| Literature DB >> 34128205 |
Seungmi Ryu1, Pei-Hsuan Chu1, Claire Malley1, John Braisted1, Pinar Ormanoglu1, Ruili Huang1, Misha Itkin1, Zina Itkin1, Paul Shinn1, Carleen Klumpp-Thomas1, Sam Michael1, Carlos A Tristan1, Anton Simeonov1, Ilyas Singeç2.
Abstract
Human pluripotent stem cells (hPSCs), such as induced pluripotent stem cells (iPSCs), hold great promise for drug discovery, toxicology studies, and regenerative medicine. Here, we describe standardized protocols and experimental procedures that combine automated cell culture for scalable production of hPSCs with quantitative high-throughput screening (qHTS) in miniaturized 384-well plates. As a proof of principle, we established dose-response assessments and determined optimal concentrations of 12 small molecule compounds that are commonly used in the stem cell field. Multi-parametric analysis of readouts from diverse assays including cell viability, mitochondrial membrane potential, plasma membrane integrity, and ATP production was used to distinguish normal biological responses from cellular stress induced by small molecule treatment. Collectively, the establishment of integrated workflows for cell manufacturing, qHTS, high-content imaging, and data analysis provides an end-to-end platform for industrial-scale projects and should leverage the drug discovery process using hPSC-derived cell types.Entities:
Keywords: Cell viability; Dose–response curves; Embryonic stem cells; High-throughput screening; Induced pluripotent stem cells; Robotic cell culture; Small molecules; Toxicity
Mesh:
Year: 2022 PMID: 34128205 PMCID: PMC9520585 DOI: 10.1007/7651_2021_394
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745