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Am J Physiol Lung Cell Mol Physiol 296: L145-L155, 2009. First published December 5, 2008; doi:10.1152/ajplung.90525.2008
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REVIEW

Molecular diversity and function of K+ channels in airway and alveolar epithelial cells

Olivier Bardou,1,2 Nguyen Thu Ngan Trinh,1,2 and Emmanuelle Brochiero1,2

1Centre de Recherche, Centre Hospitalier de l'Université de Montréal (CRCHUM), Hôtel-Dieu and 2Départment de médecine, Université de Montréal, Montréal, Québec, Canada

ABSTRACT

Multiple K+ channels are expressed in the respiratory epithelium lining airways and alveoli. Of the three main classes [1) voltage-dependent or Ca2+-activated, 6-transmembrane domains (TMD), 2) 2-pores 4-TMD, and 3) inward-rectified 2-TMD K+ channels], almost 40 different transcripts have already been detected in the lung. The physiological and functional significance of this high molecular diversity of lung epithelial K+ channels is intriguing. As detailed in the present review, K+ channels are located at both the apical and basolateral membranes in the respiratory epithelium, where they mediate K+ currents of diverse electrophysiological and regulatory properties. The main recognized function of K+ channels is to control membrane potential and to maintain the driving force for transepithelial ion and liquid transport. In this manner, KvLQT1, KCa and KATP channels, for example, contribute to the control of airway and alveolar surface liquid composition and volume. Thus, K+ channel activation has been identified as a potential therapeutic strategy for the resolution of pathologies characterized by ion transport dysfunction. K+ channels are also involved in other key functions in lung physiology, such as oxygen-sensing, inflammatory responses and respiratory epithelia repair after injury. The purpose of this review is to summarize and discuss what is presently known about the molecular identity of lung K+ channels with emphasis on their role in lung epithelial physiology.

Kv channels; KCa channels; Kir channels; K2P channels; lung; ion transport; epithelial repair; oxygen sensing; inflammation



Address for reprint requests and other correspondence: E. Brochiero, Centre de recherche du CHUM, Hôtel-Dieu, 3840, Saint-Urbain, Montréal, Québec H2W 1T8, Canada (e-mail: emmanuelle.brochiero{at}umontreal.ca)







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