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载脂蛋白E介导人类单核细胞/巨噬细胞对正常极低密度脂蛋白的摄取与降解:一条不同于低密度脂蛋白受体的可饱和途径。

Apo E-mediated uptake and degradation of normal very low density lipoproteins by human monocyte/macrophages: a saturable pathway distinct from the LDL receptor.

作者信息

Wang-Iverson P, Ginsberg H N, Peteanu L A, Le N A, Brown W V

出版信息

Biochem Biophys Res Commun. 1985 Jan 16;126(1):578-86. doi: 10.1016/0006-291x(85)90645-x.

Abstract

Normal human fasting very low density lipoproteins (n-VLDL; d less than 1.006 g/ml) were demonstrated to be taken up and degraded by human monocyte-macrophages via a saturable process distinct from the previously described LDL and scavenger receptors. Through the use of apolipoprotein-phospholipid complexes, apolipoprotein E (apoE) was identified as the ligand mediating recognition of n-VLDL by this receptor.

摘要

正常人类空腹极低密度脂蛋白(n-VLDL;密度小于1.006克/毫升)经证实可被人类单核细胞-巨噬细胞通过一种不同于先前所述低密度脂蛋白和清道夫受体的可饱和过程摄取并降解。通过使用载脂蛋白-磷脂复合物,载脂蛋白E(apoE)被鉴定为介导该受体识别n-VLDL的配体。

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