脂蛋白受体在脂质转运和高脂蛋白血症发病机制中的作用。

A Chait
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摘要

存在三种不同类型的脂蛋白受体。研究得最好的是低密度脂蛋白受体,其主要功能是根据细胞需要输送胆固醇。虽然最初被认为是针对LDL的,但它清楚地识别含有载脂蛋白B或e的脂蛋白。它在LDL的分解代谢中起重要作用,也可能参与胆固醇的逆向运输。肝残体受体是肝膜上识别载脂蛋白E而不识别载脂蛋白B的独特结合位点,似乎在清除循环中的乳糜微粒(可能还有VLDL)残余物中起作用,但在识别含载脂蛋白E的HDL中也可能很重要,因此可能参与逆向胆固醇运输。最后,现在有证据表明巨噬细胞表面存在第三组脂蛋白受体。它们似乎结合了化学或生物改变的脂蛋白,可能具有清道夫的功能。虽然研究这些巨噬细胞受体的许多模型系统都集中在不太可能在体内发生的化学修饰上,但已经证明与这些受体相互作用的几种脂蛋白可能是自然产生的,或者是生物过程的结果。这三种受体的发现使我们对脂蛋白生理和病理生理的认识有了很大的提高,未来的研究应进一步扩大我们对脂蛋白代谢调控及其与高脂蛋白血症和动脉粥样硬化关系的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of lipoprotein receptors in lipid transport and in the pathogenesis of the hyperlipoproteinemias.

Three distinct classes of receptors for lipoproteins exist. The best studied is the LDL receptor, the primary function of which is the delivery of cholesterol in response to cellular needs. Although originally thought to be specific for LDL, it clearly recognizes lipoproteins that contain either apo B or E. It plays an important role in the catabolism of LDL and could also be involved in reverse cholesterol transport. The hepatic remnant receptor, a distinct binding site on liver membranes that recognizes apo E but not apo B, appears to function in the clearance of chylomicrons (and probably VLDL) remnants from the circulation, but also is likely to be important in the recognition of apo E-containing HDL, and hence is likely to participate in the reverse cholesterol transport. Finally, there is now evidence for a third group of lipoprotein receptors that are present on the cell surface of macrophages. They appear to bind lipoproteins that have been altered chemically or biologically and probably serve a scavenger function. While many of the model systems for studying these macrophage receptors have focused on chemical modifications that are unlikely to occur in vivo, several lipoproteins that have been shown to interact with these receptors may be naturally occurring or result from biological processes. The discovery of the three receptor classes has resulted in a dramatic increase in the understanding of lipoprotein physiology and pathophysiology, and future studies should further expand our understanding of the regulation of lipoprotein metabolism and its relationship to hyperlipoproteinemia and atherosclerosis.

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