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载脂蛋白 E 的新功能:上调 ATP 结合盒转运蛋白 A1 的表达。

A novel function of apolipoprotein E: upregulation of ATP-binding cassette transporter A1 expression.

机构信息

Department of Physiology, Wuhan University School of Basic Medical Science, Wuhan, People's Republic of China.

出版信息

PLoS One. 2011;6(7):e21453. doi: 10.1371/journal.pone.0021453. Epub 2011 Jul 11.

Abstract

Despite the well known importance of apolipoprotein (Apo) E in cholesterol efflux, the effect of ApoE on the expression of ATP-binding cassette transporter A1 (ABCA1) has never been investigated. The objective of this study was to determine the effect of ApoE on ApoB-carrying lipoprotein-induced expression of ABCA1, a protein that mediates cholesterol efflux. Our data demonstrate that ApoB-carrying lipoproteins obtained from both wild-type and ApoE knockout mice induced ApoAI-mediated cholesterol efflux in mouse macrophages, which was associated with an enhanced ABCA1 promoter activity, and an increased ABCA1 mRNA and protein expression. In addition, these lipoproteins increased the level of phosphorylated specificity protein 1 (Sp1) and the amount of Sp1 bound to the ABCA1 promoter. However, all these inductions were significantly diminished in cells treated with ApoE-free lipoproteins, when compared to those treated with wild-type lipoproteins. Enrichment with human ApoE3 reversed the reduced inducibility of ApoE-free lipoproteins. Moreover, we observed that inhibition of Sp1 DNA-binding by mithramycin A diminished ABCA1 expression and ApoAI-mediated cholesterol efflux induced by ApoB-carrying lipoproteins, and that mutation of the Sp1-binding motif in the ABCA1 promoter region diminished ApoB-carrying lipoprotein-induced ABCA1 promoter activity. Collectively, these data suggest that ApoE associated with ApoB-carrying lipoproteins has an upregulatory role on ABCA1 expression, and that induction of Sp1 phosphorylation is a mechanism by which ApoE upregulates ABCA1 expression.

摘要

尽管载脂蛋白(Apo)E 在胆固醇外排中具有重要作用,但 ApoE 对 ATP 结合盒转运体 A1(ABCA1)表达的影响从未被研究过。本研究的目的是确定 ApoE 对载脂蛋白 B 携带脂蛋白诱导的 ABCA1 表达的影响,ABCA1 是一种介导胆固醇外排的蛋白质。我们的数据表明,来自野生型和 ApoE 敲除小鼠的载脂蛋白 B 携带脂蛋白诱导了载脂蛋白 AI 介导的胆固醇外排,这与 ABCA1 启动子活性增强以及 ABCA1 mRNA 和蛋白表达增加有关。此外,这些脂蛋白增加了磷酸化特异性蛋白 1(Sp1)的水平和 Sp1 与 ABCA1 启动子结合的量。然而,与用野生型脂蛋白处理的细胞相比,在用不含 ApoE 的脂蛋白处理的细胞中,所有这些诱导作用都显著降低。用人类 ApoE3 进行富集可逆转不含 ApoE 的脂蛋白的降低诱导能力。此外,我们观察到,用米托霉素 A 抑制 Sp1 DNA 结合可减少载脂蛋白 B 携带的脂蛋白诱导的 ABCA1 表达和载脂蛋白 AI 介导的胆固醇外排,并且 ABCA1 启动子区域中的 Sp1 结合基序的突变可减少载脂蛋白 B 携带的脂蛋白诱导的 ABCA1 启动子活性。总之,这些数据表明,与载脂蛋白 B 携带的脂蛋白结合的 ApoE 对 ABCA1 表达具有上调作用,并且 Sp1 磷酸化的诱导是 ApoE 上调 ABCA1 表达的一种机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e8a/3136925/c14de8ba00d8/pone.0021453.g001.jpg

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