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β-极低密度脂蛋白对人肝实质细胞中低密度脂蛋白受体活性的完全下调作用。

Complete down-regulation of low-density lipoprotein receptor activity in human liver parenchymal cells by beta-very-low-density lipoprotein.

作者信息

Kamps J A, Kuiper J, Kruijt J K, van Berkel T J

机构信息

Division of Biopharmaceutics, Sylvius Laboratories, University of Leiden, The Netherlands.

出版信息

FEBS Lett. 1991 Aug 5;287(1-2):34-8. doi: 10.1016/0014-5793(91)80010-z.

Abstract

The effect of LDL and beta-VLDL on the expression of the LDL receptor is studied in cultured human parenchymal cells. The high affinity binding of [125I]LDL to cultured human parenchymal cells was down regulated to 37.3 +/- 2.9% and 24.0 +/- 2.6% of the control value, after preincubation with LDL or beta-VLDL for 22 h, respectively. When LDL receptor synthesis was blocked at 22 h a residual receptor activity of 29% is noticed, indicating a half-life of LDL receptors in human parenchymal cells of 12 h. It is concluded that LDL receptor expression on human liver parenchymal cells is subject to complete down-regulation by beta-VLDL, which may be held responsible for the cholesterol-rich diet induced down-regulation of LDL receptors, in vivo.

摘要

在培养的人实质细胞中研究了低密度脂蛋白(LDL)和β-极低密度脂蛋白(β-VLDL)对LDL受体表达的影响。用LDL或β-VLDL预孵育22小时后,[125I]LDL与培养的人实质细胞的高亲和力结合分别下调至对照值的37.3±2.9%和24.0±2.6%。当在22小时阻断LDL受体合成时,观察到残余受体活性为29%,表明人实质细胞中LDL受体的半衰期为12小时。结论是,人肝实质细胞上的LDL受体表达受到β-VLDL的完全下调,这可能是体内富含胆固醇饮食诱导LDL受体下调的原因。

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