Importance of ENaC-Mediated Sodium Transport in Alveolar Fluid Clearance Using Genetically-Engineered Mice

被引:47
作者
Hummler, Edith [1 ]
Planes, Carole [2 ]
机构
[1] Univ Lausanne, Dept Pharmacol & Toxicol, CH-1005 Lausanne, Switzerland
[2] Univ Paris 13, UFR Sante, EA2363, Bobigny, France
基金
瑞士国家科学基金会;
关键词
Epithelial sodium channel; ENaC; CAP1; Channel-activating protease; Edema; Transgenic mice; EPITHELIAL NA+ CHANNEL; RESPIRATORY-DISTRESS SYNDROME; HYDROSTATIC PULMONARY-EDEMA; EPIDERMAL BARRIER FUNCTION; LUNG LIQUID CLEARANCE; MOUSE MODEL; LIDDLES-SYNDROME; CYSTIC-FIBROSIS; ALPHA-ENAC; ION-TRANSPORT;
D O I
10.1159/000272051
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The lung possesses specific transport systems that intra- and extracellularly maintain salt and fluid balance necessary for its function. At birth, the lungs rapidly transform into a fluid (Na(+))-absorbing organ to enable efficient gas exchange. Alveolar fluid clearance, which mainly depends on sodium transport in alveolar epithelial cells, is an important mechanism by which excess water in the alveoli is reabsorbed during the resolution of pulmonary edema. In this review, we will focus and summarize on the role of ENaC in alveolar lung liquid clearance and discuss recent data from mouse models with altered activity of epithelial sodium channel function in the lung, and more specifically in alveolar fluid clearance. Recent data studying mice with hyperactivity of ENaC or mice with reduced ENaC activity clearly illustrate the impaired lung fluid clearance in these adult mice. Further understanding of the physiological role of ENaC and its regulatory proteins implicated in salt and water balance in the alveolar cells may therefore help to develop new therapeutic strategies to improve gas exchange in pulmonary edema. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:63 / 70
页数:8
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