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From the Departments of Medicine (H.C.S.), Pathology (K.A.R.), and Pharmacology (M.V.B., M.J.M., H.C.S.), Duke University School of Medicine, Durham, NC.
Correspondence to Michael J. Morales, Department of Pharmacology, Box 3845, Bell Building, Room 345, Duke University Medical Center, Durham, NC 27710. E-mail mmorales{at}acpub.duke.edu
Abstract Repolarization of the cardiac action potential varies widely throughout the heart. This could be due to the differential distribution of ion channels responsible for repolarization, especially the K+ channels. We have therefore studied the cardiac localization of ERG, a channel protein known to play an important role in generation of the rapid component of the delayed rectifier K+ current (IKr), an important determinant of the repolarization waveform. Cryosections of the ferret atrium and ventricle were prepared to determine the localization of ERG by fluorescence in situ hybridization (FISH) and immunofluorescence. We found that in the ferret, ERG transcript and protein expression was most abundant in the epicardial cell layers throughout most of the ventricle, except at the base. In the atrium, we found that ERG is most abundant in the medial right atrium, especially in the trabeculae and the crista terminalis of the right atrial appendage. It also is present in areas within the sinoatrial node. In all regions studied, FISH and immunofluorescence showed concordant localization patterns. These data suggest that repolarization mediated by IKr is not uniform throughout the ferret heart and provide a molecular explanation for heterogeneity in action potential repolarization throughout the mammalian heart.
Key Words: in situ hybridization immunolocalization K+ channel ventricle atrium
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