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Generation of integration-free induced hepatocyte-like cells from mouse fibroblasts.


ABSTRACT: The ability to generate integration-free induced hepatocyte-like cells (iHeps) from somatic fibroblasts has the potential to advance their clinical application. Here, we have generated integration-free, functional, and expandable iHeps from mouse somatic fibroblasts. To elicit this direct conversion, we took advantage of an oriP/EBNA1-based episomal system to deliver a set of transcription factors, Gata4, Hnf1a, and Foxa3, to the fibroblasts. The established iHeps exhibit similar morphology, marker expression, and functional properties to primary hepatocytes. Furthermore, integration-free iHeps prolong the survival of fumarylacetoacetate-hydrolase-deficient (Fah(-/-)) mice after cell transplantation. Our study provides a novel concept for generating functional and expandable iHeps using a non-viral, non-integrating, plasmid-based system that could facilitate their pharmaceutical and biomedical application.

SUBMITTER: Kim J 

PROVIDER: S-EPMC4621602 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Generation of integration-free induced hepatocyte-like cells from mouse fibroblasts.

Kim Jonghun J   Kim Kee-Pyo KP   Lim Kyung Tae KT   Lee Seung Chan SC   Yoon Juyong J   Song Guangqi G   Hwang Seon In SI   Schöler Hans R HR   Cantz Tobias T   Han Dong Wook DW  

Scientific reports 20151027


The ability to generate integration-free induced hepatocyte-like cells (iHeps) from somatic fibroblasts has the potential to advance their clinical application. Here, we have generated integration-free, functional, and expandable iHeps from mouse somatic fibroblasts. To elicit this direct conversion, we took advantage of an oriP/EBNA1-based episomal system to deliver a set of transcription factors, Gata4, Hnf1a, and Foxa3, to the fibroblasts. The established iHeps exhibit similar morphology, mar  ...[more]

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