Inhibitory role of activin A during luteinization of follicular and lutein granulosa cells from small antral and preovulatory human follicles

卵泡期 窦卵泡 内分泌学 黄体期 内科学 颗粒细胞 卵泡 化学 人绒毛膜促性腺激素 促黄体激素 卵巢 生物 雌激素 黄体 促性腺激素 激素 卵泡液 男科 细胞培养 促卵泡激素 细胞 月经周期 体外 促排卵素
作者
Lea Bejstrup Jensen,Laura Victoria Højer,Lisette Schönhage,Cristina Subiran Adrados,Jane Alrø Bøtkjær,Tanni Borgbo,Jesús Cadenas,Kirsten Tryde Macklon,Stine Ringholm,Anette Tønnes Pedersen,Stine Gry Kristensen
出处
期刊:Reproductive Biology [Elsevier BV]
卷期号:26 (1): 101169-101169
标识
DOI:10.1016/j.repbio.2025.101169
摘要

Luteinization is a vital process in female reproduction, where granulosa cells differentiate into progesterone-secreting luteal cells. While luteinizing hormone (LH) and human chorionic gonadotropin (hCG) are established promoters of luteinization, the regulatory role of activin A remains incompletely understood. This study aimed to investigate whether activin A can prevent or reverse luteinization in granulosa cells from small antral and preovulatory follicles using an in vitro model. Granulosa cells were collected from women undergoing either IVF treatment or ovarian tissue cryopreservation. Cells were cultured for 48 h with FSH, hCG, or activin A. Hormone secretion (progesterone and estradiol) and content of steroidogenic markers (CYP19A1, STAR, 17βHSD1, 3βHSD2, FSHR, and LHCGR) were analyzed via ELISA, RT-qPCR, and Western blot. RESULTS: demonstrated that activin A suppressed luteinization markers and progesterone production while promoting estrogen synthesis and maintaining granulosa cell features. Conversely, hCG increased luteinization marker expression and progesterone secretion, consistent with its known role in luteal transformation. Notably, granulosa cells from small antral follicles showed a distinct, stage-specific response to activin A compared to those from preovulatory follicles, indicating a temporal regulation of luteinization competence. These findings support a regulatory role for activin A in maintaining granulosa cell identity and delaying luteinization. Understanding the differential responsiveness of granulosa cells across follicular development stages may inform new therapeutic approaches for luteal phase deficiencies and fertility preservation strategies.
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