The current study investigates the hypothesis that retinoids have a role in
embryonic testis development. The action of retinoids on testis developmen
t and the expression of retinoic acid receptors (RAR alpha, RAR beta, RAR g
amma) were examined. In embryonic day 13 (E13; plug date = EO) testis organ
cultures an RAR-selective agonist and alltrans retinoic acid completely in
hibited seminiferous cord formation. In contrast, an RAR alpha-selective an
tagonist had no effect. RT-PCR demonstrated that RAR alpha messenger RNA (m
RNA) was expressed at all developmental time points evaluated, which includ
ed embryonic day 14 (E14) through postnatal day 30 (P30). Expression of RAR
beta mRNA was present at E15 through P2, whereas RAR gamma mRNA was expres
sed at E18 through P2. Cellular localization of receptors by immunohistoche
mistry indicated that RARa was localized to the interstitium at E18 and to
the seminiferous cords by PO. RAR beta and RAR gamma were detected in both
interstitium and cords at E16 and by E18 were mainly expressed in the cords
. At PO RAR beta and RAR gamma were localized to the germ cell populations.
To examine retinoid actions, the growth of PO testis cultures were investi
gated. Interestingly, retinol and retinoic acid did not inhibit growth of P
O testis cultures but did inhibit the action of growth stimulators. Retinoi
c acid inhibited FSH, EGF, and 10% calf serum stimulated growth in PO testi
s cultures. The hypothesis tested was that the inhibitory effects of retino
ids on PO testis growth may be mediated through the growth inhibitor, trans
forming growth factor-beta TGF beta. The action of retinoids on TGF beta mR
NA expression was examined in PO testis cultures. Retinoic acid stimulated
TGF beta 3 mRNA expression within 24 h and increased expression of TGF beta
1 and TGF beta 2 after 72 h. Retinol increased expression of TGF beta 1 an
d TGF beta 2 but not TGF beta 3 after 72 h of treatment. These observations
indicate that retinoic acid can influence seminiferous cord formation and
testis growth. The inhibitory actions of retinoids may in part be mediated
through increased expression of TGF beta isoforms.