C-reactive protein in atherosclerotic lesions - Its origin and pathophysiological significance

被引:146
作者
Sun, HJ
Koike, T
Ichikawa, T
Hatakeyama, K
Shiomi, M
Zhang, B
Kitajima, S
Morimoto, M
Watanabe, T
Asada, Y
Chen, YE
Fan, JL [1 ]
机构
[1] Univ Tsukuba, Dept Pathol, Inst Basic Med Sci, Cardiovasc Dis Lab, Tsukuba, Ibaraki 3058575, Japan
[2] Miyazaki Univ, Fac Med, Dept Pathol 1, Miyazaki, Japan
[3] Kobe Univ, Sch Med, Inst Expt Anim, Kobe, Hyogo 650, Japan
[4] Fukuoka Univ, Sch Med, Dept Cardiol, Fukuoka 81401, Japan
[5] Saga Univ, Analyt Res Ctr Expt Sci, Saga 840, Japan
[6] Saga Univ, President Off, Saga 840, Japan
[7] Morehouse Sch Med, Cardiovasc Res Inst, Atlanta, GA 30310 USA
[8] Dalian Med Univ, Dept Pharmacol, Dalian, Peoples R China
关键词
D O I
10.1016/S0002-9440(10)61202-3
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
C-reactive protein (CRP) is frequently deposited in the lesions of the arterial intima; however, the origin and pathological significance of CRP in these lesions are not completely understood. in this study, we measured CRP levels in the plasma of hypercholesterolemic rabbits and investigated CRP expression at both the mRNA and protein levels using rabbit and human atherosclerotic specimens. CRP levels were significantly elevated in both cholesterol-fed and Watanabe heritable hyperlipidemic rabbits, and CRP levels were clearly correlated with aortic atherosclerotic lesion size. Immunohistochemical staining coupled with Western blotting analysis revealed that CRP-immunoreactive proteins were found at an stages of atherosclerosis from the early to advanced lesions. CRP was present extracellularly and co-localized with apolipoprotein B but was rarely associated with the cytoplasm of macrophages and foam cells. Real-time reverse transcriptase-polymerase chain reaction analysis revealed that CRP mRNA in atherosclerotic lesions was barely detectable, and isolated macrophages did not express CRP mRNA, suggesting that CRP proteins found in the lesions were essentially derived from the circulation rather than synthesized de novo by vascular cells. These results suggest that there is a link between plasma CRP and the degree of atherosclerosis and that inhibition of plasma CRP may represent a therapeutic modality for the treatment of cardiovascular disease.
引用
收藏
页码:1139 / 1148
页数:10
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