles were collected for quantitative RT-PCR analysis to measure hCG regulation of NPR2 transcript levels.
Culture of COCs
COCs were obtained by puncturing the POFs in the ovaries from eCG-stimulated mice. After isolation, COCs were washed in the medium and cultured for 2 h. The culture medium was MEM-α supplemented with 100 mg/ml of FBS, 100 U/ml of penicillin G, and 100 μg/ml of streptomycin sulfate with or without 30 nM NPPC. At least 10 COCs per treatment group were cultured. Cultures were maintained under a controlled atmosphere of 5% O2, 5% CO2, and 90% N2 at 37 °C. After culture, COCs were collected for quantitative RT-PCR to calculate the NPR2 transcript levels. The presence of germinal vesicle breakdown (GVBD) was examined under a stereomicroscope.
RNA isolation, reverse transcription, and quantitative real-time PCR
Primer sequences, forward (F) or reverse (R), used for quantitative RT-PCR
F or R
The excised ovaries were fixed in 10% formalin. After dehydration, the fixed ovaries were embedded in paraplast, then sectioned at 5-μm intervals onto Superfrost Plus microscope slides. For immunohistochemical staining, sections of ovaries were deparaffinized and rehydrated, treated with 3% H2O2 for 20 min to inactivate intrinsic peroxidase activity, and incubated with ethylene dinitrilo tetraacetic acid buffer for 10 min for antigen retrieval. Washes were carried out with automation phosphate buffer. Sections were incubated for 2 h at 4 °C with rabbit anti-mouse antibody diluted 1:200 in buffer containing 5% bovine serum albumin. Sections were next incubated with horseradish peroxidase-labeled goat anti-rabbit antibody for 50 min at room temperature. Staining was achieved using diaminobenzidine chromogen. The staining reactions were stopped with distilled water, and sections were dehydrated and mounted with neutral balsam.
Image analysis of densitometry
Slides were examined under a microscope with a 200 × objective. The obtained images were captured and examined by Image Pro Plus 6.0 software (Media Cybernetics, Inc., Washington, USA). The integrated optical density (IOD) was calibrated, and the area of interest was set. The mean optical density was defined as the IOD divided by the total area examined.
Statistical analyses were carried out using SPSS software (version 16.0: SPSS, Inc., Chicago, IL, USA). Data are presented as the mean ± SEM. Differences between experimental and control groups were analyzed by ANOVA test. Statistical significance was set at P value of less than 0.05.
Localization of M-CSF, M-CSF-R, and NPR2 in POFs
Changes in expression of M-CSF, M-CSF-R, and NPR2 in the ovaries of mice injected with gonadotropin
Kinetic curve of NPR2 mRNA levels controlled by hCG in vitro
M-CSF/M-CSF-R signaling decreases the level of NPR2 mRNA in cumulus cells and contributes to resumption of meiosis in oocytes
In the present study, we focused on the effect of M-CSF in the regulation of oocyte meiosis, and identified some crucial roles, including: (a) NPR2 was mainly expressed in cumulus cells of POFs, while M-CSF and M-CSF-R were expressed in both mural GCs and cumulus cells; (b) the levels of M-CSF/M-CSF-R and NPR2 decreased within 4 h after hCG treatment; and (c) M-CSF not only reduced the expression of NPR2 mRNA via its receptor (M-CSF-R), but also increased the proportion of GVBD of oocytes, which indicates that M-CSF is an intermediate signal, inducing a vital decrease in NPR2 levels in cumulus cells, and regulates the process of LH-induced resumption of meiosis.
