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Hippo pathway functions as a downstream effector of AKT signaling to regulate the activation of primordial follicles in mice
Author(s) -
Hu LiaoLiao,
Su Tie,
Luo RuiChen,
Zheng YueHui,
Huang Jian,
Zhong ZhiSheng,
Nie Jing,
Zheng LiPing
Publication year - 2019
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.27024
Subject(s) - hippo signaling pathway , yap1 , folliculogenesis , microbiology and biotechnology , protein kinase b , biology , downregulation and upregulation , signal transduction , gene knockdown , effector , pi3k/akt/mtor pathway , medicine , endocrinology , cancer research , transcription factor , cell culture , biochemistry , genetics , embryogenesis , gene , embryo
Clarifying the molecular mechanisms by which primordial follicles are initiated is crucial for the prevention and treatment of female infertility and ovarian dysfunction. The Hippo pathway has been proven to have a spatiotemporal correlation with the size of the primordial follicle pool in mice in our previous work. But the role and underlying mechanisms of the Hippo pathway in primordial follicle activation remain unclear. Here, the localization and expression of the core components were examined in primordial follicles before and after activation. And the effects of the Hippo pathway on primordial follicle activation were determined by genetically manipulating yes‐associated protein 1 ( Yap1 ), the key transcriptional effector. Furthermore, an AKT specific inhibitor (MK2206) was added to determine the interaction between the Hippo pathway and AKT, an important signaling regulator of ovarian function. Results showed that the core components of the Hippo pathway were localized in both primordial and primary follicles and the expression levels of them changed significantly during the initiation of primordial follicles. Yap1 knockdown suppressed primordial follicle activation, while its overexpression led to the opposite trend. MK2206 downregulated the ratio of P‐MST/MST1 and upregulated the ratio of P‐YAP1/YAP1 significantly, whereas Yap1 ‐treatment had no influence on AKT. In addition, YAP1 upregulation partially rescued the suppression of the primordial follicle activation induced by MK2206. Our findings revealed that the Hippo‐YAP1 regulates primordial follicular activation, which is mediated by AKT signaling in mice, thus providing direct and new evidence to highlight the role of Hippo signaling in regulating ovarian follicles development.