Activation of protein kinase C alters the intracellular distribution and mobility of cardiac Na+ channels.

Hallaq H, Wang DW, Kunic JD, George AL, Wells KS, Murray KT
Am J Physiol Heart Circ Physiol. 2012 302 (3): H782-9

PMID: 22101522 · PMCID: PMC3353784 · DOI:10.1152/ajpheart.00817.2010

Na(+) current derived from expression of the cardiac isoform SCN5A is reduced by receptor-mediated or direct activation of protein kinase C (PKC). Previous work has suggested a possible role for loss of Na(+) channels at the plasma membrane in this effect, but the results are controversial. In this study, we tested the hypothesis that PKC activation acutely modulates the intracellular distribution of SCN5A channels and that this effect can be visualized in living cells. In human embryonic kidney cells that stably expressed SCN5A with green fluorescent protein (GFP) fused to the channel COOH-terminus (SCN5A-GFP), Na(+) currents were suppressed by an exposure to PKC activation. Using confocal microscopy, colocalization of SCN5A-GFP channels with the plasma membrane under control and stimulated conditions was quantified. A separate population of SCN5A channels containing an extracellular epitope was immunolabeled to permit temporally stable labeling of the plasma membrane. Our results demonstrated that Na(+) channels were preferentially trafficked away from the plasma membrane by PKC activation, with a major contribution by Ca(2+)-sensitive or conventional PKC isoforms, whereas stimulation of protein kinase A (PKA) had the opposite effect. Removal of the conserved PKC site Ser(1503) or exposure to the NADPH oxidase inhibitor apocynin eliminated the PKC-mediated effect to alter channel trafficking, indicating that both channel phosphorylation and ROS were required. Experiments using fluorescence recovery after photobleaching demonstrated that both PKC and PKA also modified channel mobility in a manner consistent with the dynamics of channel distribution. These results demonstrate that the activation of protein kinases can acutely regulate the intracellular distribution and molecular mobility of cardiac Na(+) channels in living cells.

MeSH Terms (14)

Calcium Cell Membrane Cyclic AMP-Dependent Protein Kinases Enzyme Activation Green Fluorescent Proteins HEK293 Cells Humans Membrane Potentials Myocardial Contraction Myocardium NAV1.5 Voltage-Gated Sodium Channel Protein Kinase C Protein Transport Sodium Channels

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