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鉴定去氢依泊汀 A 为三磷酸腺苷结合盒转运体 A1(ABCA1)的新型上调调节剂。

Identification of dehydroxytrichostatin A as a novel up-regulator of the ATP-binding cassette transporter A1 (ABCA1).

机构信息

Institute of Medicinal Biotechnology, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100050, China.

出版信息

Molecules. 2011 Aug 25;16(9):7183-98. doi: 10.3390/molecules16097183.

Abstract

The ATP-binding cassette transporter A1 (ABCA1) mediates the cellular efflux of excess cholesterol and phospholipids to lipid-poor apolipoprotein A-I (apoA-I). ABCA1 plays an important role in high-density lipoprotein (HDL) biogenesis and reverse cholesterol transport. By using a cell-based screening model for the ABCA1 up-regulator and column chromatography, an active compound, 9179B, was isolated. Through analysis of its NMR data, 9179B was identified as dehydroxytrichostatin A. We found that 9179B increased the transcription of ABCA1 in a cell-based reporter assay, with an EC(50) value of 2.65 μM. 9179B up-regulated ABCA1 expression at both mRNA and protein levels in HepG2 and RAW264.7 cells. It also up-regulated the expression of scavenger receptor class B type I (SR-BI) as well as the uptake of DiI-HDL in RAW264.7 cells. This compound stimulated ApoA-I-mediated cellular cholesterol efflux from RAW 264.7 cells. We further found that 9179B was a potent histone deacetylase (HDAC) inhibitor with an IC(50) value of 0.08 μM. Reporter gene assays showed that the regulation of ABCA1 transcription by 9179B was mainly mediated by the -171/-75 bp promoter region. Together, our results indicate that 9179B is an ABCA1 up-regulator and dehydroxytrichostatin A may be a novel anti-atherogenic compound.

摘要

三磷酸腺苷结合盒转运体 A1(ABCA1)介导细胞内多余胆固醇和磷脂向脂少的载脂蛋白 A-I(apoA-I)的外排。ABCA1 在高密度脂蛋白(HDL)的生物合成和胆固醇逆向转运中发挥着重要作用。我们使用 ABCA1 上调剂的基于细胞的筛选模型和柱层析法,分离出一种活性化合物 9179B。通过分析其 NMR 数据,确定 9179B 为去羟基曲古抑菌素 A。我们发现 9179B 在基于细胞的报告基因测定中增加了 ABCA1 的转录,其 EC50 值为 2.65 μM。9179B 在 HepG2 和 RAW264.7 细胞中均能上调 ABCA1 的表达,无论是在 mRNA 还是在蛋白水平。它还上调了 RAW264.7 细胞中清道夫受体 B 型 I(SR-BI)的表达和 DiI-HDL 的摄取。该化合物刺激 RAW 264.7 细胞中 ApoA-I 介导的细胞胆固醇外排。我们进一步发现 9179B 是一种有效的组蛋白去乙酰化酶(HDAC)抑制剂,其 IC50 值为 0.08 μM。报告基因检测表明,9179B 对 ABCA1 转录的调节主要通过-171/-75 bp 启动子区域介导。总之,我们的研究结果表明 9179B 是一种 ABCA1 上调剂,而去羟基曲古抑菌素 A 可能是一种新型抗动脉粥样硬化化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4691/6264683/11ea4949acd3/molecules-16-07183-g001.jpg

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