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A Unique In Vitro Assay to Investigate ABCB4 Transport Function.
Temesszentandrási-Ambrus, Csilla; Nagy, Gábor; Bui, Annamária; Gáborik, Zsuzsanna.
Afiliación
  • Temesszentandrási-Ambrus C; SOLVO Biotechnology, Charles River Laboratories Hungary, H-1117 Budapest, Hungary.
  • Nagy G; Doctoral School of Molecular Medicine, Semmelweis University, Tuzoltó u. 37-47, H-1094 Budapest, Hungary.
  • Bui A; SOLVO Biotechnology, Charles River Laboratories Hungary, H-1117 Budapest, Hungary.
  • Gáborik Z; SOLVO Biotechnology, Charles River Laboratories Hungary, H-1117 Budapest, Hungary.
Int J Mol Sci ; 24(5)2023 Feb 24.
Article en En | MEDLINE | ID: mdl-36901890
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Colestasis / Enfermedad Hepática Inducida por Sustancias y Drogas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article País de afiliación: Hungria

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Colestasis / Enfermedad Hepática Inducida por Sustancias y Drogas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article País de afiliación: Hungria