Journal article
CFTR-deficient pigs display peripheral nervous system defects at birth
LR Reznikov, Q Dong, JH Chen, TO Moninger, JM Park, Y Zhang, J Du, MS Hildebrand, RJH Smith, CO Randak, DA Stoltz, MJ Welsh
Proceedings of the National Academy of Sciences of the United States of America | Published : 2013
Abstract
Peripheral nervous system abnormalities, including neuropathy, have been reported in people with cystic fibrosis. These abnormalities have largely been attributed to secondary manifestations of the disease. We tested the hypothesis that disruption of the cystic fibrosis transmembrane conductance regulator (CFTR) gene directly influences nervous system function by studying newborn CFTR-/- pigs. We discovered CFTR expression and activity in Schwann cells, and loss of CFTR caused ultrastructural myelin sheath abnormalities similar to those in known neuropathies. Consistent with neuropathic changes, we found increased transcripts for myelin protein zero, a gene that, when mutated, can cause axon..
View full abstractGrants
Awarded by National Heart, Lung, and Blood Institute
Funding Acknowledgements
We thank Ricky Bahner, Tania Rokhlina, Paula Ludwig, Alex Tucker, Theresa Mayhew, Martin Cassell, David Meyerholz, and Lynda S. Ostegaard for help and advice. This work was supported by the National Heart, Lung, and Blood Institute (HL91842 and T32HL007121-36) and the Cystic Fibrosis Foundation. M.J.W. is an Investigator of the Howard Hughes Medical Institute.