Current laboratory methods used to passage adherent human pluripotent stem cells (hPSCs) are labor intensive, result in reduced cell viability and are incompatible with larger scale production necessary for many clinical applications. To meet the current demand for hPSCs, we have developed a new non-enzymatic passaging method using sodium citrate. Sodium citrate, formulated as a hypertonic solution, gently and efficiently detaches adherent cultures of hPSCs as small multicellular aggregates with minimal manual intervention. These multicellular aggregates are easily and reproducibly recovered in calcium-containing medium, retain a high post-detachment cell viability of 97%±1% and readily attach to fresh substrates. Together, this significantly reduces the time required to expand hPSCs as high quality adherent cultures. Cells subcultured for 25 passages using this novel sodium citrate passaging solution exhibit characteristic hPSC morphology, high levels (>80%) of pluripotency markers OCT4, SSEA-4, TRA-1-60 andTRA-1-81, a normal G-banded karyotype and the ability to differentiate into cells representing all three germ layers, both in vivo and in vitro.
Scalable Passaging of Adherent Human Pluripotent Stem Cells
Ying Nie,Patrick Walsh,D. Clarke,J. Rowley,T. Fellner
Published 2014 in PLoS ONE
ABSTRACT
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- Publication year
2014
- Venue
PLoS ONE
- Publication date
2014-01-30
- Fields of study
Biology, Medicine, Materials Science
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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