Greaves David R, Gordon Siamon
Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom.
J Lipid Res. 2005 Jan;46(1):11-20. doi: 10.1194/jlr.R400011-JLR200. Epub 2004 Nov 16.
Scavenger receptors were originally defined by their ability to bind and internalize modified lipoproteins. Macrophages express at least six structurally different cell surface receptors for modified forms of LDL that contribute to foam cell formation in atherosclerosis. In addition to their role in the pathology of atherosclerosis, macrophage scavenger receptors, especially SR-A, play critical roles in innate immunity, apoptotic cell clearance, and tissue homeostasis. In this review, we highlight recent advances in understanding the biology of macrophage scavenger receptors as pattern recognition receptors for both infectious nonself (pathogens) and modified self (apoptotic cells and modified LDL). We critically evaluate the potential of scavenger receptors and their ligands as targets for therapeutic intervention in human disease.
清道夫受体最初是根据其结合和内化修饰脂蛋白的能力来定义的。巨噬细胞表达至少六种结构不同的细胞表面受体,用于识别修饰形式的低密度脂蛋白(LDL),这些受体在动脉粥样硬化中促成泡沫细胞的形成。除了在动脉粥样硬化病理学中的作用外,巨噬细胞清道夫受体,尤其是SR-A,在先天免疫、凋亡细胞清除和组织稳态中发挥关键作用。在本综述中,我们重点介绍了在理解巨噬细胞清道夫受体作为识别传染性非己(病原体)和修饰自身(凋亡细胞和修饰的LDL)的模式识别受体方面的最新进展。我们批判性地评估了清道夫受体及其配体作为人类疾病治疗干预靶点的潜力。