| Literature DB >> 30656621 |
Yu Chen1, Carlos A Tristan1, Sunil K Mallanna1, Pinar Ormanoglu1, Steven Titus1, Anton Simeonov1, Ilyas Singeç2.
Abstract
Human pluripotent stem cells (hPSCs) are characterized by their ability to self-renew and differentiate into any cell type of the human body. To fully utilize the potential of hPSCs for translational research and clinical applications, it is critical to develop rigorous cell differentiation protocols under feeder-free conditions that are efficient, reproducible, and scalable for high-throughput projects. Focusing on neural conversion of hPSCs, here we describe robust small molecule-based procedures that generate neural stem cells (NSCs) in less than a week under chemically defined conditions. These protocols can be used to dissect the mechanisms of neural lineage entry and to further develop systematic protocols that produce the cellular diversity of the central nervous system at industrial scale.Entities:
Keywords: Cell differentiation; Coating substrate; Culture medium; Embryonic stem cell; Induced pluripotent stem cell; Neural induction; Pathway inhibition; Pluripotency; Small molecules
Mesh:
Substances:
Year: 2019 PMID: 30656621 PMCID: PMC6908303 DOI: 10.1007/978-1-4939-9007-8_5
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745