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Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/14

Title: Distribution of Kir6.0 and SUR2 ATP-sensitive potassium channel subunits in isolated ventricular myocytes
Authors: Singh, Harprit
Hudman, Diane
Lawrence, C.L.
Rainbow, Richard Daniel
Lodwick, David
Norman, Robert I.
Issue Date: May-2003
Publisher: Elsevier Science
Citation: Journal of Molecular and Cellular Cardiology 2003, 35(5), 445-449
Abstract: The subcellular distribution of ATP-sensitive potassium (KATP) channel subunits in rat-isolated ventricular myocytes was investigated using a panel of subunit-specific antisera. Kir6.1 subunits were associated predominantly with myofibril structures and were co-localized with the mitochondrial marker MitoFluor red (correlation coefficient (cc) = 0.63 ± 0.05). Anti-Kir6.1 antibodies specifically recognized a polypeptide of 48 kDa in mitochondrial membrane fractions consistent with the presence of Kir6.1 subunits in this organelle. Both Kir6.2 and SUR2A subunits were distributed universally over the sarcolemma. Lower-intensity antibody-associated immunofluorescence was detected intracellularly, which was correlated with the distribution of MitoFluor red in both cases (cc, Kir6.2, 0.56 ± 0.05; SUR2A, 0.61 ± 0.06). A polypeptide of 40 kDa was recognized by anti-Kir6.2-subunit antibodies in western blots of both microsomal and mitochondrial membrane fractions consistent with the presence of this subunit in the sarcolemma and mitochondria. Similarly, SUR2A and SUR2B subunits were detected in western blots of microsomal membrane proteins consistent with a sarcolemmal localization for these polypeptides. SUR2B subunits were shown in confocal microscopy to co-localize strongly with t-tubules (cc, 0.81 ± 0.05). Together, the results indicate that Kir6.2 and SUR2A subunits predominate in the sarcolemma of ventricular myocytes consistent with a Kir6.2/SUR2A-subunit combination in the sarcolemmal KATPchannel. Kir6.1, Kir6.2 and SUR2A subunits were demonstrated in mitochondria. Combinations of these subunits would not explain the reported pharmacology of the mitochondrial KATP channel (Mol Pharmacol 59 (2001) 225) suggesting the possibility of further unidentified components of this channel.
DOI Link: 10.1016/S0022-2828(03)00041-5
ISSN: 0022-2828
eISSN: 1095-8584
Links: http://hdl.handle.net/2381/14
http://www.sciencedirect.com/science/article&(...)
Version: Post print
Status: Peer reviewed
Type: Article
Rights: © 2003 Elsevier Science Ltd. All rights reserved. Deposited with reference to the publisher's archiving policy available on the SHERPA/RoMEO website.
Description: This is the authors' final version of the paper published in the Journal of Molecular and Cellular Cardiology
Appears in Collections:Published Articles, Dept. of Cardiovascular Sciences

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