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一种用于研究 ABCB4 转运功能的独特体外分析方法。

A Unique In Vitro Assay to Investigate ABCB4 Transport Function.

机构信息

SOLVO Biotechnology, Charles River Laboratories Hungary, H-1117 Budapest, Hungary.

Doctoral School of Molecular Medicine, Semmelweis University, Tűzoltó u. 37-47, H-1094 Budapest, Hungary.

出版信息

Int J Mol Sci. 2023 Feb 24;24(5):4459. doi: 10.3390/ijms24054459.

Abstract

ABCB4 is almost exclusively expressed in the liver, where it plays an essential role in bile formation by transporting phospholipids into the bile. ABCB4 polymorphisms and deficiencies in humans are associated with a wide spectrum of hepatobiliary disorders, attesting to its crucial physiological function. Inhibition of ABCB4 by drugs may lead to cholestasis and drug-induced liver injury (DILI), although compared with other drug transporters, there are only a few identified substrates and inhibitors of ABCB4. Since ABCB4 shares up to 76% identity and 86% similarity in the amino acid sequence with ABCB1, also known to have common drug substrates and inhibitors, we aimed to develop an ABCB4 expressing Abcb1-knockout MDCKII cell line for transcellular transport assays. This in vitro system allows the screening of ABCB4-specific drug substrates and inhibitors independently of ABCB1 activity. Abcb1KO-MDCKII-ABCB4 cells constitute a reproducible, conclusive, and easy to use assay to study drug interactions with digoxin as a substrate. Screening a set of drugs with different DILI outcomes proved that this assay is applicable to test ABCB4 inhibitory potency. Our results are consistent with prior findings concerning hepatotoxicity causality and provide new insights for identifying drugs as potential ABCB4 inhibitors and substrates.

摘要

ABCB4 几乎只在肝脏中表达,在那里它通过将磷脂转运到胆汁中在胆汁形成中发挥重要作用。人类的 ABCB4 多态性和缺乏与广泛的肝胆疾病有关,证明了它的关键生理功能。药物抑制 ABCB4 可能导致胆汁淤积和药物性肝损伤 (DILI),尽管与其他药物转运蛋白相比,只有少数已确定的 ABCB4 的底物和抑制剂。由于 ABCB4 在氨基酸序列上与 ABCB1(也已知具有共同的药物底物和抑制剂)具有高达 76%的同一性和 86%的相似性,我们旨在开发表达 Abcb1 敲除的 MDCKII 细胞系用于细胞间转运测定的 ABCB4。这种体外系统允许独立于 ABCB1 活性筛选 ABCB4 特异性药物底物和抑制剂。Abcb1KO-MDCKII-ABCB4 细胞构成了一种可重复、结论明确且易于使用的测定法,可用于研究作为底物的地高辛与药物相互作用。对一组具有不同 DILI 结果的药物进行筛选证明,该测定法适用于测试 ABCB4 的抑制效力。我们的结果与先前关于肝毒性因果关系的发现一致,并为鉴定药物作为潜在的 ABCB4 抑制剂和底物提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3544/10003010/40cd79e843dd/ijms-24-04459-g001.jpg

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