Proteotoxic stress and circulating cell stress proteins in the cardiovascular diseases

被引:28
作者
Henderson, Brian [1 ]
Pockley, A. Graham [2 ]
机构
[1] UCL, UCL Eastman Dent Inst, Dept Microbial Dis, London WC1X 8LD, England
[2] Univ Sheffield, Sch Med, Dept Oncol, Sheffield, S Yorkshire, England
关键词
Cardiovascular disease; Molecular chaperone; Protein-folding catalyst; Circulating cell stress proteins; Inflammation; HEAT-SHOCK-PROTEIN; MIGRATION INHIBITORY FACTOR; CARDIAC MYOCYTES; ISCHEMIC-INJURY; CONFERS PROTECTION; SECRETORY PATHWAY; AORTIC-ANEURYSMS; OXIDATIVE STRESS; IMMUNE-SYSTEM; DANGER;
D O I
10.1007/s12192-011-0318-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The cardiovasculature is one of the major body systems and probably the one most exposed to stress. There is clear evidence that increasing levels of cell stress proteins within the heart is cardioprotective. In addition, there is rapidly emerging evidence that secreted cell stress proteins play a role in the function of the cardiovascular tissues. Those secreted proteins have three potential functions: (1) as normal homeostatic cardiovascular signals (e.g. protein disulphide isomerase); (2) as anti-inflammatory molecules, which are able to inhibit cardiovascular pathology (e.g. Hsp27); and (iii) as pro-inflammatory signals that can induce and promote cardiovascular pathology (e.g. Hsp60). As all of these various proteins may be released-at different rates-and in different cardiovascular diseases-we need to consider the cohort of potential secreted cell stress proteins as a dynamic system (network) that can aid and/or damage the equally dynamic cardiovascular system.
引用
收藏
页码:303 / 311
页数:9
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