4.5 Article

Mullerian inhibitory substance induces growth of rat preantral ovarian follicles

期刊

BIOLOGY OF REPRODUCTION
卷 64, 期 1, 页码 293-298

出版社

OXFORD UNIV PRESS INC
DOI: 10.1095/biolreprod64.1.293

关键词

activin; apoptosis; developmental biology; follicle; follicular development; FSH; gene regulation; granulosa cells; growth factors; hormone action; inhibin; ovary; signal transduction; theca cells

资金

  1. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT [U54HD031398] Funding Source: NIH RePORTER
  2. NICHD NIH HHS [HD31398, K12-HD-0084908] Funding Source: Medline

向作者/读者索取更多资源

Mullerian inhibitory substance (MIS), also known as anti-Mullerian hormone, is best known as the hormone that regulates the regression of the Mullerian duct in males. In females, MIS is expressed in granulosa cells of preantral and early antral follicles. The specific MIS type II receptor is present in granulosa and theca cells of these small, growing follicles. Because the role of MIS in preantral follicle development is unknown, we have evaluated the effect of MIS on the growth, differentiation, and apoptosis of intact preantral follicles in a serum-free culture system. In this system, treatment with FSH induces an increase in both follicle diameter, cell number, and follicle cell differentiation based on increased inhibin-alpha synthesis. Of interest, treatment with MIS enhances the effect of FSH both on follicle diameter and cell number. Although treatment with activin A also enhances FSH effects on follicle growth, treatment with transforming growth factor (TGF)-beta inhibits the FSH effects on follicle growth. Based on in situ staining of fragmented DNA, MIS was found to have no effect on follicle cell apoptosis, unlike its proapoptotic action on Mullerian ducts. In contrast to MIS and activin, TGF-beta was a potent proapoptotic factor for preantral follicles in culture. Analysis of inhibin-alpha expression of cultured preantral follicles further indicated that in contrast to activin, treatment with MIS did not enhance FSH-stimulated follicle differentiation. Thus, MIS is a unique factor that promotes preantral follicle growth but not preantral follicle cell differentiation and apoptosis.

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