AMH regulates granulosa cell function via ESR2/ p38-MAPK signaling pathway in sheep

Anti-Müllerian Hormone (AMH), secreted by granulosa cells (GCs) of preantral follicles, regulates early-stage follicle growth by inhibiting the activation of primordial follicles. While GCs facilitate follicle development and ovulation through estrogen and progesterone secretion, the role of AMH in sheep GCs and its impact on follicle development remains unclear. Here, we show that exogenous AMH inhibits primordial follicle development utilizing in vitro culture of fetal sheep ovarian cortex model. Knockdown of AMH in sheep GCs increases cell proliferation, decreases apoptosis, and elevates estradiol (E2) secretion, while overexpression has the opposite effects. RNA-seq analysis suggests that AMH modulates genes involved in cell cycle regulation and MAPK signaling. Notably, AMH downregulates estrogen receptor β (ESR2) expression and suppresses FSH-induced upregulation of aromatase (CYP19A1). These findings demonstrate AMH regulates GCs function through multiple pathways, offering insights into sheep fertility and potential targets to enhance reproductive efficiency.

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Publication Details

Journal
Communications Biology
Published
2025-05-29
DOI
https://doi.org/10.1038/s42003-025-08259-6
Citations
10
Primary Topic
Reproductive Biology and Fertility
Type
article
Field-Weighted Citation Impact
18.79

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article

AMH regulates granulosa cell function via ESR2/ p38-MAPK signaling pathway in sheep

Hui Xu, Wanru Liu, Hua Yang, Chong Zhang et al.
10 citations
Communications Biology
Reproductive Biology and Fertility
18.79
article

AMH regulates granulosa cell function via ESR2/ p38-MAPK signaling pathway in sheep

Hui Xu, Wanru Liu, Hua Yang, Chong Zhang, Feng Wang, Yanli Zhang, Yu‐Dong Cai, Binru Zhao
article en
10 citations

Abstract

Anti-Müllerian Hormone (AMH), secreted by granulosa cells (GCs) of preantral follicles, regulates early-stage follicle growth by inhibiting the activation of primordial follicles. While GCs facilitate follicle development and ovulation through estrogen and progesterone secretion, the role of AMH in sheep GCs and its impact on follicle development remains unclear. Here, we show that exogenous AMH inhibits primordial follicle development utilizing in vitro culture of fetal sheep ovarian cortex model. Knockdown of AMH in sheep GCs increases cell proliferation, decreases apoptosis, and elevates estradiol (E2) secretion, while overexpression has the opposite effects. RNA-seq analysis suggests that AMH modulates genes involved in cell cycle regulation and MAPK signaling. Notably, AMH downregulates estrogen receptor β (ESR2) expression and suppresses FSH-induced upregulation of aromatase (CYP19A1). These findings demonstrate AMH regulates GCs function through multiple pathways, offering insights into sheep fertility and potential targets to enhance reproductive efficiency.

Communications BiologyVol. 8(1)
Nanjing Agricultural University (CN)
National Natural Science Foundation of China, Government of Jiangsu Province, Nanjing Agricultural University, Fundamental Research Funds for the Central Universities
Zero hunger
Openalex Percentile: Top 1%
Reproductive Biology and Fertility
18.79
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