Hormone-regulated expression and distribution of versican in mouse uterine tissues

Abstract Background Remodeling of the extracellular matrix is one of the most striking features observed in the uterus during the estrous cycle and after hormone replacement. Versican (VER) is a hyaluronan-binding proteoglycan that undergoes RNA alternative splicing, generating four distinct isoforms. This study analyzed the synthesis and distribution of VER in mouse uterine tissues during the estrous cycle, in ovariectomized (OVX) animals and after 17beta-estradiol (E2) and medroxyprogesterone (MPA) treatments, either alone or in combination. Methods Uteri from mice in all phases of the estrous cycle, and animals subjected to ovariectomy and hormone replacement were collected for immunoperoxidase staining for versican, as well as PCR and quantitative Real Time PCR. Results In diestrus and proestrus, VER was exclusively expressed in the endometrial stroma. In estrus and metaestrus, VER was present in both endometrial stroma and myometrium. In OVX mice, VER immunoreaction was abolished in all uterine tissues. VER expression was restored by E2, MPA and E2+MPA treatments. Real Time PCR analysis showed that VER expression increases considerably in the MPA-treated group. Analysis of mRNA identified isoforms V0, V1 and V3 in the mouse uterus. Conclusion These results show that the expression of versican in uterine tissues is modulated by ovarian steroid hormones, in a tissue-specific manner. VER is induced in the myometrium exclusively by E2, whereas MPA induces VER deposition only in the endometrial stroma.

This study was carried out as partial fulfillment of a PhD degree by Renato M Salgado (advisor: TMT Zorn) and was supported by a fellowship from FAPESP (04/09947-2) and grants from FAPESP, CAPES and CNPq. The authors are grateful to Mrs. Fernanda C Barrence, Mrs. Fernanda F Fernandes and Dr Karin Spiess for the excellent technical assistance. The authors are also thankful for the important suggestions given by the peer reviewers.

This study was carried out as partial fulfillment of a PhD degree by Renato M Salgado (advisor: TMT Zorn) and was supported by a fellowship from FAPESP (04/099472) and grants from FAPESP, CAPES and CNPq. The authors are grateful to Mrs. Fernanda C Barrence, Mrs. Fernanda F Fernandes and Dr Karin Spiess for the excellent technical assistance. The authors are also thankful for the important suggestions given by the peer reviewers.