Follicle stimulating hormone controls granulosa cell glutamine synthesis to regulate ovulation.
Kai-Hui ZhangFei-Fei ZhangZhi-Ling ZhangKe-Fei FangWen-Xing SunNa KongMin WuHai-Ou LiuYan LiuZhi LiQing-Qing CaiYang WangQuan-Wei WeiPeng-Cheng LinYan LinWei XuCong-Jian XuYi-Yuan YuanShi-Min ZhaoPublished in: Protein & cell (2024)
Polycystic ovary syndrome (PCOS) is the leading cause of anovulatory infertility. Inadequate understanding of the ovulation drivers hinders PCOS intervention. Herein, we report that follicle stimulating hormone (FSH) controls follicular fluid (FF) glutamine levels to determine ovulation. Murine ovulation starts from FF-exposing granulosa cell (GC) apoptosis. FF glutamine, which decreases in pre-ovulation porcine FF, elevates in PCOS patients FF. High-glutamine chow to elevate FF glutamine inhibits mouse GC apoptosis and induces hormonal, metabolic, and morphologic PCOS traits. Mechanistically, follicle-development-driving FSH promotes GC glutamine synthesis to elevate FF glutamine, which maintain follicle wall integrity by inhibiting GC apoptosis through inactivating ASK1-JNK apoptotic pathway. FSH and glutamine inhibit the rapture of cultured murine follicles. Glutamine removal or ASK1-JNK pathway activation with metformin or AT-101 reversed PCOS traits in PCOS models that are induced with either glutamine or EsR1-KO. These suggest that glutamine, FSH, and ASK1-JNK pathway are targetable to alleviate PCOS.
Keyphrases
- polycystic ovary syndrome
- insulin resistance
- cell death
- signaling pathway
- oxidative stress
- adipose tissue
- single cell
- end stage renal disease
- metabolic syndrome
- cell cycle arrest
- stem cells
- ejection fraction
- chronic kidney disease
- bone marrow
- newly diagnosed
- prognostic factors
- genome wide
- skeletal muscle
- liquid chromatography