Endogenous tumor necrosis factor α mediates enhanced apoptosis of cultured villous trophoblasts from intrauterine growth-restricted placentae

Tumor necrosis factor alpha (TNF alpha) has been implicated in the abnormally high levels of trophoblast apoptosis seen in placentae from pregnancies complicated by small births. We examined the hypothesis that at physiological (35-50 mmHg) oxygen tensions, the production of TNF alpha stimulates the apoptosis of placental trophoblasts associated with infants that are intrauterine growth-restricted (IUGR). Highly purified cytotrophoblasts (CT) from IUGR-complicated pregnancies spontaneously underwent a higher rate of apoptosis after 24 h of culture at a normoxic (for villous CT) tension of 38 mmHg than did CT from normal placentae. Real-time PCR analysis of TNF alpha mRNA revealed similar to threefold higher levels in ltJGR trophoblasts after culturing at a pO(2) of 38 mmHg. A higher level of TNF alpha receptor p55 (which mediates apoptosis) was found in IUGR CT by western blot analysis at pO(2) Of < 10, 38, and 140 mmHg. Neutralizing antibody to TNF alpha significantly inhibited the apoptosis of IUGR trophoblasts cultured at 38 mmHg and addition of TNF alpha significantly elevated apoptosis of normal and IUGR trophoblasts but less in IUGR cells cultured at < 10 mmHg. We conclude that at physiological oxygen tensions (38 mmHg), villous CT from IUGR pregnancies, when compared with uncomplicated pregnancies, undergo more TNF alpha-induced apoptosis both because of elevated expression of TNF alpha and TNF receptor p55.