Heart cells contain ATP-sensitive potassium (K(ATP)) channels in both the sarcolemma and the inner mitochondrial membrane. The sarcolemmal channels are believed to be heteromultimeric complexes of sulfonylurea receptors (SUR) and potassium inward rectifier (Kir) gene products, but the molecular identity of mitochondrial K(ATP) (mitoK(ATP)) channels remains unclear. To probe the molecular composition of K(ATP) channels, we used adenoviral gene transfer to express wild-type (WT) and dominantnegative (AFA) constructs of Kit6.1 and 6.2 in rabbit ventricular myocytes. None of the Kit6.1 or 6.2 constructs affected mitoK(ATP) channel activity as assayed by confocal imaging of flavoprotein fluorescence, contradicting the proposal, based on subcellular antibody localization, that Kir6.1 forms part of mitoK(ATP) channels. As previously reported, dominant-negative Kir6.2 gene transfer suppressed sarcolemmal K(ATP) current, while Kit6.1 constructs had no effect on sarcolemmal activity. Immunohistochemistry with an anti-Kit6.1 antibody revealed expression of this protein in heart but no apparent co-localization with mitochondria. Thus, the available evidence indicates that both Kit6.1 and 6.2 are expressed in ventricular myocytes, but neither plays a discernible functional role in the mitoK(ATP) channel. (C) 2000 Academic Press.
- Adenoviral gene transfer
- Flavoprotein fluorescence
- Mitochondrial mitoK(ATP) channel (mitoK(ATP))
- Potassium inward rectifier (Kir)
ASJC Scopus subject areas
- Molecular Biology
- Cardiology and Cardiovascular Medicine