Efficient induction of transgene-free human pluripotent stem cells using a vector based on Sendai virus, an RNA virus that does not integrate into the host genome

Induced pluripotent stem cells (iPSC) have been generated from somatic cells by introducing reprogramming factors. Integration of foreign genes into the host genome is a technical hurdle for the clinical application. Here, we show that Sendai virus (SeV), an RNA virus and carries no risk of altering...

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Veröffentlicht in:Proceedings of the Japan Academy, Series B Series B, 2009, Vol.85(8), pp.348-362
Hauptverfasser: FUSAKI, Noemi, BAN, Hiroshi, NISHIYAMA, Akiyo, SAEKI, Koichi, HASEGAWA, Mamoru
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container_issue 8
container_start_page 348
container_title Proceedings of the Japan Academy, Series B
container_volume 85
creator FUSAKI, Noemi
BAN, Hiroshi
NISHIYAMA, Akiyo
SAEKI, Koichi
HASEGAWA, Mamoru
description Induced pluripotent stem cells (iPSC) have been generated from somatic cells by introducing reprogramming factors. Integration of foreign genes into the host genome is a technical hurdle for the clinical application. Here, we show that Sendai virus (SeV), an RNA virus and carries no risk of altering host genome, is an efficient solution for generating safe iPSC. Sendai-viral human iPSC expressed pluripotency genes, showed demethylation characteristic of reprogrammed cells. SeV-derived transgenes were decreased during cell division. Moreover, viruses were able to be easily removed by antibody-mediated negative selection utilizing cell surface marker HN that is expressed on SeV-infected cells. Viral-free iPSC differentiated to mature cells of the three embryonic germ layers in vivo and in vitro including beating cardiomyocytes, neurons, bone and pancreatic cells. Our data demonstrated that highly-efficient, non-integrating SeV-based vector system provides a critical solution for reprogramming somatic cells and will accelerate the clinical application. (Communicated by Kumao TOYOSHIMA, M.J.A.)
doi_str_mv 10.2183/pjab.85.348
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Jpn. Acad., Ser. B</addtitle><description>Induced pluripotent stem cells (iPSC) have been generated from somatic cells by introducing reprogramming factors. Integration of foreign genes into the host genome is a technical hurdle for the clinical application. Here, we show that Sendai virus (SeV), an RNA virus and carries no risk of altering host genome, is an efficient solution for generating safe iPSC. Sendai-viral human iPSC expressed pluripotency genes, showed demethylation characteristic of reprogrammed cells. SeV-derived transgenes were decreased during cell division. Moreover, viruses were able to be easily removed by antibody-mediated negative selection utilizing cell surface marker HN that is expressed on SeV-infected cells. Viral-free iPSC differentiated to mature cells of the three embryonic germ layers in vivo and in vitro including beating cardiomyocytes, neurons, bone and pancreatic cells. 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subjects Biomarkers - metabolism
Cell Line, Tumor
Cell Proliferation
Cellular Reprogramming - genetics
Cellular Reprogramming - physiology
DNA Methylation
Fibroblasts - metabolism
Gene Expression Profiling
Genetic Vectors - genetics
Genetic Vectors - isolation & purification
Genome, Human - genetics
human
Humans
iPS cell
Pluripotent Stem Cells - cytology
Pluripotent Stem Cells - metabolism
reprogramming
Sendai virus
Sendai virus - genetics
Sendai virus - isolation & purification
Transduction, Genetic
transgene-free
Transgenes - genetics
Virus Integration
title Efficient induction of transgene-free human pluripotent stem cells using a vector based on Sendai virus, an RNA virus that does not integrate into the host genome
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