| Literature DB >> 12845704 |
Daniel Symonds1, Dragana Tomic, Christina Borgeest, Elizabeth McGee, Jodi A Flaws.
Abstract
Smad 3 is a signaling intermediate for the transforming growth factor beta (TGFbeta) family; however, little is known about the role this protein plays in the regulation of the ovarian surface epithelium (OSE). Using a transgenic mouse model, we found that in the absence of Smad 3 there was a distinct morphological alteration of OSE cells. Wild-type (WT) OSE was flat with thin cells, while Smad 3-deficient (Smad 3 -/-) OSE was thick with plump cuboidal cells. WT OSE had less immunostaining for proliferating cell nuclear antigen (PCNA) and estrogen receptor alpha (ERalpha) than Smad 3 -/- OSE. However, there were no differences in the number of apoptotic cells or Bax and Bcl-2 levels between WT and Smad 3 -/- OSE. Although WT mice had higher levels of serum estradiol than Smad 3 -/- mice, WT and Smad 3 -/- mice had similar levels of progesterone. These data suggest that Smad 3 regulates OSE morphological appearance and proliferation in the absence of high serum estradiol levels or alterations in progesterone levels. Copyright 2003 Wiley-Liss, Inc.Entities:
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Year: 2003 PMID: 12845704 DOI: 10.1002/ar.a.10090
Source DB: PubMed Journal: Anat Rec A Discov Mol Cell Evol Biol ISSN: 1552-4884