共 69 条
An oxidized lipid-peroxisome proliferator-activated receptor γ-chemokine pathway in the regulation of macrophage-vascular smooth muscle cell adhesion
被引:24
作者:

Barlic, Jana
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机构: Imperial Coll London, Fac Med, Natl Heart & Lung Inst, Leukocyte Biol Sect, London SW7 2AZ, England

Murphy, Philip M.
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h-index: 0
机构: Imperial Coll London, Fac Med, Natl Heart & Lung Inst, Leukocyte Biol Sect, London SW7 2AZ, England
机构:
[1] Imperial Coll London, Fac Med, Natl Heart & Lung Inst, Leukocyte Biol Sect, London SW7 2AZ, England
[2] NIH, NIAID, Immunol Mol Lab, Mol Signaling Sect, Bethesda, MD 20892 USA
关键词:
D O I:
10.1016/j.tcm.2007.09.004
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Recent genetic studies have implicated pro-inflammatory chemokines and chemokine receptors in atherogenesis. Studies at the molecular and cellular levels have suggested specific atherogenic mechanisms for two chemokine-chemokine receptor pairs, CCL2-CCR2 and CX3CL1-CX3CR1, involving differential receptor regulation by the transcription factor peroxisome proliferator-activated receptor gamma. This pathway is triggered by oxidized proatherogenic lipids, such as oxidized low-density lipoprotein and linoleic acid derivatives, which promote differentiation of CCR2(hi)CX3CRI(lo) human monocytes to CCR2(lo)CX3CR1(hi) macrophages that adhere to coronary artery smooth muscle cells in a CX3CR1- and peroxisome proliferator-activated receptor gamma-dependent manner. Switching CX3CR1 on and CCR2 off in vivo may result in cessation of CCR2-dependent migration and activation of CX3CR1-dependent retention that together may promote foam cell accumulation in the vessel wall.
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页码:269 / 274
页数:6
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