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.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.