AMP-Activated Protein Kinase α1 Regulates Cardiac Gap Junction Protein Connexin 43 and Electrical Remodeling Following Pressure Overload
| Title: | AMP-Activated Protein Kinase α1 Regulates Cardiac Gap Junction Protein Connexin 43 and Electrical Remodeling Following Pressure Overload |
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| Authors: | Ioana Alesutan, Jakob Voelkl, Florian Stöckigt, Sobuj Mia, Martina Feger, Uwe Primessnig, Mentor Sopjani, Carlos Munoz, Oliver Borst, Meinrad Gawaz, Burkert Pieske, Bernhard Metzler, Frank Heinzel, Jan Wilko Schrickel, Florian Lang |
| Source: | Cellular Physiology and Biochemistry, Vol 35, Iss 1, Pp 406-418 (2015) |
| Publisher Information: | Cell Physiol Biochem Press GmbH & Co KG, 2015. |
| Publication Year: | 2015 |
| Collection: | LCC:Physiology LCC:Biochemistry |
| Subject Terms: | Electrical remodeling, Conduction, Ampkα1, Cx43, Ubiquitination, Physiology, QP1-981, Biochemistry, QD415-436 |
| More Details: | Background/Aims: Adenosine 5'-monophosphate (AMP)-activated protein kinase (Ampk) modulates a wide array of cellular functions and regulates various ion channels and transporters. In failing human hearts an increased Ampkα1 activity was observed. The present study aimed to uncover the impact of Ampkα1 on cardiac electrical remodeling. Methods: Gene-targeted mice lacking functional Ampkα1 (Ampkα1-/-) and corresponding wild-type mice were exposed to pressure overload by “transverse aortic constriction” (TAC). In vivo electrophysiology was performed with a single catheter technique, myocardial conduction velocities and conduction characteristics investigated in isolated hearts, transcript levels quantified by RT-PCR and protein abundance determined by Western blotting. Moreover, connexin 43 (Cx43) was expressed in Xenopus oocytes with or without coexpression of wild-type or mutant AMPK and Cx43 protein abundance quantified utilizing confocal microscopy. Results: TAC treatment increased Ampkα1 protein expression in cardiac tissue from wild-type mice. TAC further increased left ventricular conduction inhomogeneity and triggered conduction blocks, effects blunted in the Ampkα1-/- mice. TAC treatment decreased Cx43 protein abundance in cardiac tissue, an effect significantly blunted in the Ampkα1-/- mice. TAC treatment did not modify Cx43 mRNA levels but increased ubiquitination of Cx43 protein, an effect mitigated by Ampkα1 deficiency. As shown in Xenopus oocytes, Cx43 cell membrane protein abundance was significantly downregulated by wild-type AMPKWT and constitutively active AMPKγR70Q, but not by catalytically inactive AMPKαK45R. Conclusion: Ampkα1 stimulates ubiquitination of the gap junction protein Cx43, thereby contributing to gap junction remodeling following pressure overload. |
| Document Type: | article |
| File Description: | electronic resource |
| Language: | English |
| ISSN: | 1015-8987 1421-9778 |
| Relation: | http://www.karger.com/Article/FullText/369706; https://doaj.org/toc/1015-8987; https://doaj.org/toc/1421-9778 |
| DOI: | 10.1159/000369706 |
| Access URL: | https://doaj.org/article/f6222a8ad7744751a5086b0c52b0c7f5 |
| Accession Number: | edsdoj.f6222a8ad7744751a5086b0c52b0c7f5 |
| Database: | Directory of Open Access Journals |
| ISSN: | 10158987 14219778 |
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| DOI: | 10.1159/000369706 |
| Published in: | Cellular Physiology and Biochemistry |
| Language: | English |