Prostaglandin E2 receptor expression in fetal baboon lung at 0.7 gestation after betamethasone exposure

The fetal lung produces and metabolizes prostaglandin (PG) E-2. In vitro PGE(2) induces surfactant production via E prostaglandin (EP)(1) and cyclic adenosine monophosphate (cAMP)coupled EP (EP2 and EP4) receptors. Glucocorticoids alter PG function and increase lung function in preterm neonates. We hypothesized that fetal exposure to maternally administered betamethasone (beta M) enhances fetal lung EP, and cAMP-coupled EP receptor expression. Pregnant baboons were injected intramuscularly (i.m.) with either beta M (n = 7) or saline [control (CTR); n = 8] at 0.7 gestation. Fetal lungs were removed at cesarean section 48 It after the first injection. We determined mRNA levels, protein localization and abundance for all four PGE(2) receptors by real-time polymerase chain reaction (PCR), immunohistochemistry, and Western blot. EP receptors were widely distributed in bronchiolar epithelium, bronchiolar smooth muscle, and endothelium and media of blood vessels, but not alveoli. Compared with CTR, PM exposure resulted in a twofold EP2 mRNA decrease (p < 0.05) in male fetuses only. EP1, EP3, and EP4 receptor mRNA levels were unaffected. Western blot analysis showed no alteration in EP receptor protein expression. In summary, this is the first demonstration of the four EP receptors in fetal lung. The only change after 48-h beta M exposure was a gender-specific decrease in EP2 receptor mRNA.