Adhesive Signature-based, Label-free Isolation of Human Pluripotent Stem Cells

The ability to efficiently isolate undifferentiated human induced pluripotent stem cells (UD-hiPSCs) as colonies from contaminating non-pluripotent cells is a crucial step in the stem cell field to maintain hiPSC survival, purity, and karyotype stability. Here we demonstrate significant differences...

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Veröffentlicht in:Nature methods 2013-04, Vol.10 (5), p.438-444
Hauptverfasser: Singh, Ankur, Suri, Shalu, Lee, Ted, Chilton, Jamie M., Cooke, Marissa T., Chen, Weiqiang, Fu, Jianping, Stice, Steven L., Lu, Hang, McDevitt, Todd C., García, Andrés J.
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Sprache:eng
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Zusammenfassung:The ability to efficiently isolate undifferentiated human induced pluripotent stem cells (UD-hiPSCs) as colonies from contaminating non-pluripotent cells is a crucial step in the stem cell field to maintain hiPSC survival, purity, and karyotype stability. Here we demonstrate significant differences in ‘adhesive signature’ among UD-hiPSCs, parental cells, partially reprogrammed cells, and differentiated progeny. The distinct adhesive signature of hiPSCs was exploited to rapidly (~10 min) and efficiently isolate fully reprogrammed bona fide hiPSCs as intact colonies from heterogeneous reprogramming cultures and differentiated progeny using microfluidics. hiPSCs were isolated in a label-free fashion and enriched to > 95–99% purity and survival without adversely affecting the transcriptional profile, differentiation potential or karyotype of the pluripotent cells. This rapid and label-free strategy is applicable to isolate UD-hPSCs (hiPSCs, hESCs) from heterogeneous cultures during reprogramming and routine cultures and can be expanded to purify stem cells of specific lineages, such as neurons and cardiomyocytes.
ISSN:1548-7091
1548-7105
DOI:10.1038/nmeth.2437