Heart failure and protein quality control

被引:177
作者
Wang, Xuejun
Robbins, Jeffrey
机构
[1] Univ S Dakota, Sanford Sch Med, Div Basic Biomed Sci, Vermillion, SD 57069 USA
[2] Childrens Hosp, Res Fdn, Cincinnati, OH 45229 USA
关键词
cardiac disease; cardiac failure; cardiac muscle; cardiomyocytes; cardiovascular disease; cardiovascular physiology;
D O I
10.1161/01.RES.0000252342.61447.a2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The heart is constantly under mechanical, metabolic, and thermal stress, even at baseline physiological conditions, and cardiac stress may increase as a result of environmental or intrinsic pathological insults. Cardiomyocytes are continuously challenged to efficiently and properly fold nascent polypeptides, traffic them to their appropriate cellular locations, and keep them from denaturing in the face of normal and pathological stimuli. Because deployment of misfolded or unfolded proteins can be disastrous, cells, in general, and cardiomyocytes, in particular, have developed a multilayered protein quality control system for maintaining proper protein conformation and for reorganizing and removing misfolded or aggregated polypeptides. Here, we examine recent data pointing to the importance of protein quality control in cardiac homeostasis and disease.
引用
收藏
页码:1315 / 1328
页数:14
相关论文
共 165 条
[11]   Increased titres of anti-human heat shock protein 60 predict an adverse one year prognosis in patients with acute cardiac chest pain [J].
Birnie, DH ;
Vickers, LE ;
Hillis, WS ;
Norrie, J ;
Cobbe, SM .
HEART, 2005, 91 (09) :1148-1153
[12]   Phosphorylation of 20S proteasome alpha subunit C8 (α7) stabilizes the 26S proteasome and plays a role in the regulation of proteasome complexes by γ-interferon [J].
Bose, S ;
Stratford, FLL ;
Broadfoot, KI ;
Mason, GGF ;
Rivett, AJ .
BIOCHEMICAL JOURNAL, 2004, 378 :177-184
[13]   Mutation R120G in αB-crystallin, which is linked to a desmin-related myopathy, results in an irregular structure and defective chaperone-like function [J].
Bova, MP ;
Yaron, O ;
Huang, QL ;
Ding, LL ;
Haley, DA ;
Stewart, PL ;
Horwitz, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (11) :6137-6142
[14]   Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation [J].
Bowman, AB ;
Yoo, SY ;
Dantuma, NP ;
Zoghbi, HY .
HUMAN MOLECULAR GENETICS, 2005, 14 (05) :679-691
[15]   Building an antibody factory: a job for the unfolded protein response [J].
Brewer, JW ;
Hendershot, LM .
NATURE IMMUNOLOGY, 2005, 6 (01) :23-29
[16]   Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases [J].
Bucciantini, M ;
Giannoni, E ;
Chiti, F ;
Baroni, F ;
Formigli, L ;
Zurdo, JS ;
Taddei, N ;
Ramponi, G ;
Dobson, CM ;
Stefani, M .
NATURE, 2002, 416 (6880) :507-511
[17]   Molecular chaperones and protein quality control [J].
Bukau, Bernd ;
Weissman, Jonathan ;
Horwich, Arthur .
CELL, 2006, 125 (03) :443-451
[18]   Age-dependent declines in proteasome activity in the heart [J].
Bulteau, AL ;
Szweda, LI ;
Friguet, B .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2002, 397 (02) :298-304
[19]   Oxidative modification and inactivation of the proteasome during coronary occlusion/reperfusion [J].
Bulteau, AL ;
Lundberg, KC ;
Humphries, KM ;
Sadek, HA ;
Szweda, PA ;
Friguet, B ;
Szweda, LI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (32) :30057-30063
[20]   Impairment of proteasome structure and function in aging [J].
Carrard, G ;
Bulteau, AL ;
Petropoulos, I ;
Friguet, B .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2002, 34 (11) :1461-1474