| Literature DB >> 29863663 |
Jui-Tung Liu1, Mary Paige Lamprecht1, Stephen A Duncan2.
Abstract
The ability to differentiate human induced pluripotent stem cells (iPSCs) into hepatocyte-like cells (HLCs) provides new opportunities to study inborn errors in hepatic metabolism. However, to provide a platform that supports the identification of small molecules that can potentially be used to treat liver disease, the procedure requires a culture format that is compatible with screening thousands of compounds. Here, we describe a protocol using completely defined culture conditions, which allow the reproducible differentiation of human iPSCs to hepatocyte-like cells in 96-well tissue culture plates. We also provide an example of using the platform to screen compounds for their ability to lower Apolipoprotein B (APOB) produced from iPSC-derived hepatocytes generated from a familial hypercholesterolemia patient. The availability of a platform that is compatible with drug discovery should allow researchers to identify novel therapeutics for diseases that affect the liver.Entities:
Mesh:
Year: 2018 PMID: 29863663 PMCID: PMC6101263 DOI: 10.3791/57194
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355