© 2001 American Heart Association, Inc.
Cellular Biology |
Independent Regulation of Cardiac Kv4.3 Potassium Channel Expression by Angiotensin II and Phenylephrine
From the Department of Pharmacology (T.-T.Z., K.T., E.S.L.) and Cardiovascular Institute (A.F.R.S., C.Z.), School of Medicine, University of Pittsburgh, Pittsburgh, Pa.
Correspondence to Edwin S. Levitan, E1351 Biomedical Science Tower, Department of Pharmacology, University of Pittsburgh, Pittsburgh, PA 15261. E-mail levitan{at}server.pharm.pitt.edu
Abstract—Hypertrophied cardiac myocytes exhibit prolonged action potentials and decreased transient outward potassium current (Ito). Because Kv4.3 is a major contributor to Ito, we studied regulation of its expression in neonatal rat cardiac myocytes in response to the known stimulators of cardiac myocyte hypertrophy, angiotensin II (Ang II) and phenylephrine (PE). RNase protection assays and immunoblots revealed that Ang II and PE each downregulate Kv4.3 mRNA and protein. However, although PE induces a faster and more extensive hypertrophic response than Ang II, the PE effect on Kv4.3 mRNA develops slowly and is sustained, whereas Ang II rapidly and transiently decreases Kv4.3 mRNA expression. Turnover measurements revealed that Kv4.3 mRNA is very stable, with a half-life >20 hours. This suggests that Ang II must destabilize the channel mRNA. In contrast, PE does not affect the rate of Kv4.3 mRNA degradation. To test for transcriptional regulation, the 5' flanking region of the rat Kv4.3 gene was cloned, and Kv4.3 promoter-reporter constructs were expressed in cardiac myocytes. Whereas Ang II was found to have no effect on transcription, PE inhibits Kv4.3 promoter activity. Pharmacological experiments also indicate that PE and Ang II act independently to downregulate Kv4.3 gene expression. Thus, regulation of Kv4.3 gene expression is not a simple secondary response to hypertrophy. Rather, Ang II and PE use different mechanisms to decrease Kv4.3 channel expression in neonatal rat cardiac myocytes.
Key Words: hypertrophy • gene regulation • ion channels/membrane transport • angiotensin-converting enzyme/angiotensin receptor • physiological and pathological control of gene expression
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