Small GTPase and Regulation of Inflammation Response in Atherogenesis

被引:7
|
作者
Lu, Yuyan [1 ]
Peng, Wenhui [1 ]
Xu, Yawei [1 ]
机构
[1] Tongji Univ, Sch Med, Dept Cardiol, Shanghai Peoples Hosp 10, Shanghai 200072, Peoples R China
基金
中国国家自然科学基金;
关键词
small GTPases; inflammation; atherogenesis; cytokines; cell adhesion; cell migration; SMOOTH-MUSCLE-CELLS; ENDOTHELIAL GROWTH-FACTOR; NITRIC-OXIDE SYNTHASE; ACTIVATED PROTEIN-KINASE; SWISS; 3T3; FIBROBLASTS; LONG-TERM INHIBITION; RHO-FAMILY GTPASES; NF-KAPPA-B; CYCLOPHILIN-A; BINDING PROTEINS;
D O I
10.1097/FJC.0b013e3182a12eb3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Small GTPases are key signal transducers from extracellular stimuli to the nucleus that regulate a variety of cellular responses, including changes in gene expression and cell adhesion and migration. Accumulating data have demonstrated that abnormal activation of these small GTPases plays a critical role in the atherosclerosis characterized by vascular abnormalities, especially endothelial dysfunction and inflammation. Here, we discuss the linkage between small GTPases, inflammation, and atherogenesis. First, small GTPases affect gene expression of inflammatory cytokines through proinflammatory signaling pathways, such as nuclear factor-kappa B, vascular cell adhesion molecule-1, intercellular adhesion molecule-1, interlukin-8, and monocyte chemoattractant protein-1. Then, these molecules regulate the vascular inflammation through cell adhesion and migration. In turn, small GTPases are also regulated by extracellular stimuli, such as L-selectin, thrombin, oxidized phospholipids, and interleukins. Thus, these inflammatory cytokines generate a vicious cycle for small GTPases and inflammatory responses in the atherogenesis.
引用
收藏
页码:331 / 340
页数:10
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