Title of article
Prenatal Exposure to Estrogenic Compounds Alters the Expression Pattern of Platelet-Derived Growth Factor Receptors (alpha)and (beta) in Neonatal Rat Testis: Identification of Gonocytes as Targets of Estrogen Exposure
Author/Authors
Thuillier، Raphael نويسنده , , Culty، Martine نويسنده , , WANG، YAN نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2003
Pages
-866
From page
867
To page
0
Abstract
We examined the effects of maternal exposure to estrogens on platelet-derived growth factor (PDGF) receptor (PDGFR) 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 PDGFR (alpha)and (beta) mRNAs, determined by semiquantitative reverse transcription polymerase chain reaction, though diethylstilbestrol had a biphasic effect on both mRNAs. In situ hybridization analysis showed that PDGFR(alpha) mRNA increased mostly in the interstitium, while PDGFR(beta) mRNA increased both in the interstitium and seminiferous cords. Immunohistochemical studies of PDGFR(alpha) and (beta) 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 PDGFR(beta) increasing dramatically in gonocytes. PDGFR(alpha) and (beta) mRNAs and proteins were also found in purified gonocytes. Our previous finding that PDGF and 17(beta)-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 PDGFR(beta) 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 receptorindependent action(s).
Keywords
growth factors , spermatogenesis , testis , estradiol , Toxicology
Journal title
Biology of Reproduction
Serial Year
2003
Journal title
Biology of Reproduction
Record number
88941
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