Modulation of small leucine-rich proteoglycans (SLRPs) expression in the mouse uterus by estradiol and progesterone
- PDF / 1,103,248 Bytes
- 13 Pages / 595.28 x 793.7 pts Page_size
- 59 Downloads / 142 Views
RESEARCH
Open Access
Modulation of small leucine-rich proteoglycans (SLRPs) expression in the mouse uterus by estradiol and progesterone Renato M Salgado, Rodolfo R Favaro, Telma MT Zorn*
Abstract Background: We have previously demonstrated that four members of the family of small leucine-richproteoglycans (SLRPs) of the extracellular matrix (ECM), named decorin, biglycan, lumican and fibromodulin, are deeply remodeled in mouse uterine tissues along the estrous cycle and early pregnancy. It is known that the combined action of estrogen (E2) and progesterone (P4) orchestrates the estrous cycle and prepares the endometrium for pregnancy, modulating synthesis, deposition and degradation of various molecules. Indeed, we showed that versican, another proteoglycan of the ECM, is under hormonal control in the uterine tissues. Methods: E2 and/or medroxiprogesterone acetate (MPA) were used to demonstrate, by real time PCR and immunoperoxidase staining, respectively, their effects on mRNA expression and protein deposition of these SLRPs, in the uterine tissues. Results: Decorin and lumican were constitutively expressed and deposited in the ECM in the absence of the ovarian hormones, whereas deposition of biglycan and fibromodulin were abolished from the uterine ECM in the non-treated group. Interestingly, ovariectomy promoted an increase in decorin, lumican and fibromodulin mRNA levels, while biglycan mRNA conspicuously decreased. Hormone replacement with E2 and/or MPA differentially modulates their expression and deposition. Conclusions: The patterns of expression of these SLRPs in the uterine tissues were found to be hormonedependent and uterine compartment-related. These results reinforce the existence of subpopulations of endometrial fibroblasts, localized into distinct functional uterine compartments, resembling the organization into basal and functional layers of the human endometrium.
Background The reproductive cycle of human and rodents is characterized by recurring morphophysiological changes in the reproductive organs. The combined action of estrogen (E2) and progesterone (P4) orchestrates the cycle and prepares the endometrium for pregnancy. In the mouse, the cycle is known as estrous cycle and is divided into four different phases, denominated proestrus, estrus, metaestrus and diestrus, each one presenting distinct morphological and molecular features [1]. E2 produced during estrus stimulates epithelial cell proliferation and synthesis of progesterone receptors (PR). On * Correspondence: [email protected] Laboratory of Reproductive and Extracellular Matrix Biology, Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil
the other hand, P4 inhibits epithelial proliferation and stimulates the multiplication of endometrial stromal cells [2,3]. Estrogen receptors (ER) and PR are transcription factors that regulate gene expression by direct binding to DNA regulatory sequences or by specific interactions with co-activators and/or co-repressor protei
Data Loading...
