Serum amyloid A in atherosclerosis

被引:95
作者
King, Victoria L. [2 ]
Thompson, Joel [1 ]
Tannock, Lisa R. [1 ,3 ]
机构
[1] Univ Kentucky, Div Endocrinol & Mol Med, Lexington, KY 40536 USA
[2] Univ Kentucky, Div Cardiovasc Med, Lexington, KY 40536 USA
[3] Dept Vet Affairs, Lexington, KY USA
关键词
cardiovascular disease; HDL; inflammation; obesity; proteoglycans; C-REACTIVE PROTEIN; PREMATURE CORONARY ATHEROSCLEROSIS; REVERSE CHOLESTEROL TRANSPORT; TO-RETENTION HYPOTHESIS; LIPOPROTEIN RETENTION; CARDIOVASCULAR RISK; ARTERY-DISEASE; MURINE MODELS; IN-VIVO; EXPRESSION;
D O I
10.1097/MOL.0b013e3283488c39
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose of review Serum amyloid A (SAA) is a family of acute-phase proteins which are shown to correlate with cardiovascular disease, but whether this SAA contributes causally to atherosclerosis development or reflects underlying disease or risk factors remains unclear. Recent findings SAA has been detected within atherosclerotic lesions and within adipose tissue where it is hypothesized that it may play a contributory role in disease development. In the acute-phase response SAA is synthesized by the liver and transported primarily in association with HDL. However, there is a growing literature suggesting that localized synthesis of SAA within the vasculature, or adipose tissue, may play a distinct role in disease development. Furthermore, SAA can be found in association with apoB-containing lipoproteins, in which its biological activity may be different. Summary This review will discuss recent experimental evidence supporting a causal role of SAA with atherosclerosis.
引用
收藏
页码:302 / 307
页数:6
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