Original ArticleActivation of Gαq in Cardiomyocytes Increases Vps34 Activity and Stimulates AutophagyLiu, Shengnan PhD*,†; Jiang, Ya-Ping MD*; Ballou, Lisa M. PhD*; Zong, Wei-Xing PhD‡; Lin, Richard Z. MD*,§Author Information *Department of Physiology & Biophysics and Institute of Molecular Cardiology, Stony Brook University, Stony Brook, NY; †Molecular and Cellular Biology Program, Stony Brook University, Stony Brook, NY; ‡Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, NJ; and §Medical Service, Northport Veterans Affairs Medical Center, Northport, NY. Reprints: Richard Z. Lin, MD, Basic Sciences Tower 6-180, Department of Physiology & Biophysics, Stony Brook University, Stony Brook, NY 11794-8661 (e-mail: [email protected]). Supported by grants from the Department of Veterans Affairs Merit Review Program (BX002263 to R.Z.L.) and the National Institutes of Health (DK108989 to R.Z.L. and GM97355 to W.-X.Z.). The authors report no conflicts of interest. Journal of Cardiovascular Pharmacology: April 2017 - Volume 69 - Issue 4 - p 198-211 doi: 10.1097/FJC.0000000000000461 Buy Metrics Abstract Receptors that activate the heterotrimeric G protein Gαq are thought to play a role in the development of heart failure. Dysregulation of autophagy occurs in some pathological cardiac conditions including heart failure, but whether Gαq is involved in this process is unknown. We used a cardiomyocyte-specific transgenic mouse model of inducible Gαq activation (termed GαqQ209L) to address this question. After 7 days of Gαq activation, GαqQ209L hearts contained more autophagic vacuoles than wild type hearts. Increased levels of proteins involved in autophagy, especially p62 and LC3-II, were also seen. LysoTracker staining and western blotting showed that the number and size of lysosomes and lysosomal protein levels were increased in GαqQ209L hearts, indicating enhanced lysosomal degradation activity. Importantly, an autophagic flux assay measuring LC3-II turnover in isolated adult cardiomyocytes indicated that autophagic activity is enhanced in GαqQ209L hearts. GαqQ209L hearts exhibited elevated levels of the autophagy initiation complex, which contains the Class III phosphoinositide 3-kinase Vps34. As a consequence, Vps34 activity and phosphatidylinositol 3-phosphate levels were higher in GαqQ209L hearts than wild type hearts, thus accounting for the higher abundance of autophagic vacuoles. These results indicate that an increase in autophagy is an early response to Gαq activation in the heart. Copyright © 2017 Wolters Kluwer Health, Inc. All rights reserved.