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Udgivet

Generation of transgene-free porcine intermediate type induced pluripotent stem cells

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    Publikation: Bidrag til tidsskriftReviewForskningpeer review

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  3. Lactate-Mediated Protection of Retinal Ganglion Cells

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

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    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  • Dong Li
  • Jan Secher
  • Poul Hyttel
  • Marilin Ivask
  • Miriam Kolko
  • Vanessa Jane Hall
  • Kristine K Freude
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Physiologically and anatomically, humans and pigs share many similarities, which make porcine induced pluripotent stem cells (piPSCs) very attractive for modeling human cell therapy as well as for testing safety of iPSC based cell replacement therapies. To date, several integrative and non-integrative strategies have been reported to successfully generate piPSCs, but all resulting piPSCs had integration of transgenes. The use of integrative methods has the disadvantage of potential lack of silencing or inappropriate re-activation of these genes during differentiation, as well as uncertainty regarding disruption of important genomic regions caused by integration. In our study, we performed a non-integrative vector based reprogramming approach using porcine fetal fibroblasts. The resulting four piPSC lines were positive for pluripotency marker and when subjected to in vitro and in vivo differentiation assays, all four lines formed embryoid bodies, capable to differentiate into all three germ layers, and three out of the four cell lines formed teratomas. PCR analysis on genomic and plasmid DNA revealed that the episomal vectors were undetectable in six out of eight subclones derived from one of the piPSC lines (piPSC1) above passage 20. These piPSCs could potentially be ideal cell lines for the generation of porcine in vitro and in vivo models. Furthermore, subsequent analyses of our new transgene independent piPSCs could provide novel insights on the genetic and epigenetic necessities to achieve and maintain piPSCs.

OriginalsprogEngelsk
TidsskriftCell cycle (Georgetown, Tex.)
Vol/bind17
Udgave nummer23
Sider (fra-til)2547-2563
Antal sider17
ISSN1538-4101
DOI
StatusUdgivet - 2018

ID: 56579361