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载脂蛋白受体介导的 ER 输出在脂蛋白分泌和脂质稳态中的作用

Cargo Receptor-Mediated ER Export in Lipoprotein Secretion and Lipid Homeostasis.

机构信息

State Key Laboratory of Membrane Biology, Peking University, Beijing 100871, P.R. China.

Institute of Molecular Medicine, College of Future Technology, Peking University, Beijing 100871, P.R. China.

出版信息

Cold Spring Harb Perspect Biol. 2023 Jun 1;15(6):a041260. doi: 10.1101/cshperspect.a041260.

Abstract

APOB-containing lipoproteins are large, complex lipid carriers that ferry bulk lipids into the circulation via the secretory pathway, originating from the endoplasmic reticulum of specialized cells in the liver or the gut. Elevation of APOB-containing lipoproteins in the plasma represents a major risk factor for cardiovascular diseases. The production of these lipoproteins requires enzyme-catalyzed, cross-membrane transfer of neutral lipids and phospholipids to lipoproteins, in particular onto the structural component APOB. Transport of these lipid-bearing cargos relies on the COPII machinery and employs the transmembrane cargo receptor SURF4 and the small GTPase SAR1B, together constituting a selective transport program. Intriguingly, a number of factors implicated in lipoprotein production are also packaged into COPII vesicles and may be cotransported with APOB. These observations therefore point to a specialized produce-and-export itinerary during the secretion of these lipid-bearing cargos, warranting future investigations into this unique yet pivotal process at the crossroad of cell biology and physiology.

摘要

载脂蛋白 B 脂蛋白是大型复杂的脂质载体,通过分泌途径将大量脂质从肝脏或肠道的特殊细胞的内质网输送到循环系统中。血浆中载脂蛋白 B 脂蛋白的升高是心血管疾病的主要危险因素。这些脂蛋白的产生需要酶催化的、跨膜的中性脂质和磷脂向脂蛋白的转移,特别是向结构成分载脂蛋白 B 的转移。这些携带脂质的货物的运输依赖于 COPII 机制,并利用跨膜货物受体 SURF4 和小 GTP 酶 SAR1B,共同构成一个选择性的运输程序。有趣的是,一些与脂蛋白生成有关的因子也被包装到 COPII 小泡中,并可能与载脂蛋白 B 一起共运输。这些观察结果因此指出了这些携带脂质的货物分泌过程中的一种特殊的产生和输出途径,需要对这个独特但关键的细胞生物学和生理学交汇点的过程进行进一步研究。

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