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Generation of Human Induced Pluripotent Stem Cells Using Genome Integrating or Non-integrating Methods

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ŠIMARA Pavel TESAŘOVÁ Lenka PAĎOUROVÁ Stanislava KRONTORÁD KOUTNÁ Irena

Rok publikování 2014
Druh Článek v odborném periodiku
Časopis / Zdroj Folia Biologica
Fakulta / Pracoviště MU

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Citace
Obor Genetika a molekulární biologie
Klíčová slova hiPSCs; lentivirus; Sendai virus; episomal reprogramming
Popis Preclinical studies have demonstrated the promising potential of human induced pluripotent stem cells (hiPSCs) for clinical application. To fulfil this goal, efficient and safe methods to generate them must be established. Various reprogramming techniques were presented during seven years of hiPSCs research. Genome non-integrating and completely xeno-free protocols from the first biopsy to stable hiPSC clones are highly preferable in terms of future clinical application. In this commentary article, we summarize the reprogramming experiments performed in our laboratories. We successfully generated hiPSCs using STEMCCA lentivirus, Sendai virus or episomal vectors. Human neonatal fibroblasts and CD34+ blood progenitors were used as cell sources and were maintained either on mouse embryonic feeder cells or in feeder-free conditions. The reprogramming efficiency was comparable for all three methods and both cell types, while the best results were obtained in feeder-free conditions.
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