Crosstalk between macrophages and smooth muscle cells in atherosclerotic vascular diseases

被引:48
作者
Koga, Jun-ichiro [1 ]
Aikawa, Masanori [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Ctr Excellence Vasc Biol, Brigham & Womens Hosp, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Ctr Interdisciplinary Cardiovasc Sci, Brigham & Womens Hosp, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Macrophages; Smooth muscle cells; Atherosclerosis; MONOCYTE CHEMOATTRACTANT PROTEIN-1; HEAVY-CHAIN ISOFORMS; ADIPOSE-TISSUE; COLLAGEN ACCUMULATION; NEOINTIMAL FORMATION; RABBIT ATHEROMA; BALLOON-INJURY; GROWTH-FACTOR; INFLAMMATION; PLAQUES;
D O I
10.1016/j.vph.2012.02.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Macrophages and smooth muscle cells (SMCs) represent major players in the pathogenesis of atherosclerotic vascular diseases. SMCs often reside in close proximity to macrophage clusters. Activated macrophages may promote pro-atherogenic functions of SMCs. Addressing macrophage-dependent mechanisms of SMC activation may provide new insight into atherogenesis and new therapies for various vascular diseases. Direct evidence for such interplay between atherosclerosis-associated cell types, however, remains scant. While SMC-derived macrophage foam cells have long been reported, recent evidence has also identified SMC-like cells of monocyte origin, suggesting dynamic interchangeability of these cell types. Future efforts may help to understand the interplay between key cell types and offer new paradigms in vascular medicine and pharmacology. (C) 2012 Published by Elsevier Inc.
引用
收藏
页码:24 / 28
页数:5
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