4.7 Article

HDAC6 regulates primordial follicle activation through mTOR signaling pathway

期刊

CELL DEATH & DISEASE
卷 12, 期 6, 页码 -

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SPRINGERNATURE
DOI: 10.1038/s41419-021-03842-1

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资金

  1. National Key Research & Developmental Program of China [2018YFC1003700, 2017YFC1001100, 2018YFC1003801]
  2. National Basic Research Program of China [2013CB945501]
  3. Institution of Higher Education Projects of Building First-class Discipline Construction in Ningxia Region (Biology) [NXYLXK2017B05]
  4. National Natural Science Foundation of China [31872792, 31371448, 31571540]
  5. Beijing Natural Science Foundation [5182015, 7182090]
  6. Project of State Key Laboratory of Agrobiotechnology [2015SKLAB4-1, 2016SKLAB-1]

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The primordial follicle pool established during perinatal development is a non-renewable resource that determines female fertility in mammals. HDAC6 functions as a key negative regulator of mTOR in dormant primordial follicles, playing a crucial role in balancing the maintenance and activation of primordial follicles.
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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