M-CSF extensively participates in the processes of ovulation [27, 29]. Female mice lacking the coding region for the M-CSF gene (M-CSF deficient) have remarkably lower ovulation rates compared to the wild-type counterparts. Indeed, administration of M-CSF from birth to reinstate circulating M-CSF levels could reverse these defects . In humans, high serum concentrations of M-CSF were related to successful oocyte retrieval during in-vitro fertilization and embryo transfer cycles . LH surge triggers dramatic changes in cytokines during ovulation . Although the changes in M-CSF and M-CSF-R 24 h after a LH surge are clear , the alteration in M-CSF/M-CSF-R within a short period of time (4 h) following the LH surge is unknown. Therefore, we studied the changes in M-CSF/M-CSF-R expression in the ovaries of mice injected with gonadotropin. The data from our study showed that M-CSF/M-CSF-R, expressed in both mural GCs and cumulus cells, was gradually decreased within 4 h after hCG treatment. We hypothesized that this change is related to estradiol (E2). Reportedly, the expression of M-CSF was enhanced by E2 in luteinized GCs in a dose-dependent manner in vitro . E2 maintains cumulus cell expression of NPR2 and inhibits the resumption of meiosis in mouse oocytes in vitro , and the level decreased during ovulation. Thus, decreased E2 has a certain role to the resumption of oocyte meiosis and ovulation. Therefore, the decreased level of M-CSF after hCG treatment may be due to the decreased levels of E2. Although the hypothesis is theoretically feasible, it is still necessary to further investigate whether or not a decrease in M-CSF during ovulation is related to a decrease in the E2 level.
Recent studies have revealed that cGMP stimulated by NPR2 from cumulus cells diffuses into oocytes via gap junctions and controls cAMP concentration through inhibition of PDE3A activity, indicating that higher NPR2 levels in cumulus cells is responsible for oocyte meiotic arrest by maintaining high cAMP levels in oocytes [1, 4, 5, 6, 7]. Our results showed that NPR2 is primarily expressed in cumulus cells surrounding oocytes, which is consistent with the literature. The results presented herein support the thought that control of NPR2, which is expressed in cumulus cells, is essential for maintaining meiotic arrest in pre-ovulatory oocytes [4, 13]. LH reduces the activity of NPR2 during ovulation, and promotes resumption of meiosis in oocytes . In particular, our findings demonstrated that NPR2 is also expressed in peri-antral mural GCs (GCs situated on the antral side), which substantiates the viewpoint that some mGCs are activated by NPPC in an autocrine process to raise cGMP levels [24, 34]. NPR2 was down-regulated following a specific time curve after hCG injection. The kinetic curve of NPR2 after hCG treatment in our study was similar to that reported in the literature , but there were some differences. In our research, NPR2 expression peaked 1 h after hCG treatment, and an obvious reduction of approximately 85% in expression was detected at 4 h in vivo. The rise in NPR2 expression within 2 h after LH treatment was different from that reported in the literature, likely due to the long half-life (40 ~ 120 h) of eCG administered 48 h before hCG injection to stimulate follicle development [22, 24]. The eCG promoted the up-regulation of NPR2 during follicle growth . To clarify the NPR2 expression change within 2 h after LH treatment, cultured POFs were used to examine the kinetic curve of NPR2 mRNA levels controlled by hCG in vitro. The data from our study were consistent with the literature . We did not observe a significant increase in expression of NPR2 in hCG-containing media in vitro, possibly because in vitro culture eliminated the residual effect of eCG. To further declare the effect of M-CSF/M-CSF-R signaling on NPR2 mRNA expression and oocyte maturation, COCs isolated from POFs were cultured. The results showed that the M-CSF/M-CSF-R signaling reduced levels of NPR2 mRNA in cumulus cells and promoted resumption of oocyte meiosis. Then, we added GW2580 to restrict the effect of M-CSF signaling in vitro. The results showed that the effect of M-CSF at 4 h was partially abolished.
We conclude that M-CSF is an intermediate signal, inducing a vital decrease in NPR2 levels in cumulus cells, and regulates the process of LH-induced resumption of meiosis. Although further research is needed, our findings bring forth powerful evidence to interpret “multiple pathways” that mediate LH regulation of NPR2 in the process of resuming oocyte meiosis.
We acknowledge core support provided by the National Natural Science Foundation of China (grant no. 31470078).
The study was funded by core support provided by the National Natural Science Foundation of China (grant no. 31470078).
Availability of data and materials
All data generated or analyzed during this study are included in this published article. The datasets used during the current study are available from the corresponding author on reasonable request.
YF, GZ and WZ did experiments, performing data analysis and assisted with manuscript preparation. WS, CL and XF cooperated with sample collection and preparation. XF and ZZ edited the manuscript. ZZ designed study and prepared manuscript. All authors read and approved the final manuscript.
All animal procedures were approved by the guidelines of the Nanjing Medical University Administrative Panel on Laboratory Animal Care. The study does not include any human samples.
Consent for publication
The authors declare that they have no competing interests.
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