Cardiac remodeling in Gαq and Gα11 knockout mice.

Although both Gαq- and Gα11-protein signaling are believed to be involved in the regulation of cardiac hypertrophy, their detailed contribution to myocardial function remains elusive. We studied remodeling processes in healthy transgenic mice with genetically altered Gαq/Gα11-expression, in particular a global Gα11-knockout and a novel inducible cardiac specific Gαq-knockout, as well as a combined double knockout (dKO) mouse line. Echocardiography and telemetric ECG recordings revealed that compared with wild type mice, hearts of dKO mice showed an increased ejection fraction and a decreased heart rate, irrespective of age resulting in a maintained cardiac output. We attributed these findings to the lack of Gα11, which the absence was associated with a decreased afterload. Histological analysis of the extracellular matrix in the heart depicted a diminished presence of collagen in aging hearts of dKO mice compared to wild-type mice. The results of a transcriptome analysis on isolated ventricular cardiac myocytes revealed alterations of the activity of genes involved in the Gαq/Gα11-dependent regulation of the extracellular matrix, such as the matricellular protein Cyr61. From our data we conclude that Gαq/Gα11 signaling pathways play a pivotal role in maintaining gene activity patterns. For the heart we revealed their importance in modulating the properties of the extracellular matrix, a mechanism that might be an important contributor and mechanistic basis for the development of pressure-overload induced cardiac hypertrophy. Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Citation

Kathrina Wiesen, Elisabeth Kaiser, Laura Schröder, Anke Scholz, Sandra Ruppenthal, Jan-Christian Reil, Christina Backes, Eckart Meese, Carola Meier, Anna Bogdanova, Peter Lipp, Lars Kaestner. Cardiac remodeling in Gαq and Gα11 knockout mice. International journal of cardiology. 2016 Jan 1;202:836-45

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PMID: 26476043

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