Biol Reprod Lalor Postdoctoral Fellowships -- Application Deadline January 15, 2009
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


BOR - Papers in Press, published online ahead of print October 23, 2002.
Biol Reprod 2002, 10.1095/biolreprod.102.009605
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
68/3/867    most recent
biolreprod.102.009605v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Thuillier, R.
Right arrow Articles by Culty, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Thuillier, R.
Right arrow Articles by Culty, M.
Agricola
Right arrow Articles by Thuillier, R.
Right arrow Articles by Culty, M.
Submitted July 21, 2002
Returned for revision August 15, 2002
Accepted September 19, 2002

Testis


Prenatal Exposure to Estrogenic Compounds Alters the Expression Pattern of Platelet-Derived Growth Factor Receptors {alpha} and ß in Neonatal Rat Testis: Identification of Gonocytes as Targets of Estrogen Exposure

Raphael Thuillier 1, Yan Wang 1, Martine Culty 2*
1 Georgetown University
2 Georgetown University School of Medicine

* To whom correspondence should be addressed. E-mail: cultym{at}aol.com.

Abstract

We examined the effects of maternal exposure to estrogens on platelet-derived growth factor (PDGF) receptor expression in newborn rat testis. Pregnant rats were treated from gestation day 14 to birth with corn oil containing diethylstilbestrol, bisphenol A, genistein or coumestrol, by gavage or subcutaneous injection. These treatments induced a dose-dependent increase in the expression of PDGF receptor (PDGFR) {alpha} and ß mRNAs, determined by semiquantitative RT-PCR, though DES had a biphasic effect on both mRNAs. In situ hybridization analysis showed that PDGFR{alpha} mRNA increased mostly in the interstitium, while PDGFRß mRNA increased both in the interstitium and seminiferous cords. mmunohistochemical studies of PDGFR {alpha} and ß proteins revealed that both receptors were present in testis before and after birth, and that they were upregulated upon treatment with estrogens in 3-day-old rats, with PDGFRß increasing dramatically in gonocytes. PDGFR {alpha} and ß mRNAs and proteins were also found in purified gonocytes. Our previous finding that PDGF and 17ß-estradiol induce gonocyte proliferation in vitro, together with the present finding that in vivo exposure to estrogens upregulates PDGF receptors in testis, suggest that PDGF pathway is a target of estrogens in testis. In addition, these data identify PDGFRß in gonocytes as a major target of gestational estrogen exposure, suggesting that estrogen may have a physiological interaction with PDGF during gonocyte development. These results however, do not exclude the possibility that the effects of the compounds examined in this study might be due to estrogen receptor-independent action(s).



Key words: Testis • Toxicology • Estradiol • Growth factors • Spermatogenesis






HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2002 by the Society for the Study of Reproduction.