piggyBac transposition reprograms fibroblasts to induced pluripotent stem cells (original) (raw)
- Letter
- Published: 01 March 2009
- Iacovos P. Michael1,2,
- Paria Mohseni1,2,
- Ridham Desai1,2,
- Maria Mileikovsky1,
- Riikka Hämäläinen1,
- Rebecca Cowling1,
- Wei Wang3,
- Pentao Liu3,
- Marina Gertsenstein1,
- Keisuke Kaji4,
- Hoon-Ki Sung1 &
- …
- Andras Nagy1,2
Nature volume 458, pages 766–770 (2009)Cite this article
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Abstract
Transgenic expression of just four defined transcription factors (c-Myc, Klf4, Oct4 and Sox2) is sufficient to reprogram somatic cells to a pluripotent state1,2,3,4. The resulting induced pluripotent stem (iPS) cells resemble embryonic stem cells in their properties and potential to differentiate into a spectrum of adult cell types. Current reprogramming strategies involve retroviral1, lentiviral5, adenoviral6 and plasmid7 transfection to deliver reprogramming factor transgenes. Although the latter two methods are transient and minimize the potential for insertion mutagenesis, they are currently limited by diminished reprogramming efficiencies. piggyBac (PB) transposition is host-factor independent, and has recently been demonstrated to be functional in various human and mouse cell lines8,9,10,11. The PB transposon/transposase system requires only the inverted terminal repeats flanking a transgene and transient expression of the transposase enzyme to catalyse insertion or excision events12. Here we demonstrate successful and efficient reprogramming of murine and human embryonic fibroblasts using doxycycline-inducible transcription factors delivered by PB transposition13. Stable iPS cells thus generated express characteristic pluripotency markers and succeed in a series of rigorous differentiation assays. By taking advantage of the natural propensity of the PB system for seamless excision12, we show that the individual PB insertions can be removed from established iPS cell lines, providing an invaluable tool for discovery. In addition, we have demonstrated the traceless removal of reprogramming factors joined with viral 2A sequences14 delivered by a single transposon from murine iPS lines. We anticipate that the unique properties of this virus-independent simplification of iPS cell production will accelerate this field further towards full exploration of the reprogramming process and future cell-based therapies.
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Acknowledgements
We thank J. Moffat for time-lapse image acquisition, P.-A. Pentilla for cell sorting, M.-S. Eiymo for assisting with initial PB test vector construction, J. Ure and M. Kownacka for technical assistance, M. Kibschull for establishing human embryonic fibroblasts, A. Cheung for discussions, and K. Vintersten for critical reading of the manuscript. This work was supported by the Wellcome Trust to P.L., and grants awarded to A.N. from the Canadian Stem Cell Network and JDRF.
Author Contributions K.W. designed the experiments, cloned the transposon vectors, isolated and transfected fibroblasts, cultured mouse PB-iPS lines, performed alkaline phosphatase, LacZ and immunostaining, FACS analysis, dissected embryos, prepared DNA and performed Southern blotting, collected, analysed and interpreted data, and wrote the manuscript. I.P.M. designed experiments and assisted with initial cloning. P.M. and R.D. isolated fibroblasts, and assisted with cell culture, immunostaining and embryo dissections. M.M. transfected human fibroblasts, cultured human PB-iPS lines, performed alkaline phosphatase staining, immunostaining and differentiation assays. R.H. and K.W. performed the single transposon reprogramming studies and the removal of factors from iPS cells. R.C. carried out RT–PCR reactions. W.W. and P.L. provided the PB-PGK-neo-bpA and pCyL43 transposase plasmids, and guidelines for their use. M.G. generated and coordinated the iPSC chimaera production. K.K. performed immunostaining on induced secondary fibroblasts. H.-K.S. and I.P.M. performed teratoma assays and collected microscopy images. A.N. was responsible for the project concept, supervised the experiment design and data interpretation, and wrote the manuscript. All authors were involved in initial project design, discussed the results and contributed to the manuscript preparation.
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Authors and Affiliations
- Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario M5G 1X5, Canada ,
Knut Woltjen, Iacovos P. Michael, Paria Mohseni, Ridham Desai, Maria Mileikovsky, Riikka Hämäläinen, Rebecca Cowling, Marina Gertsenstein, Hoon-Ki Sung & Andras Nagy - Department of Molecular Genetics, University of Toronto, Toronto M5S 1A8, Canada
Iacovos P. Michael, Paria Mohseni, Ridham Desai & Andras Nagy - The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK ,
Wei Wang & Pentao Liu - MRC Centre for Regenerative Medicine, Institute for Stem Cell Research, University of Edinburgh, Edinburgh EH9 3JQ, UK
Keisuke Kaji
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Supplementary Information
This file contains Supplementary Figures S1-S11 with Legends, a Supplementary Reference and Supplementary Tables 1-2 (PDF 2962 kb)
Supplementary Movie 1
This Movie shows 2o fibroblast with dox inducible reprogramming factors. (MOV 15149 kb)
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Woltjen, K., Michael, I., Mohseni, P. et al. piggyBac transposition reprograms fibroblasts to induced pluripotent stem cells.Nature 458, 766–770 (2009). https://doi.org/10.1038/nature07863
- Received: 06 November 2008
- Accepted: 12 February 2009
- Published: 01 March 2009
- Issue Date: 09 April 2009
- DOI: https://doi.org/10.1038/nature07863
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Editorial Summary
Virus-free iPS cells
The discovery that non-germline adult cells can be reprogrammed to become pluripotent, able to differentiate into any cell type, opened up exciting possibilities. Reprogrammed cells — called induced pluripotent stem (iPS) cells — should have great potential in regenerative medicine, but most current methods of producing them involve viral gene delivery that could cause abnormalities in the induced cells. Two groups in this issue report on a collaboration that has succeeded in producing pluripotency in human cells without using viral vectors. Stable iPS cells were produced in both human and mouse fibroblasts using virus-derived 2A peptide sequences to create a multicistronic vector incorporating the reprogramming factors, delivered to the cell by the piggyBac transposon vector. The 2A-linked reprogramming factors, not required in the established iPS cell lines, were then removed.