许艳妮,高洁,徐扬,刘继开,来芳芳,巫晔翔,洪斌,司书毅. 人膜转运蛋白ABCA1表达上调剂的筛选与鉴定J. 药学学报, 2012,47(4): 446-451.
引用本文: 许艳妮,高洁,徐扬,刘继开,来芳芳,巫晔翔,洪斌,司书毅. 人膜转运蛋白ABCA1表达上调剂的筛选与鉴定J. 药学学报, 2012,47(4): 446-451.
XU Yan-Ni, GAO Jie, XU Yang, LIU Ji-Kai, LAI Fang-Fang, WU Ye-Xiang, HONG Bin, CI Shu-Yi. Screening and identification of the upregulators of ATP-binding cassette transporter A1J. 药学学报, 2012,47(4): 446-451.
Citation: XU Yan-Ni, GAO Jie, XU Yang, LIU Ji-Kai, LAI Fang-Fang, WU Ye-Xiang, HONG Bin, CI Shu-Yi. Screening and identification of the upregulators of ATP-binding cassette transporter A1J. 药学学报, 2012,47(4): 446-451.

人膜转运蛋白ABCA1表达上调剂的筛选与鉴定

Screening and identification of the upregulators of ATP-binding cassette transporter A1

  • 摘要:

    ATP结合盒转运体A1 (ATP-binding cassette transporter A1, ABCA1) 可介导细胞内磷脂和游离胆固醇转运至贫脂或无脂的载脂蛋白A-I (apolipoprotein A-I, apoA-I), 从而促进高密度脂蛋白 (high density lipoprotein, HDL) 生成, 启动胆固醇逆转运过程, 在机体清除多余脂质的过程中发挥重要作用。因此, 本研究以ABCA1为靶点, 前期建立了ABCA1上调剂抗动脉粥样硬化 (atherosclerosis, AS) 药物筛选模型, 以期寻找具有新作用机制的抗AS药物。在此研究中, 利用该模型对1 600个化合物进行筛选, 发现2030421B上调活性大于50%, EC50 0.50 µg·mL−1。进一步研究发现, 2030421B不仅能上调ABCA1mRNA以及蛋白水平, 而且能使小鼠巨噬细胞RAW264.7内胆固醇流出增加, 脂滴量减少, 是具有较好效果的ABCA1上调剂。

     

    Abstract:

    ATP-binding cassette transporter A1 (ABCA1) promotes cholesterol and phospholipid efflux from cells to lipid-poor apolipoprotein A-I (apoA-I), and plays a key role in the initial steps of the whole process of reverse cholesterol transport (RCT).  Upregulation of ABCA1 is beneficial for atherosclerosis (AS) prevention and/or therapy, which indicated that ABCA1 was a target for anti-AS drug development.  In the previous study, a high-throughput screening method was established using ABCA1p-LUC HepG2 cell line to find the upregulators of ABCA1.  In the present study, compound 2030421B was found using this method, with EC50 of 0.50 µg·mL−1.  The compound was further identified as an upregulator of ABCA1 expression by real-time quantitative reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting analysis.  Studies also showed that the 2030421B could induce apoA-I-mediated cholesterol efflux and inhibit lipids uptake into mouse peritoneal macrophages RAW264.7.

     

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