Am J Physiol Lung Cell Mol Physiol
June 2004
In excitable cells, hypoxia inhibits K channels, causes membrane depolarization, and initiates complex adaptive mechanisms. It is unclear whether K channels of alveolar epithelial cells reveal a similar response to hypoxia. A549 cells were exposed to hypoxia during whole cell patch-clamp measurements.
View Article and Find Full Text PDFCell Physiol Biochem
October 2001
In excitatory cells specific responses upon changes in PO(2) are mediated by changes in intracellular Ca (Ca(i)). We wanted to know whether ion transport of lung alveolar epithelial cells is regulated by Ca(i) and whether Ca(i) and Ca(i) -signaling are affected by hypoxia in a way that might explain hypoxic transport inhibition (Mairbäurl et al. AJP 273: L797, 1997).
View Article and Find Full Text PDFFluid reabsorption from alveolar space is driven by active Na reabsorption via epithelial Na channels (ENaCs) and Na-K-ATPase. Both are inhibited by hypoxia. Here we tested whether hypoxia decreases Na transport by decreasing the number of copies of transporters in alveolar epithelial cells and in lungs of hypoxic rats.
View Article and Find Full Text PDFAm J Physiol Lung Cell Mol Physiol
April 2000
In oxygen-sensitive excitable cells, responses to hypoxia are initiated by membrane depolarization due to closing of the K channels that is thought to be mediated by a decrease in reactive oxygen species (ROS). Because the mechanisms of hypoxic inhibition of ion transport of alveolar epithelial cells (Planes C, Friedlander G, Loiseau A, Amiel C, and Clerici C. Am J Physiol Lung Cell Mol Physiol 271: L70-L78, 1996; Mairbäurl H, Wodopia R, Eckes S, Schulz S, and Bärtsch P.
View Article and Find Full Text PDFJ Histochem Cytochem
September 1999
Peroxisomes in the human hepatoblastoma cell line HepG2 exhibit a high degree of plasticity. Whereas in confluent cultures they appear as small (0.1-0.
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