Suppr超能文献

磷脂沉积症诱导的检测:一种高通量和高内涵形式的基于细胞的检测方法。

Detection of phospholipidosis induction: a cell-based assay in high-throughput and high-content format.

作者信息

Shahane Sampada A, Huang Ruili, Gerhold David, Baxa Ulrich, Austin Christopher P, Xia Menghang

机构信息

1National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA.

出版信息

J Biomol Screen. 2014 Jan;19(1):66-76. doi: 10.1177/1087057113502851. Epub 2013 Sep 3.

Abstract

Drug-induced phospholipidosis is characterized by the accumulation of intracellular phospholipids in cells exposed to cationic amphiphilic drugs. The appearance of unicentric or multicentric multilamellar bodies viewed under an electron microscope (EM) is the morphological hallmark of phospholipidosis. Although the EM method is the gold standard for detecting cellular phospholipidosis, this method has its drawbacks, including low throughput, high cost, and unsuitability for screening a large chemical library. In this study, a cell-based phospholipidosis assay has been developed using the LipidTOX Red reagent in HepG2 cells and miniaturized into a 1536-well plate format. To validate this assay for high-throughput screening (HTS), the LOPAC library of 1280 compounds was screened using a quantitative HTS platform. A group of known phospholipidosis inducers, such as amiodarone, propranolol, chlorpromazine, desipramine, promazine, clomipramine, and amitriptyline, was identified by the screen, consistent with previous reports. Several novel phospholipidosis inducers, including NAN-190, ebastine, GR127935, and cis-(Z)-flupentixol, were identified in this study and confirmed using the EM method. These results demonstrate that this assay can be used to evaluate and profile large numbers of chemicals for drug-induced phospholipidosis.

摘要

药物性磷脂沉积症的特征是暴露于阳离子两亲性药物的细胞内出现细胞内磷脂蓄积。在电子显微镜(EM)下观察到的单中心或多中心多层小体的出现是磷脂沉积症的形态学标志。尽管EM方法是检测细胞磷脂沉积症的金标准,但该方法存在缺点,包括通量低、成本高以及不适用于筛选大型化学文库。在本研究中,已开发出一种基于细胞的磷脂沉积症检测方法,该方法使用HepG2细胞中的LipidTOX Red试剂,并将其微型化至1536孔板形式。为了验证该检测方法用于高通量筛选(HTS)的有效性,使用定量HTS平台对1280种化合物的LOPAC文库进行了筛选。通过筛选鉴定出一组已知的磷脂沉积症诱导剂,如胺碘酮、普萘洛尔、氯丙嗪、地昔帕明、丙嗪、氯米帕明和阿米替林,这与先前的报道一致。在本研究中鉴定出几种新型磷脂沉积症诱导剂,包括NAN-190、依巴斯汀、GR127935和顺式-(Z)-氟哌噻吨,并使用EM方法进行了确认。这些结果表明,该检测方法可用于评估和分析大量化学物质的药物性磷脂沉积症。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验