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
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)
and ß
mRNAs, determined by semiquantitative RT-PCR, though DES
had a biphasic effect on both mRNAs. In situ hybridization
analysis showed that PDGFR
mRNA increased mostly
in the interstitium, while PDGFRß mRNA increased
both in the interstitium and seminiferous cords.
mmunohistochemical studies of PDGFR
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
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