Localization of Cardiac Sodium Channels in Caveolin-Rich Membrane DomainsRegulation of Sodium Current Amplitude
作者:
Tracy Yarbrough,
Tong Lu,
Hon-Chi Lee,
Erwin Shibata,
期刊:
Circulation Research: Journal of the American Heart Association
(OVID Available online 2002)
卷期:
Volume 90,
issue 4
页码: 443-449
ISSN:0009-7330
年代: 2002
出版商: OVID
关键词: caveolae;ion channel;signal transduction;cardiac;adrenergic
数据来源: OVID
摘要:
This study demonstrates that caveolae, omega-shaped membrane invaginations, are involved in cardiac sodium channel regulation by a mechanism involving the &agr; subunit of the stimulatory heterotrimeric G-protein, G&agr;s, via stimulation of the cell surface &bgr;-adrenergic receptor. Stimulation of &bgr;-adrenergic receptors with 10 &mgr;mol/L isoproterenol in the presence of a protein kinase A inhibitor increased the whole-cell sodium current by a “direct” cAMP-independent G-protein mechanism. The addition of antibodies against caveolin-3 to the cell’s cytoplasm via the pipette solution abrogated this direct G protein-induced increase in sodium current, whereas antibodies to caveolin-1 or caveolin-2 did not. Voltage-gated sodium channel proteins were found to associate with caveolin-rich membranes obtained by detergent-free buoyant density separation. The purity of the caveolar membrane fraction was verified by Western blot analyses, which indicated that endoplasmic/sarcoplasmic reticulum, endosomal compartments, Golgi apparatus, clathrin-coated vesicles, and sarcolemmal membranes were excluded from the caveolin-rich membrane fraction. Additionally, the sodium channel was found to colocalize with caveolar membranes by immunoprecipitation, indirect immunofluorescence, and immunogold transmission electron microscopy. These results suggest that stimulation of &bgr;-adrenergic receptors, and thereby G&agr;s, promotes the presentation of cardiac sodium channels associated with caveolar membranes to the sarcolemma.
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