Published online before print October 11, 2007, doi: 10.1161/CIRCRESAHA.107.162818
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Submitted on January 16, 2007
Revised on September 26, 2007
Accepted on September 28, 2007
C-Terminal Truncation of Connexin43 Changes Number, Size, and Localization of Cardiac Gap Junction Plaques
Karen Maass ;
From the SUNY Upstate Medical University (K.M., J.S., S.E.C., M.D.), Syracuse, NY; and the Institut für Genetik (K.W.), Universita"t Bonn, Germany.
* To whom correspondence should be addressed. E-mail: delmarm{at}upstate.edu.
Haplodeficient mice expressing carboxyl-terminally truncated Cx43 (K258stop/KO), instead of the wild-type Cx43 isoform, reach adulthood and reveal no abnormalities in heart morphology. Here, we have analyzed the expression of K258stop protein and the morphology of gap junctions in adult hearts of these mice. Coimmunofluorescence analysis revealed reduced juxtaposition of K258stop with other junctional proteins at the intercalated disc. Immunoprecipitation studies documented changes in the interaction with previously described Cx43 binding proteins. Quantitative transmission electron and confocal microscopy confirmed the localization of K258stop gap junctions to the periphery of the intercalated disc and further revealed an increase in the size of K258stop gap junction plaques and a reduction in their number. Dual whole cell patch clamp analysis confirmed that K258stop gap junctions were functional, with single channel properties similar to those described in exogenous systems. We conclude that the carboxyl-terminal domain of Cx43 (Cx43CT) is involved in regulating the localization, number and size of Cx43 plaques in vivo. Conversely, protein interactions or posttranslational modifications taking place within the Cx43CT are not required for the assembly of functional gap junctions in the intercalated disc.
Key words: gap junctions • connexin43 • heart • intercalated disc
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Circ. Res. 2007 101: 1213-1215.[Extract] [Full Text] [PDF]
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