Journal
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY
Volume 288, Issue 5, Pages L813-L819Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajplung.00435.2004
Keywords
silent channels; cystic fibrosis; serine protease; elastase
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Funding
- NHLBI NIH HHS [HL-60280] Funding Source: Medline
- NIDDK NIH HHS [DK-67103] Funding Source: Medline
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Neutrophil elastase is a serine protease that is abundant in the airways of individuals with cystic fibrosis (CF), a genetic disease manifested by excessive airway Na+ absorption and consequent depletion of the airway surface liquid layer. Although endogenous epithelium-derived serine proteases regulate epithelial Na+ transport, the effects of neutrophil elastase on epithelial Na+ transport and epithelial Na+ channel (ENaC) activity are unknown. Low micromolar concentrations of human neutrophil elastase (hNE) applied to the apical surface of a human bronchial cell line (16HBE14o-/beta gamma) increased Na+ transport about twofold. Similar effects were observed with trypsin, also a serine protease. Proteolytic inhibitors of hNE or trypsin selectively abolished the enzyme-induced increase of epithelial Na+ transport. At the level of the single channel, submicromolar concentrations of hNE increased activity of near-silent ENaC similar to 108-fold in patches from NIH-3T3 cells expressing rat alpha-, beta-, and gamma-ENaC subunits. However, no enzyme effects were observed on basally active ENaCs. Trypsin exposure following hNE revealed no additional increase in amiloride-sensitive short-circuit current or in ENaC activity, suggesting these enzymes share a common mode of action for increasing Na+ transport, likely through proteolytic activation of ENaC. The hNE-induced increase of near-silent ENaC activity in CF airways could contribute to Na+ hyperabsorption, reduced airway surface liquid height, and dehydrated mucus culminating in inefficient mucociliary clearance.
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