| First Author | Gustafsson JK | Year | 2012 |
| Journal | J Exp Med | Volume | 209 |
| Issue | 7 | Pages | 1263-72 |
| PubMed ID | 22711878 | Mgi Jnum | J:189205 |
| Mgi Id | MGI:5444603 | Doi | 10.1084/jem.20120562 |
| Citation | Gustafsson JK, et al. (2012) Bicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype. J Exp Med 209(7):1263-72 |
| abstractText | Cystic fibrosis (CF) is caused by a nonfunctional chloride and bicarbonate ion channel (CF transmembrane regulator [CFTR]), but the link to the phenomenon of stagnant mucus is not well understood. Mice lacking functional CFTR (CftrDelta508) have no lung phenotype but show similar ileal problems to humans. We show that the ileal mucosa in CF have a mucus that adhered to the epithelium, was denser, and was less penetrable than that of wild-type mice. The properties of the ileal mucus of CF mice were normalized by secretion into a high concentration sodium bicarbonate buffer (~100 mM). In addition, bicarbonate added to already formed CF mucus almost completely restored the mucus properties. This knowledge may provide novel therapeutic options for CF. |
