Crosstalk between reverse cholesterol transport and innate immunity

被引:84
|
作者
Azzam, Kathleen M. [1 ]
Fessler, Michael B. [1 ]
机构
[1] NIEHS, Lab Resp Biol, NIH, Res Triangle Pk, NC 27709 USA
来源
基金
美国国家卫生研究院;
关键词
APOLIPOPROTEIN-A-I; PHOSPHOLIPID-TRANSFER PROTEIN; LIPOPOLYSACCHARIDE-BINDING PROTEIN; TOLL-LIKE RECEPTORS; NECROSIS-FACTOR-ALPHA; LIVER-X-RECEPTORS; LIPID RAFTS; INFLAMMATORY RESPONSE; SIGNALING PATHWAYS; MIMETIC PEPTIDE;
D O I
10.1016/j.tem.2012.02.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although lipid metabolism and host defense are widely considered to be very divergent disciplines, compelling evidence suggests that host cell handling of self- and microbe-derived (e.g. lipopolysaccharide, LPS) lipids may have common evolutionary roots, and that they indeed may be inseparable processes. The innate immune response and the homeostatic network controlling cellular sterol levels are now known to regulate each other reciprocally, with important implications for several common diseases, including atherosclerosis. In the present review we discuss recent discoveries that provide new insight into the bidirectional crosstalk between reverse cholesterol transport and innate immunity, and highlight the broader implications of these findings for the development of therapeutics.
引用
收藏
页码:169 / 178
页数:10
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