Estrogen receptor α and β expression in theca and granulosa cells from women with polycystic ovary syndrome

87Citations
Citations of this article
51Readers
Mendeley users who have this article in their library.

Abstract

A defining characteristic of dominant follicles is high estradiol concentrations. Abnormal expression of estrogen receptors (ERs) could contribute to poor follicular development and ovulatory failure in polycystic ovary syndrome (PCOS). The aim of this study was to determine whether there are differences in ERα and ERβ expression in granulosa cells (GC) and theca cells (TC) from women with PCOS, compared with regularly cycling women. GC and TC were obtained by microdissection from 12 polycystic and 23 normal ovaries. ERα and ERβ mRNA and protein expression were measured by semiquantitative RT-PCR and Western blot, respectively. In control ovaries, both GC and TC ERα mRNAs were higher in small antral (SA) than in dominant follicles. ERα mRNA was similar in PCOS and size-matched control follicles. In control follicles, ERα protein concentrations were higher in GC than in TC. In GC, the ERα concentrations were comparable among SA, dominant, and PCOS follicles. In TC, ERα concentrations were lower in dominant follicles but were markedly increased in PCOS. In control ovaries, GC and TC expression of ERβ mRNA was higher in SA, compared with dominant follicles. In PCOS, ERβ mRNA was intermediate between SA and dominant follicles in both GC and TC. In GC, the ERβ protein concentrations followed the same pattern as mRNA expression; but in TC ERβ, protein in PCOS was equivalent to that in dominant follicles. The results of this study demonstrate that there are significant alterations in the expression of ERα and ERβ in PCOS that may be related to abnormal follicular development.

Cite

CITATION STYLE

APA

Jakimiuk, A. J., Weitsman, S. R., Yen, H. W., Bogusiewicz, M., & Magoffin, D. A. (2002). Estrogen receptor α and β expression in theca and granulosa cells from women with polycystic ovary syndrome. Journal of Clinical Endocrinology and Metabolism, 87(12), 5532–5538. https://doi.org/10.1210/jc.2002-020323

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free