Journal article
Authors list: Hollenhorst, Monika I.; Richter, Katrin; Fronius, Martin
Publication year: 2011
Journal: Journal of Biomedicine and Biotechnology
Volume number: 2011
Issue number: 1
ISSN: 1110-7243
eISSN: 1110-7251
Open access status: Hybrid
DOI Link: https://doi.org/10.1155/2011/174306
Publisher: Hindawi
Abstract:
The lung surface of air-breathing vertebrates is formed by a continuous epithelium that is covered by a fluid layer. In the airways, this epitheliumis largely pseudostratified consisting of diverse cell types such as ciliated cells, goblet cells, and undifferentiated basal cells, whereas the alveolar epitheliumconsists of alveolar type I and alveolar type II cells. Regulation and maintenance of the volume and viscosity of the fluid layer covering the epithelium is one of the most important functions of the epithelial barrier that forms the outer surface area of the lungs. Therefore, the epithelial cells are equipped with a wide variety of ion transport proteins, among which Na+, Cl-, and K+ channels have been identified to play a role in the regulation of the fluid layer. Malfunctions of pulmonary epithelial ion transport processes and, thus, impairment of the liquid balance in our lungs is associated with severe diseases, such as cystic fibrosis and pulmonary oedema. Due to the important role of pulmonary epithelial ion transport processes for proper lung function, the present paper summarizes the recent findings about composition, function, and ion transport properties of the airway epithelium as well as of the alveolar epithelium.
Citation Styles
Harvard Citation style: Hollenhorst, M., Richter, K. and Fronius, M. (2011) Ion Transport by Pulmonary Epithelia, Journal of Biomedicine and Biotechnology, 2011(1), Article 174306. https://doi.org/10.1155/2011/174306
APA Citation style: Hollenhorst, M., Richter, K., & Fronius, M. (2011). Ion Transport by Pulmonary Epithelia. Journal of Biomedicine and Biotechnology. 2011(1), Article 174306. https://doi.org/10.1155/2011/174306
Keywords
acute lung injury; BASOLATERAL CL-CHANNELS; CYSTIC-FIBROSIS; EDEMA FLUID CLEARANCE; II CELLS; K-ATP CHANNELS; MESENCHYMAL STEM-CELLS; SELECTIVE SODIUM-CHANNELS; TRANSMEMBRANE CONDUCTANCE REGULATOR