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Stem Cell Rev. 2013 Aug;9(4):531-6. doi: 10.1007/s12015-012-9357-8.

Standardized generation and differentiation of neural precursor cells from human pluripotent stem cells.

Author information

1
Laboratory of Molecular Biology, Division of Intramural Research, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.

Abstract

Precise, robust and scalable directed differentiation of pluripotent stem cells is an important goal with respect to disease modeling or future therapies. Using the AggreWell™400 system we have standardized the differentiation of human embryonic and induced pluripotent stem cells to a neuronal fate using defined conditions. This allows reproducibility in replicate experiments and facilitates the direct comparison of cell lines. Since the starting point for EB formation is a single cell suspension, this protocol is suitable for standard and novel methods of pluripotent stem cell culture. Moreover, an intermediate population of neural precursor cells, which are routinely >95% NCAM(pos) and Tra-1-60(neg) by FACS analysis, may be expanded and frozen prior to differentiation allowing a convenient starting point for downstream experiments.

PMID:
22388559
PMCID:
PMC3375338
DOI:
10.1007/s12015-012-9357-8
[Indexed for MEDLINE]
Free PMC Article

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