Journal article
Cystic Fibrosis Airway Epithelia Fail to Kill Bacteria Because of Abnormal Airway Surface Fluid
Cell (Cambridge), Vol.85(2), pp.229-236
04/1996
DOI: 10.1016/S0092-8674(00)81099-5
PMID: 8612275
Abstract
Despite an increased understanding of the cellular and molecular biology of the CFTR Cl− channel, it is not known how defective Cl− transport across airway epithelia causes chronic bacterial infections in cystic fibrosis (CF) airways. Here, we show that common CF pathogens were killed when added to the apical surface of normal airway epithelia. In contrast, these bacteria multiplied on CF epithelia. We found that bactericidal activity was present in airway surface fluid of both normal and CF epithelia. However, because bacterial killing required a low NaCl concentration and because CF surface fluid has a high NaCl concentration, CF epithelia failed to kill bacteria. This defect was corrected by reducing the NaCl concentration on CF epithelia. These data explain how the loss of CFTR Cl− channels may lead to lung disease and suggest new approaches to therapy.
Details
- Title: Subtitle
- Cystic Fibrosis Airway Epithelia Fail to Kill Bacteria Because of Abnormal Airway Surface Fluid
- Creators
- Jeffrey J SmithSue M TravisE.Peter GreenbergMichael J Welsh
- Resource Type
- Journal article
- Publication Details
- Cell (Cambridge), Vol.85(2), pp.229-236
- DOI
- 10.1016/S0092-8674(00)81099-5
- PMID
- 8612275
- ISSN
- 0092-8674
- eISSN
- 1097-4172
- Language
- English
- Date published
- 04/1996
- Academic Unit
- Neurology; Molecular Physiology and Biophysics; Pulmonary, Critical Care, and Occupational Medicine; Stead Family Department of Pediatrics; Neurosurgery; Internal Medicine
- Record Identifier
- 9984020896702771
Metrics
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