Shirin Doroudgar1, Mirko Völkers1, Donna J Thuerauf1, Mohsin Khan1, Sadia Mohsin1, Jonathan L Respress1, Wei Wang1, Natalie Gude1, Oliver J Müller1, Xander H T Wehrens1, Mark A Sussman1, Christopher C Glembotski2. 1. From the San Diego State University Heart Institute and the Department of Biology, San Diego State University, CA (S.D., M.V., D.J.T., M.K., S.M., N.G., M.A.S., C.C.G.); Department of Cardiology, University of Heidelberg, Heidelberg, Germany (M.V.); DZKH (German Centre for Cardiovascular Research) Partner Site Heidelberg/Mannheim, Heidelberg, Germany (M.V.); Department of Internal Medicine III (O.J.M.), University of Heidelberg, Heidelberg, Germany; Center for Translational Medicine, Temple University School of Medicine, Philadelphia, PA (M.K., S.M.); and Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX (J.L.R., W.W., X.H.T.W.). 2. From the San Diego State University Heart Institute and the Department of Biology, San Diego State University, CA (S.D., M.V., D.J.T., M.K., S.M., N.G., M.A.S., C.C.G.); Department of Cardiology, University of Heidelberg, Heidelberg, Germany (M.V.); DZKH (German Centre for Cardiovascular Research) Partner Site Heidelberg/Mannheim, Heidelberg, Germany (M.V.); Department of Internal Medicine III (O.J.M.), University of Heidelberg, Heidelberg, Germany; Center for Translational Medicine, Temple University School of Medicine, Philadelphia, PA (M.K., S.M.); and Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX (J.L.R., W.W., X.H.T.W.). cglembotski@mail.sdsu.edu.
Abstract
RATIONALE: Hydroxymethyl glutaryl-coenzyme A reductase degradation protein 1 (Hrd1) is an endoplasmic reticulum (ER)-transmembrane E3 ubiquitin ligase that has been studied in yeast, where it contributes to ER protein quality control by ER-associated degradation (ERAD) of misfolded proteins that accumulate during ER stress. Neither Hrd1 nor ERAD has been studied in the heart, or in cardiac myocytes, where protein quality control is critical for proper heart function. OBJECTIVE: The objective of this study were to elucidate roles for Hrd1 in ER stress, ERAD, and viability in cultured cardiac myocytes and in the mouse heart, in vivo. METHODS AND RESULTS: The effects of small interfering RNA-mediated Hrd1 knockdown were examined in cultured neonatal rat ventricular myocytes. The effects of adeno-associated virus-mediated Hrd1 knockdown and overexpression were examined in the hearts of mice subjected to pressure overload-induced pathological cardiac hypertrophy, which challenges protein-folding capacity. In cardiac myocytes, the ER stressors, thapsigargin and tunicamycin increased ERAD, as well as adaptive ER stress proteins, and minimally affected cell death. However, when Hrd1 was knocked down, thapsigargin and tunicamycin dramatically decreased ERAD, while increasing maladaptive ER stress proteins and cell death. In vivo, Hrd1 knockdown exacerbated cardiac dysfunction and increased apoptosis and cardiac hypertrophy, whereas Hrd1 overexpression preserved cardiac function and decreased apoptosis and attenuated cardiac hypertrophy in the hearts of mice subjected to pressure overload. CONCLUSIONS: Hrd1 and ERAD are essential components of the adaptive ER stress response in cardiac myocytes. Hrd1 contributes to preserving heart structure and function in a mouse model of pathological cardiac hypertrophy.
RATIONALE: Hydroxymethyl glutaryl-coenzyme A reductase degradation protein 1 (Hrd1) is an endoplasmic reticulum (ER)-transmembrane E3 ubiquitin ligase that has been studied in yeast, where it contributes to ER protein quality control by ER-associated degradation (ERAD) of misfolded proteins that accumulate during ER stress. Neither Hrd1 nor ERAD has been studied in the heart, or in cardiac myocytes, where protein quality control is critical for proper heart function. OBJECTIVE: The objective of this study were to elucidate roles for Hrd1 in ER stress, ERAD, and viability in cultured cardiac myocytes and in the mouse heart, in vivo. METHODS AND RESULTS: The effects of small interfering RNA-mediated Hrd1 knockdown were examined in cultured neonatal rat ventricular myocytes. The effects of adeno-associated virus-mediated Hrd1 knockdown and overexpression were examined in the hearts of mice subjected to pressure overload-induced pathological cardiac hypertrophy, which challenges protein-folding capacity. In cardiac myocytes, the ER stressors, thapsigargin and tunicamycin increased ERAD, as well as adaptive ER stress proteins, and minimally affected cell death. However, when Hrd1 was knocked down, thapsigargin and tunicamycin dramatically decreased ERAD, while increasing maladaptive ER stress proteins and cell death. In vivo, Hrd1 knockdown exacerbated cardiac dysfunction and increased apoptosis and cardiac hypertrophy, whereas Hrd1 overexpression preserved cardiac function and decreased apoptosis and attenuated cardiac hypertrophy in the hearts of mice subjected to pressure overload. CONCLUSIONS:Hrd1 and ERAD are essential components of the adaptive ER stress response in cardiac myocytes. Hrd1 contributes to preserving heart structure and function in a mouse model of pathological cardiac hypertrophy.
Authors: Wolfgang Boecker; Oliver Y Bernecker; Joseph C Wu; Xinsheng Zhu; Tomohiro Sawa; Luanda Grazette; Anthony Rosenzweig; Federica del Monte; Ulrich Schmidt; Roger J Hajjar Journal: Mol Imaging Date: 2004-04 Impact factor: 4.488
Authors: R G Gardner; G M Swarbrick; N W Bays; S R Cronin; S Wilhovsky; L Seelig; C Kim; R Y Hampton Journal: J Cell Biol Date: 2000-10-02 Impact factor: 10.539
Authors: Adrian Arrieta; Erik A Blackwood; Winston T Stauffer; Michelle Santo Domingo; Alina S Bilal; Donna J Thuerauf; Amber N Pentoney; Cathrine Aivati; Anup V Sarakki; Shirin Doroudgar; Christopher C Glembotski Journal: J Biol Chem Date: 2020-04-23 Impact factor: 5.157