Distinct Luteinization Profiles of Cultured Human Granulosa Cells From Small Antral and Preovulatory Follicles.

IF 5.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Clinical Endocrinology & Metabolism Pub Date : 2025-11-18 DOI:10.1210/clinem/dgaf218
Lea Bejstrup Jensen, Cristina Subiran Adrados, Jane Alrø Bøtkjær, Jesús Cadenas, Sivanandane Sittadjody, Emmanuel Opara, Pernille Landbæk Sørensen, Kirsten Tryde Macklon, Anette Tønnes Pedersen, Stine Gry Kristensen
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Abstract

Context: The transformation of follicular granulosa cells into luteal cells of the corpus luteum remains poorly understood in the human ovary.

Objective: To investigate the luteinization process and steroidogenic differences between granulosa cells from small antral and preovulatory follicles in vitro.

Methods: At the University Hospital of Copenhagen, Denmark, and Wake Forest Institute for Regenerative Medicine, USA, granulosa-lutein cells were obtained from 12 women undergoing IVF treatment, while follicular granulosa cells from unstimulated small antral follicles and corpus luteum were collected from 18 women undergoing ovarian tissue cryopreservation. Cells were cultured for up to 96 hours or 12 days with or without androstenedione or testosterone supplementation and analyzed using RT-qPCR and steroid hormone assays.

Results: In follicular granulosa cells, luteinization markers (CYP11A1, P < .05; STAR, P < .001) increased within 24 to 48 hours, while granulosa markers (HSD17β1, P < .001; CYP19A1, P < .05) decreased within 6 to 12 hours. Luteinizing hormone/choriogonadotropin receptor remained unchanged. By 48 hours, gene expression resembled that of the corpus luteum. In contrast, granulosa-lutein cells exhibited highly luteinized profiles from day 0, with significantly higher progesterone/(17)estradiol ratios. Androgen supplementation and long-term follicle-stimulating hormone exposure did not alter luteinization.

Conclusion: This study uniquely demonstrates that unstimulated follicular granulosa cells undergo a gradual, intrinsic luteinization process, independent of external hormonal triggers. In contrast, granulosa-lutein cells are already highly luteinized upon aspiration. These findings challenge conventional views on luteinization and highlight intrinsic cellular programming as a key driver, offering new insights into ovarian physiology and potential therapeutic targets for reproductive disorders.

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培养的人小窦卵泡和排卵前卵泡颗粒细胞的不同黄体化特征。
背景:卵泡颗粒细胞向黄体黄体细胞的转化在人类卵巢中仍然知之甚少。目的:探讨小卵泡与排卵前卵泡颗粒细胞体外黄体生成过程及体甾质的差异。设计:从12名接受IVF治疗的女性中获得颗粒叶黄素细胞,而从18名接受卵巢组织冷冻保存的女性中收集未受刺激的小腔卵泡和黄体的卵泡颗粒细胞。细胞在添加或不添加雄烯二酮或睾酮的情况下培养96小时或12天,并使用RT-qPCR和类固醇激素检测进行分析。单位:丹麦哥本哈根大学医院和美国维克森林再生医学研究所。结果:在卵泡颗粒细胞中,黄体生成素标记物(CYP11A1, p)。结论:本研究独特地证明,未经刺激的卵泡颗粒细胞经历了一个渐进的、内在的黄体生成素过程,独立于外部激素触发。相反,颗粒叶黄素细胞在抽吸时已经高度黄体化。这些发现挑战了黄体生成素的传统观点,强调了内在细胞编程作为关键驱动因素,为卵巢生理学和生殖疾病的潜在治疗靶点提供了新的见解。
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来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
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