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Advanced feeder-free generation of induced pluripotent stem cells directly from blood cells.


ABSTRACT: Generation of validated human induced pluripotent stem cells (iPSCs) for biobanking is essential for exploring the full potential of iPSCs in disease modeling and drug discovery. Peripheral blood mononuclear cells (PBMCs) are attractive targets for reprogramming, because blood is collected by a routine clinical procedure and is a commonly stored material in biobanks. Generation of iPSCs from blood cells has previously been reported using integrative retroviruses, episomal Sendai viruses, and DNA plasmids. However, most of the published protocols require expansion and/or activation of a specific cell population from PBMCs. We have recently collected a PBMC cohort from the Finnish population containing more than 2,000 subjects. Here we report efficient generation of iPSCs directly from PBMCs in feeder-free conditions in approximately 2 weeks. The produced iPSC clones are pluripotent and transgene-free. Together, these properties make this novel method a powerful tool for large-scale reprogramming of PBMCs and for iPSC biobanking.

SUBMITTER: Trokovic R 

PROVIDER: S-EPMC4250212 | biostudies-literature | 2014 Dec

REPOSITORIES: biostudies-literature

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Advanced feeder-free generation of induced pluripotent stem cells directly from blood cells.

Trokovic Ras R   Weltner Jere J   Nishimura Ken K   Ohtaka Manami M   Nakanishi Mahito M   Salomaa Veikko V   Jalanko Anu A   Otonkoski Timo T   Kyttälä Aija A  

Stem cells translational medicine 20141029 12


Generation of validated human induced pluripotent stem cells (iPSCs) for biobanking is essential for exploring the full potential of iPSCs in disease modeling and drug discovery. Peripheral blood mononuclear cells (PBMCs) are attractive targets for reprogramming, because blood is collected by a routine clinical procedure and is a commonly stored material in biobanks. Generation of iPSCs from blood cells has previously been reported using integrative retroviruses, episomal Sendai viruses, and DNA  ...[more]

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