Abstract
Congenital diaphragmatic hernia (CDH) leads to profound and often fatal pulmonary hypoplasia. However the mechanism by which growth is inhibited at a cellular level is not known. The epidermal growth factor family is believed to have a significant role in fetal lung growth. We investigated whether alterations in expression in this growth factor family may play a role in pulmonary hypoplasia in CDH. We used a fetal rat model of CDH induced by administering 2,4, dichlorophenyl-p-nitrophenyl ether (Nitrofen) to 7 pregnant rat mothers on day 11 of a 21 day gestation. The lungs were harvested on day 21 and compared to littermates without CDH. We performed RT-PCR on the mRNA of the CDH and non-CDH lungs for epidermal growth factor (EGF), transforming growth factor α (TGFα), and their receptor, epidermal growth factor receptor (EGFR). The PCR bands were normalized to β actin PCR bands and converted to densitometric units. The data are mean±s.e.m. and were compared by paired t-tests.
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