Heterogeneity of hypoxia-mediated decrease in IK(V) and increase in [Ca ]cyt in pulmonary artery smooth muscle cells

Platoshyn O, Yu Y, Ko EA, Remillard CV, Yuan JX. Heterogeneity of hypoxia-mediated decrease in IK(V) and increase in [Ca ]cyt in pulmonary artery smooth muscle cells. Am J Physiol Lung Cell Mol Physiol 293: L402–L416, 2007. First published May 25, 2007; doi:10.1152/ajplung.00391.2006.—Hypoxic pulmonary vasoconstriction is caused by a rise in cytosolic Ca ([Ca ]cyt) in pulmonary artery smooth muscle cells (PASMC) via multiple mechanisms. PASMC consist of heterogeneous phenotypes defined by contractility, proliferation, and apoptosis as well as by differences in expression and function of various genes. In rat PASMC, hypoxia-mediated decrease in voltage-gated K (Kv) currents (IK(V)) and increase in [Ca ]cyt were not uniformly distributed in all PASMC tested. Acute hypoxia decreased IK(V) and increased [Ca ]cyt in 46% and 53% of PASMC, respectively. Using combined techniques of single-cell RTPCR and patch clamp, we show here that mRNA expression level of Kv1.5 in hypoxia-sensitive PASMC (in which hypoxia reduced IK(V)) was much greater than in hypoxia-insensitive cells (in which hypoxia negligibly affected IK(V)). These results demonstrate that 1) different PASMC express different Kv channel and -subunits, and 2) the sensitivity of a PASMC to acute hypoxia partially depends on the expression level of Kv1.5 channels; hypoxia reduces whole-cell IK(V) only in PASMC that express high level of Kv1.5. In addition, the acute hypoxia-mediated changes in [Ca ]cyt also vary in different PASMC. Hypoxia increases [Ca ]cyt only in 34% of cells tested, and the different sensitivity of [Ca ]cyt to hypoxia was not related to the resting [Ca ]cyt. An intrinsic mechanism within each individual cell may be involved in the heterogeneity of hypoxia-mediated effect on [Ca ]cyt in PASMC. These data suggest that the heterogeneity of PASMC may partially be related to different expression levels and functional sensitivity of Kv channels to hypoxia and to differences in intrinsic mechanisms involved in regulating [Ca ]cyt.