ER Protein Quality Control and the Unfolded Protein Response in the Heart

被引:32
作者
Arrieta, A. [1 ,2 ]
Blackwood, E. A. [1 ,2 ]
Glembotski, C. C. [1 ,2 ]
机构
[1] San Diego State Univ, Inst Heart, San Diego, CA 92182 USA
[2] San Diego State Univ, Dept Biol, San Diego, CA 92182 USA
来源
COORDINATING ORGANISMAL PHYSIOLOGY THROUGH THE UNFOLDED PROTEIN RESPONSE | 2018年 / 414卷
关键词
ENDOPLASMIC-RETICULUM STRESS; CARDIAC-HYPERTROPHY; OXIDATIVE STRESS; O-GLCNAC; CALCIUM; DYSFUNCTION; ATF6; ACTIVATION; MECHANISMS; APOPTOSIS;
D O I
10.1007/82_2017_54
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cardiac myocytes are the cells responsible for the robust ability of the heart to pump blood throughout the circulatory system. Cardiac myocytes grow in response to a variety of physiological and pathological conditions; this growth challenges endoplasmic reticulum-protein quality control (ER-PQC), a major feature of which includes the unfolded protein response (UPR). ER-PQC and the UPR in cardiac myocytes growing under physiological conditions, including normal development, exercise, and pregnancy, are sufficient to support hypertrophic growth of each cardiac myocyte. However, the ER-PQC and UPR are insufficient to respond to the challenge of cardiac myocyte growth under pathological conditions, including myocardial infarction and heart failure. In part, this insufficiency is due to a continual decline in the expression levels of important adaptive UPR components as a function of age and during myocardial pathology. This chapter will discuss the physiological and pathological conditions unique to the heart that involves ER-PQC, and whether the UPR is adaptive or maladaptive under these circumstances.
引用
收藏
页码:193 / 213
页数:21
相关论文
共 93 条
  • [1] Animal Models of Myocardial and Vascular Injury
    Abarbanell, Aaron M.
    Herrmann, Jeremy L.
    Weil, Brent R.
    Wang, Yue
    Tan, Jiangning
    Moberly, Steven P.
    Fiege, Jeremy W.
    Meldrum, Daniel R.
    [J]. JOURNAL OF SURGICAL RESEARCH, 2010, 162 (02) : 239 - 249
  • [2] Determination of cell types and numbers during cardiac development in the neonatal and adult rat and mouse
    Banerjee, Indroneal
    Fuseler, John W.
    Price, Robert L.
    Borg, Thomas K.
    Baudino, Troy A.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2007, 293 (03): : H1883 - H1891
  • [3] Coordination of growth and endoplasmic reticulum stress signaling by regulator of calcineurin 1 (RCAN1), a novel ATF6-inducible gene
    Belmont, Peter J.
    Tadimalla, Archana
    Chen, Wenqiong J.
    Martindale, Joshua J.
    Thuerauf, Donna J.
    Marcinko, Marie
    Gude, Natalie
    Sussman, Mark A.
    Glembotski, Christopher C.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (20) : 14012 - 14021
  • [4] Cardiac excitation-contraction coupling
    Bers, DM
    [J]. NATURE, 2002, 415 (6868) : 198 - 205
  • [5] Calcium cycling and signaling in cardiac myocytes
    Bers, Donald M.
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 2008, 70 : 23 - 49
  • [6] Genetics of Sudden Cardiac Death
    Bezzina, Connie R.
    Lahrouchi, Najim
    Priori, Silvia G.
    [J]. CIRCULATION RESEARCH, 2015, 116 (12) : 1919 - 1936
  • [7] Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy
    Burke, Michael A.
    Cook, Stuart A.
    Seidman, Jonathan G.
    Seidman, Christine E.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2016, 68 (25) : 2871 - 2886
  • [8] Physiological myocardial hypertrophy: how and why?
    Catalucci, Daniele
    Latronico, Michael V. G.
    Ellingsen, Oyvind
    Condorelli, Gianluigi
    [J]. FRONTIERS IN BIOSCIENCE-LANDMARK, 2008, 13 : 312 - 324
  • [9] Cardiac Mitochondria and Reactive Oxygen Species Generation
    Chen, Yeong-Renn
    Zweier, Jay L.
    [J]. CIRCULATION RESEARCH, 2014, 114 (03) : 524 - 537
  • [10] Pregnancy as a cardiac stress model
    Chung, Eunhee
    Leinwand, Leslie A.
    [J]. CARDIOVASCULAR RESEARCH, 2014, 101 (04) : 561 - 570