Setup and use of HepaRG cells in cholestasis research
Methods in Molecular Biology, ISSN: 1940-6029, Vol: 1981, Page: 291-312
2019
- 8Citations
- 14Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations8
- Citation Indexes8
- CrossRef2
- Captures14
- Readers14
- 14
Book Chapter Description
Since HepaRG cells can differentiate into well-polarized mature hepatocyte-like cells that synthesize, conjugate, and secrete bile acids, they represent an appropriate surrogate to primary human hepatocytes for investigations on drug-induced cholestasis mechanisms. In this chapter, culture conditions for obtaining HepaRG hepatocytes and the main methods used to detect cholestatic potential of drugs are described. Assays for evaluation of bile canaliculi dynamics and morphology are mainly based on time-lapse and phase-contrast microscopy analysis. Bile acid uptake, trafficking, and efflux are investigated using fluorescent probes. Individual bile acids are quantified in both culture media and cell layers by high-pressure liquid chromatography/tandem mass spectrometry. Preferential cellular accumulation of toxic hydrophobic bile acids is easily evidenced when exogenous primary and secondary bile acids are added to the culture medium.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85065289636&origin=inward; http://dx.doi.org/10.1007/978-1-4939-9420-5_19; http://www.ncbi.nlm.nih.gov/pubmed/31016662; http://link.springer.com/10.1007/978-1-4939-9420-5_19; https://dx.doi.org/10.1007/978-1-4939-9420-5_19; https://link.springer.com/protocol/10.1007/978-1-4939-9420-5_19
Springer Science and Business Media LLC
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