Targeted disruption of the scavenger receptor and chemokine CXCL16 accelerates atherosclerosis

Article

关键词: LOW-DENSITY-LIPOPROTEIN;    CELL-SURFACE EXPRESSION;    E-DEFICIENT MICE;    SR-PSOX;    ENDOTHELIAL-CELLS;    HUMAN CD68;    LIGAND;    CD36;    MACROPHAGES;    REVEALS;   

DOI  :  10.1161/CIRCULATIONAHA.105.540583

来源: SCIE

【 摘 要 】

Background - The uptake of oxidized low-density lipoprotein ( OxLDL) by macrophage scavenger receptors is thought to be a key process in the formation of foam cells, the hallmark of early atherosclerotic lesions. CXCL16/scavenger receptor for phosphatidylserine and OxLDL is a multifunctional chemokine that exhibits scavenger receptor activity toward oxidized lipids in a membrane-bound configuration and may be shed to serve as a chemoattractant for T helper 1 - polarized T lymphocytes. These properties, as well as the expression of CXCL16 in human and mouse atheroma, suggest that CXCL16 plays a role in atherosclerosis. Methods and Results - To examine the role of CXCL16 in plaque formation, we created CXCL16-deficient mice ( CXCL16(-/-)) and bred them with mice deficient in the LDL receptor ( LDLR-/-). In vitro, macrophages from CXCL16(-/-) mice have a significant reduction in the capacity to bind and internalize OxLDL. We found that CXCL16(-/-)/LDLR-/- mice have accelerated atherosclerosis, enhanced macrophage recruitment to the aortic arch, and more abundant mRNA for monocyte chemotactic protein-1 and tumor necrosis factor-alpha. Conclusions - These data suggest that scavenger receptor activity mediated by CXCL16 in vivo is atheroprotective, and they contrast with studies that document protection from atherosclerosis in scavenger receptor class A - and CD36-deficient mice.

【 授权许可】

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