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Puzzle resolved: CFTR mediates chloride homeostasis by segregating absorption and secretion to different cell types
In the lungs, the cystic fibrosis transmembrane conductance regulator (CFTR) regulates ion transport in surface-airway epithelia and submucosal glands, thus determining airway surface liquid (ASL) volume and mucus hydration. In this issue of the JCI, Lei Lei and colleagues report that the CFTR-rich...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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American Society for Clinical Investigation
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10575718/ https://www.ncbi.nlm.nih.gov/pubmed/37843282 http://dx.doi.org/10.1172/JCI174667 |