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Biology of Reproduction 63, 1331-1340 (2000)
© 2000 Society for the Study of Reproduction, Inc.


Regular Article TA

Estrogen Receptors {alpha} and ß in the Female Reproductive Tract of the Rat During the Estrous Cycle1

Hong Wanga, Håkan Erikssona, and Lena Sahlin2,a

a Division for Reproductive Endocrinology, Department of Woman and Child Health, Karolinska Institutet, Stockholm, Sweden

ABSTRACT

The action of steroid hormones is primarily mediated via a process that involves hormone binding to specific receptors in target cells, which leads to transcriptional activation of steroid-responsive genes and, subsequently, to a modification of cellular responses. The aim of the present study was to obtain information about the dynamics of the two types of estrogen receptors (ERs), {alpha} and ß, by comparing their concentration and distribution in the reproductive tract of the rat during the estrous cycle. Twenty-four 55- to 60-day-old female Sprague-Dawley rats were used. The stage of estrous cycle was determined by vaginal smear. ER{alpha} was the dominating subtype in uterus, oviduct, and cervix/vagina, with the distribution varying in stroma and epithelium during the estrous cycle. A low level of ER{alpha} mRNA was observed in ovarian stromal cells, with some scattered positive cells found among granulosa cells. ERß expression was observed in the different compartments of uterus and cervix/vagina, but cyclic variation during the estrous cycle was less evident than that of ER{alpha}. Only a few scattered cells that contained ERß mRNA were observed in oviduct. ERß mRNA was highly expressed in granulosa cells of developing follicles, with a weaker hybridization signal in new corpora lutea. Immunohistochemistry showed that protein levels of ER{alpha} and ERß have distinct specificity for tissues and cell types, similar to their respective levels of mRNA, as assessed by in situ hybridization. The precise physiological function and importance of ERß is still unclear. The relative physiological and pathological function of each ER subtype in the female reproductive tract remains to be further evaluated.

FOOTNOTES

First decision: 10 March 2000.

1 Supported by grants from the Swedish Medical Research Council (3972) (H.E., L.S.), Swedish Society for Medical Research (H.W.), Åke Wibergs Foundation (L.S.), Magn.Bergvalls Foundation (L.S.), and Karolinska Institutet.

2 Correspondence: Lena Sahlin, Division for Reproductive Endocrinology, Karolinska Hospital, L5:01, S-17176 Stockholm, Sweden. FAX: 46 8 51773485; lena.sahlin{at}kbh.ki.se




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