HDAC6 regulates primordial follicle activation through mTOR signaling pathway

被引:37
|
作者
Zhang, Tuo [1 ,2 ,3 ]
He, Meina [4 ]
Zhao, Lihua [5 ]
Qin, Shaogang [3 ]
Zhu, Zijian [3 ]
Du, Xinhua [3 ]
Zhou, Bo [3 ]
Yang, Yi [1 ]
Liu, Xinfeng [1 ]
Xia, Guoliang [1 ,3 ]
Chen, Tengxiang [2 ]
Wang, Yuanxi [6 ]
Zhang, Hua [3 ]
Wang, Chao [3 ]
机构
[1] Ningxia Univ, Coll Life Sci, Minist Educ Conservat & Utilizat Special Biol Res, Key Lab, Yinchuan 750021, Ningxia, Peoples R China
[2] Guizhou Med Univ, Sch Basic Med Sci, Guizhou Prov Key Lab Pathogenesis & Drug Res Comm, Dept Physiol, Guiyang 550009, Guizhou, Peoples R China
[3] China Agr Univ, Coll Biol Sci, State Key Lab Agrobiotechnol, Beijing 100193, Peoples R China
[4] Guizhou Med Univ, Sch Basic Med Sci, Dept Biol, Guiyang 550025, Guizhou, Peoples R China
[5] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Pathol & Hepatol, Beijing 100039, Peoples R China
[6] RDFZ Xishan Sch, Beijing 100193, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
PRIMARY OVARIAN INSUFFICIENCY; HISTONE-DEACETYLASE; MOUSE OOCYTES; LIFE-SPAN; CELLS; MAINTENANCE;
D O I
10.1038/s41419-021-03842-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Primordial follicle pool established perinatally is a non-renewable resource which determines the female fecundity in mammals. While the majority of primordial follicles in the primordial follicle pool maintain dormant state, only a few of them are activated into growing follicles in adults in each cycle. Excessive activation of the primordial follicles accelerates follicle pool consumption and leads to premature ovarian failure. Although previous studies including ours have emphasized the importance of keeping the balance between primordial follicle activation and dormancy via molecules within the primordial follicles, such as TGF-beta, E-Cadherin, mTOR, and AKT through different mechanisms, the homeostasis regulatory mechanisms of primordial follicle activation remain unclear. Here, we reported that HDAC6 acts as a key negative regulator of mTOR in dormant primordial follicles. In the cytoplasm of both oocytes and granulosa cells of primordial follicles, HDAC6 expressed strong, however in those activated primordial follicles, its expression level is relatively weaker. Inhibition or knockdown of HDAC6 significantly promoted the activation of limited primordial follicles while the size of follicle pool was not affected profoundly in vitro. Importantly, the expression level of mTOR in the follicle and the activity of PI3K in the oocyte of the follicle were simultaneously up-regulated after inhibiting of HDAC6. The up-regulated mTOR leads to not only the growth and differentiation of primordial follicles granulosa cells (pfGCs) into granulosa cells (GCs), but the increased secretion of KITL in these somatic cells. As a result, inhibition of HDAC6 awaked the dormant primordial follicles of mice in vitro. In conclusion, HDAC6 may play an indispensable role in balancing the maintenance and activation of primordial follicles through mTOR signaling in mice. These findings shed new lights on uncovering the epigenetic factors involved physiology of sustaining female reproduction.
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收藏
页数:12
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