Xu Jiao, Cao Xiu-Ping, Tang Zi-Juan, Huang Jian, Zheng Yue-Hui, Li Jia
The First Clinical Medical School, College of Medicine, Nanchang University, Nanchang 330006, China.
School of Basic Medical Sciences, College of Medicine, Nanchang University, Nanchang 330006, China.
Sheng Li Xue Bao. 2019 Jun 25;71(3):405-414.
The present study was aimed to investigate the expression relationship of Hippo signaling molecules and ovarian germline stem cell (OGSC) markers in the development schedule of OGSCs during ovarian aging in women and mice. The ovaries of 2-month-old mature (normal control) and 12-month-old (physiological ovarian aging) KM mice were sampled, and the ovarian cortex samples of young (postpuberty to 35 years old), middle age (36-50 years old) and menopausal period (51-60 years old) women were obtained with consent. The mice model of pathological ovarian aging was established by intraperitoneal injection of cyclophosphamide/busulfan (CY/BUS). HE staining was used to detect the changes of follicles at different stages, and the localization and expression changes of Hippo signaling molecules and OGSCs related factors (MVH/OCT4) were detected by immunohistochemistry and immunofluorescence staining. Western blot was used to detect the protein expression levels of the major molecules in the Hippo signaling pathway and OGSCs related factors. The results showed that there were not any normal follicles, but a few atresia follicles in the ovaries from physiological and pathological ovarian aging mice. Compared with the normal control mice, both the physiological and pathological ovarian aging mice showed decreased protein expression levels of the main Hippo signaling molecules (pYAP1) and MVH/OCT4; Whereas only the pathological ovarian aging mice showed increased ratio of pYAP1/YAP1. In comparison with the young women, the middle age and menopausal women showed looser structure of ovarian surface epithelium (OSE) and less ovarian cortical cells. The protein expression level of LATS2 in the OSE was the highest in young women, MST1 expression was the lowest in the menopausal period women, and the expression levels of YAP1 and pYAP1 were the highest in middle age women. Compared with the young women, the middle age and menopausal period women exhibited significantly decreased ratio of OSE pYAP1/YAP1, whereas there was no significant difference between them. The expression level of MVH protein in OSE from the young women was significantly higher than those of the middle age and menopausal period women. These results indicate that there is an expression relationship between the main molecules of Hippo signaling pathway and OGSCs related factors, which suggests that Hippo signaling pathway may regulate the expression levels of OGSCs related factors, thus participating in the process of physiological and pathological degeneration of ovarian.
本研究旨在探讨河马信号分子与卵巢生殖系干细胞(OGSC)标志物在女性和小鼠卵巢衰老过程中OGSCs发育进程中的表达关系。采集2月龄成熟(正常对照)和12月龄(生理性卵巢衰老)KM小鼠的卵巢,征得同意后获取青年(青春期后至35岁)、中年(36 - 50岁)和围绝经期(51 - 60岁)女性的卵巢皮质样本。通过腹腔注射环磷酰胺/白消安(CY/BUS)建立病理性卵巢衰老小鼠模型。采用HE染色检测不同阶段卵泡的变化,通过免疫组织化学和免疫荧光染色检测河马信号分子和OGSCs相关因子(MVH/OCT4)的定位及表达变化。利用蛋白质免疫印迹法检测河马信号通路主要分子及OGSCs相关因子的蛋白表达水平。结果显示,生理性和病理性卵巢衰老小鼠的卵巢中均无正常卵泡,仅有少数闭锁卵泡。与正常对照小鼠相比,生理性和病理性卵巢衰老小鼠的主要河马信号分子(pYAP1)及MVH/OCT4的蛋白表达水平均降低;而仅病理性卵巢衰老小鼠的pYAP1/YAP1比值升高。与青年女性相比,中年和围绝经期女性的卵巢表面上皮(OSE)结构更松散,卵巢皮质细胞更少。OSE中LATS2蛋白表达水平在青年女性中最高,MST1表达在围绝经期女性中最低,YAP1和pYAP1表达水平在中年女性中最高。与青年女性相比,中年和围绝经期女性的OSE pYAP1/YAP1比值显著降低,而二者之间无显著差异。青年女性OSE中MVH蛋白表达水平显著高于中年和围绝经期女性。这些结果表明,河马信号通路主要分子与OGSCs相关因子之间存在表达关系,提示河马信号通路可能调节OGSCs相关因子的表达水平,从而参与卵巢生理性和病理性退变过程。