| Literature DB >> 18818360 |
Christopher S Rogers1, David A Stoltz, David K Meyerholz, Lynda S Ostedgaard, Tatiana Rokhlina, Peter J Taft, Mark P Rogan, Alejandro A Pezzulo, Philip H Karp, Omar A Itani, Amanda C Kabel, Christine L Wohlford-Lenane, Greg J Davis, Robert A Hanfland, Tony L Smith, Melissa Samuel, David Wax, Clifton N Murphy, August Rieke, Kristin Whitworth, Aliye Uc, Timothy D Starner, Kim A Brogden, Joel Shilyansky, Paul B McCray, Joseph Zabner, Randall S Prather, Michael J Welsh.
Abstract
Almost two decades after CFTR was identified as the gene responsible for cystic fibrosis (CF), we still lack answers to many questions about the pathogenesis of the disease, and it remains incurable. Mice with a disrupted CFTR gene have greatly facilitated CF studies, but the mutant mice do not develop the characteristic manifestations of human CF, including abnormalities of the pancreas, lung, intestine, liver, and other organs. Because pigs share many anatomical and physiological features with humans, we generated pigs with a targeted disruption of both CFTR alleles. Newborn pigs lacking CFTR exhibited defective chloride transport and developed meconium ileus, exocrine pancreatic destruction, and focal biliary cirrhosis, replicating abnormalities seen in newborn humans with CF. The pig model may provide opportunities to address persistent questions about CF pathogenesis and accelerate discovery of strategies for prevention and treatment.Entities:
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Year: 2008 PMID: 18818360 PMCID: PMC2570747 DOI: 10.1126/science.1163600
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728