| Literature DB >> 30099335 |
Yi-Hsien Chen1, Shondra M Pruett-Miller2.
Abstract
The availability of human pluripotent stem cells (hPSCs) and progress in genome engineering technology have altered the way we approach scientific research and drug development screens. Unfortunately, the procedures for genome editing of hPSCs often subject cells to harsh conditions that compromise viability: a major problem that is compounded by the innate challenge of single-cell culture. Here we describe a generally applicable workflow that supports single-cell cloning and expansion of hPSCs after genome editing and single-cell sorting. Stem-Flex and RevitaCell supplement, in combination with Geltrex or Vitronectin (VN), promote reliable single-cell growth in a feeder-free and defined environment. Characterization of final genome-edited clones reveals that pluripotency and normal karyotype are retained following this single-cell culture protocol. This time-efficient and simplified culture method paves the way for high-throughput hPSC culture and will be valuable for both basic research and clinical applications.Entities:
Keywords: CRISPR-Cas9; Embryonic stem cells; Genome engineering; Human pluripotent stem cells; Induced pluripotent stem cells; Single-cell cloning; hESCs; hPSCs
Mesh:
Year: 2018 PMID: 30099335 DOI: 10.1016/j.scr.2018.08.003
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020