A Dynamic Shift in Estrogen Receptor Expression During Granulosa Cell Differentiation in the Ovary.

IF 3.8 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM Endocrinology Pub Date : 2025-01-06 DOI:10.1210/endocr/bqaf006
Chan Jin Park, Ji-Eun Oh, PoChing Lin, Sherry Zhou, Mary Bunnell, Emmanuel Bikorimana, Michael J Spinella, Hyunjung Jade Lim, CheMyong J Ko
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Abstract

This study uncovers a dynamic shift in estrogen receptor expression during granulosa cell (GC) differentiation in the ovary, highlighting a transition from estrogen receptor alpha (ESR1) to estrogen receptor beta (ESR2). Using a transgenic mouse model with Esr1-iCre-mediated Esr2 deletion, we demonstrate that ESR2 expression is absent in GCs derived from ESR1-expressing ovarian surface epithelium (OSE) cells. Single-cell analysis of the OSE-GC lineage reveals a developmental trajectory from Esr1-expressing OSE cells to Foxl2-expressing pre-GCs, culminating in GCs exclusively expressing Esr2. Transcriptome analyses identified vasculature-derived TGFβ1 ligands as key regulators of this transition. Supporting this, TGFβ1 treatment of cultured embryonic ovaries reduced Esr1 expression while promoting Esr2 expression. This study underscores the capability of GCs to switch from ESR1 to ESR2 expression as a fundamental aspect of normal differentiation.

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卵巢颗粒细胞分化过程中雌激素受体表达的动态变化。
本研究揭示了卵巢颗粒细胞(GC)分化过程中雌激素受体表达的动态变化,强调了从雌激素受体α (ESR1)到雌激素受体β (ESR2)的转变。通过esr1 - icre介导的Esr2缺失转基因小鼠模型,我们发现Esr2在表达esr1的卵巢表面上皮(OSE)细胞衍生的GCs中缺失。对OSE- gc谱系的单细胞分析揭示了从表达esr1的OSE细胞到表达foxl2的前gc细胞的发育轨迹,最终形成完全表达Esr2的gc细胞。转录组分析发现血管源性TGFβ1配体是这一转变的关键调节因子。tgf - β1处理培养的胚胎卵巢降低了Esr1的表达,同时促进了Esr2的表达。这项研究强调了GCs从ESR1到ESR2表达转换的能力,这是正常分化的一个基本方面。
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来源期刊
Endocrinology
Endocrinology 医学-内分泌学与代谢
CiteScore
8.10
自引率
4.20%
发文量
195
审稿时长
2-3 weeks
期刊介绍: The mission of Endocrinology is to be the authoritative source of emerging hormone science and to disseminate that new knowledge to scientists, clinicians, and the public in a way that will enable "hormone science to health." Endocrinology welcomes the submission of original research investigating endocrine systems and diseases at all levels of biological organization, incorporating molecular mechanistic studies, such as hormone-receptor interactions, in all areas of endocrinology, as well as cross-disciplinary and integrative studies. The editors of Endocrinology encourage the submission of research in emerging areas not traditionally recognized as endocrinology or metabolism in addition to the following traditionally recognized fields: Adrenal; Bone Health and Osteoporosis; Cardiovascular Endocrinology; Diabetes; Endocrine-Disrupting Chemicals; Endocrine Neoplasia and Cancer; Growth; Neuroendocrinology; Nuclear Receptors and Their Ligands; Obesity; Reproductive Endocrinology; Signaling Pathways; and Thyroid.
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