Evidence map›Paper›PMID 30457474›Full record

ArticleCell cycle (Georgetown, Tex.)2018

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

Dong Li, Jan Secher, Poul Hyttel, Marilin Ivask, Miriam Kolko, Vanessa Jane Hall, Kristine K Freude

Abstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. World journal of stem cells · 2022
    Article
  9. Article
  10. Perspectives of pluripotent stem cells in livestock.World journal of stem cells · 2021
    Review
  11. Article
  12. Review
  13. Induced pluripotent stem cells from farm animals.Journal of animal science · 2020
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Dong Lia Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences , University of Copenhagen , Frederiksberg C , Denmark.
Jan Secherb Department of Veterinary Clinical Sciences, Faculty of Health and Medical Sciences , University of Copenhagen , Taastrup , Denmark.
Poul Hyttela Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences , University of Copenhagen , Frederiksberg C , Denmark.
Marilin Ivaskc Institute of Biomedicine and Translational Medicine , University of Tartu , Tartu , Estonia.ORCID 0000-0002-3512-5052
Miriam Kolkoe Department of Drug Design and Pharmacology , University of Copenhagen , Copenhagen O , Denmark.
Vanessa Jane Halla Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences , University of Copenhagen , Frederiksberg C , Denmark.ORCID 0000-0002-3598-2214
Kristine K Freudea Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences , University of Copenhagen , Frederiksberg C , Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Cellular ReprogrammingAnimalsCell DifferentiationCells, CulturedEmbryoid BodiesFemaleFibroblastsInduced Pluripotent Stem CellsKaryotypeMiceMice, Inbred NODMice, SCIDNanog Homeobox ProteinOctamer Transcription Factor-3PlasmidsSOXB1 Transcription FactorsNanog Homeobox ProteinOctamer Transcription Factor-3SOXB1 Transcription Factorsin vitro differentiationnon-integrative strategiesPorcine induced pluripotent stem cellstransgene-free piPSCs

Identifiers

PMID30457474
PMCPMC6300098

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.