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Updated: Oct 6, 2025

A Tissue Culture Model of Estrogen-producing Primary Bovine Granulosa Cells
Published on: September 6, 2018
Expression and regulation of estrogen receptor 2 and its coregulators in mouse granulosa cells
Chihiro Emori1,2, Takuya Kanke1, Haruka Ito1
1Laboratory of Applied Genetics, Department of Animal Resource Sciences, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8657, Japan.
Abstract:
The cooperative effects of estrogen and oocyte-derived paracrine factors (ODPFs) play critical roles in the normal development of ovarian follicles; however, the mechanism underlying this cooperation has not been well studied. The present study aimed to determine whether ODPFs affect estrogen signaling by regulating the expression of estrogen receptor (ESR) and its coregulators in mouse granulosa cells. Some transcripts encoding ESR coregulators were differentially expressed between cumulus and mural granulosa cells (MGCs). The transcript levels of ESR coregulators, including nuclear receptor corepressor 1 and activator 2, in cumulus cells were significantly suppressed by ODPFs; however, they increased when cumulus cell-oocyte complexes were treated with the transforming growth factor beta receptor I inhibitor, SB431542. Moreover, MGCs exhibited significantly higher ESR2 protein and transcript levels than those in cumulus cells. ODPFs promoted Esr2 expression in cumulus cells but had no effect on that in MGCs. Overall, regulation of the expression of ESR2 and its coregulators in cumulus cells by oocytes seems to be one of the mechanisms underlying estrogen-oocyte cooperation in well-developed antral follicles in mice.
Insights
Oocyte-derived factors regulate estrogen signaling in mouse ovarian granulosa cells. Oocytes control estrogen receptor 2 and coregulator expression, crucial for follicle development.
Area of Science:
- Reproductive Biology
- Endocrinology
- Cell Biology
Background:
- Estrogen and oocyte-derived paracrine factors (ODPFs) are vital for ovarian follicle development.
- The interplay between these factors and their regulatory mechanisms remain incompletely understood.
Purpose of the Study:
- To investigate if ODPFs influence estrogen signaling by modulating estrogen receptor (ESR) and coregulator expression in mouse granulosa cells.
- To elucidate the role of ODPFs in the cooperative signaling between oocytes and granulosa cells.
Main Methods:
- Differential expression analysis of ESR coregulator transcripts in cumulus versus mural granulosa cells (MGCs).
- Treatment of cumulus-oocyte complexes with ODPFs and SB431542 (transforming growth factor beta receptor I inhibitor).
- Quantification of ESR2 protein and transcript levels in different granulosa cell types.
Main Results:
- ODPFs significantly suppressed specific ESR coregulator transcripts in cumulus cells, an effect reversed by SB431542.
- Mural granulosa cells displayed higher ESR2 protein and transcript levels compared to cumulus cells.
- ODPFs enhanced Esr2 expression in cumulus cells but not in MGCs.
Conclusions:
- Oocyte-derived factors regulate ESR2 and its coregulator expression in cumulus cells.
- This regulation represents a key mechanism in estrogen-oocyte cooperation during antral follicle development in mice.
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