Zhao Jinghua, Sun Yuhan, Liswaniso Simushi, Wu Hengsong, Sun Xue, Yan Chunchi, Qin Ning, Xu Rifu
College of Animal Science and Technology, Jilin Agricultural University, Changchun 130118, China.
School of Life Sciences, Changchun Normal University, Changchun 130032, China.
Genes (Basel). 2025 Apr 27;16(5):500. doi: 10.3390/genes16050500.
Follicle stimulating hormone (FSH) is key regulator for follicular development, differentiation, and maturation, and the effects involve various intra follicular factors, such as members of the forkhead box O (FOXO) subfamily. However, the specific role and mechanism of FOXO3 and FOXO4 in growth and development of hen follicles by affecting granulosa cell (GC) division and FSH response function are still unclear.
This study selected GCs from 6-8 mm chicken follicles, and immunofluorescence and Western blot methods were used to detect FSH-induced FOXO3/4 phosphorylation and nuclear exclusion. Quantitative real-time PCR and flow cytometry were used to investigate the regulatory effects of FSH-induced FOXO3/4 phosphorylation and nuclear exclusion on follicular GC proliferation, differentiation, and apoptosis.
This study found that the level of p-FOXO3/4 protein significantly increased in cells treated with FSH for 12 h, while the expression level of non-phosphorylated FOXO3/4 significantly decreased. After co-treatment with 10 ng/mL Leptomycin B (LMB), FOXO3/4 phosphorylation was effectively prevented. The immunofluorescence results showed that FOXO3 and FOXO4 were originally distributed in the GC nucleus and cytoplasm, whereas they were almost accumulated in cytoplasm when treated with FSH for 12 h. Conversely, FOXO3/4 nuclear translocation was blocked by LMB. Moreover, RT-qPCR and flow cytometry results showed that FSH treatment significantly increased proliferation and differentiation of cells but significantly reduced GCs apoptosis. However, LMB also eliminated these stimulating or inhibitory effects on cell proliferation.
These findings provide new evidence that FSH-induced FOXO3/4 nuclear exclusion promotes GCs proliferation and reduces GCs apoptosis during hen follicular development.
促卵泡生成素(FSH)是卵泡发育、分化和成熟的关键调节因子,其作用涉及多种卵泡内因子,如叉头框O(FOXO)亚家族成员。然而,FOXO3和FOXO4通过影响颗粒细胞(GC)分裂和FSH反应功能在母鸡卵泡生长发育中的具体作用及机制仍不清楚。
本研究选取6 - 8毫米鸡卵泡的颗粒细胞,采用免疫荧光和蛋白质免疫印迹法检测FSH诱导的FOXO3/4磷酸化及核输出。运用实时定量PCR和流式细胞术研究FSH诱导的FOXO3/4磷酸化及核输出对卵泡颗粒细胞增殖、分化和凋亡的调节作用。
本研究发现,用FSH处理12小时的细胞中,p - FOXO3/4蛋白水平显著升高,而未磷酸化的FOXO3/4表达水平显著降低。与10纳克/毫升的雷帕霉素B(LMB)共同处理后,FOXO3/4磷酸化得到有效抑制。免疫荧光结果显示,FOXO3和FOXO4最初分布在颗粒细胞核和细胞质中,而用FSH处理12小时后它们几乎都聚集在细胞质中。相反,LMB阻止了FOXO3/4的核转位。此外,实时定量PCR和流式细胞术结果表明,FSH处理显著增加了细胞的增殖和分化,但显著降低了颗粒细胞的凋亡。然而,LMB也消除了这些对细胞增殖的刺激或抑制作用。
这些发现提供了新的证据,表明FSH诱导的FOXO3/4核输出在母鸡卵泡发育过程中促进颗粒细胞增殖并减少颗粒细胞凋亡。