Smad 3 may regulate follicular growth in the mouse ovary

D. Tomic, S. G. Brodie, C. Deng, R. J. Hickey, J. K. Babus, L. H. Malkas, Jodi A. Flaws

Research output: Contribution to journalArticlepeer-review

Abstract

Although Smad 3 is known to serve as a signaling intermediate for the transforming growth factor beta (TGFβ) family in nonreproductive tissues, its role in the ovary is unknown. Thus, we used a recently generated Smad 3-deficient (Smad 3-/-) mouse model to test the hypothesis that Smad 3 alters female fertility and regulates the growth of ovarian follicles from the primordial stage to the antral stage. In addition, we tested whether Smad 3 affects the levels of proteins that control apoptosis, survival, and proliferation in the ovarian follicle. To test this hypothesis, breeding studies were conducted using Smad 3-/- and wild-type mice. In addition, ovaries were collected from Smad 3-/- and wild-type mice on Postnatal Days 2-90. One ovary from each animal was used to estimate the total number of primordial, primary, and antral follicles. The other ovary was used for immunohistochemical analysis of selected members of the B-cell lymphoma/leukemia-2 family of protooncogenes (Bax, Bcl-2, Bcl-x), proliferating cell nuclear antigen (PCNA), and cyclin-dependent kinase 2 (Cdk-2). The results indicate that Smad 3-/- mice have reduced fertility compared with wild type mice. The results also indicate that Smad 3 may not affect the size of the primordial follicle pool at birth, but it may regulate growth of primordial follicles to the antral stage. Further, the results indicate that Smad 3 may regulate the expression of Bax and Bcl-2, but not Bcl-x, Cdk-2, and PCNA. Collectively, these data suggest that Smad 3 may play an important role in the regulation of ovarian follicle growth and female fertility.

Original languageEnglish (US)
Pages (from-to)917-923
Number of pages7
JournalBiology of reproduction
Volume66
Issue number4
DOIs
StatePublished - 2002
Externally publishedYes

Keywords

  • Apoptosis
  • Follicle
  • Follicular development
  • Growth factors
  • Ovary

ASJC Scopus subject areas

  • Reproductive Medicine
  • Cell Biology

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