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高密度脂蛋白通过干扰脂筏影响抗原呈递:一种有前途的抗动脉粥样硬化策略。

High-density lipoprotein affects antigen presentation by interfering with lipid raft: a promising anti-atherogenic strategy.

机构信息

Department of Cardiology, the Second Xiangya Hospital of Central South University, Changsha, Hunan, China.

出版信息

Clin Exp Immunol. 2010 May;160(2):137-42. doi: 10.1111/j.1365-2249.2009.04068.x. Epub 2010 Jan 6.

Abstract

Atherosclerosis is a chronic inflammatory disease. Immunomodulation of atherosclerosis emerges as a promising approach to prevention and treatment of this widely prevalent disease. The function of high-density lipoprotein (HDL) to promote reverse cholesterol transport may explain the ability of its protection against atherosclerosis. Findings that HDL and apolipoprotein A-I (apoA-I) inhibited the ability of antigen presenting cells (APCs) to stimulate T cells might be attributed to lipid raft, a cholesterol-rich microdomain exhibiting functional properties depending largely upon its lipid composition. Thus, modulating cholesterol in lipid raft may provide a promising anti-atherogenic strategy.

摘要

动脉粥样硬化是一种慢性炎症性疾病。动脉粥样硬化的免疫调节作为一种广泛存在疾病的预防和治疗的有前途的方法出现了。高密度脂蛋白(HDL)促进胆固醇逆转运的功能可能解释了其对动脉粥样硬化的保护作用。发现 HDL 和载脂蛋白 A-I(apoA-I)抑制抗原呈递细胞(APC)刺激 T 细胞的能力可能归因于脂筏,这是一种富含胆固醇的微区,其功能特性在很大程度上取决于其脂质组成。因此,调节脂筏中的胆固醇可能提供一种有前途的抗动脉粥样硬化策略。

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