Evidence map›Paper›PMID 28607560›Full record

ArticleStem cells international2017

Characterization of Mesenchymal Stem Cell-Like Cells Derived From Human iPSCs via Neural Crest Development and Their Application for Osteochondral Repair.

Ryota Chijimatsu, Makoto Ikeya, Yukihiko Yasui, Yasutoshi Ikeda, Kosuke Ebina, Yu Moriguchi, Kazunori Shimomura, David A Hart, Yoshikawa Hideki, Nakamura Norimasa

Open access · goldAbstract read
In one paragraph

Article in Stem cells international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
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

39 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
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  11. Mesodermal Derivatives of Pluripotent Stem Cells Route to Scarless Healing.International journal of molecular sciences · 2023
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Neural crest-like stem cells for tissue regeneration.Stem cells translational medicine · 2021
    Review
  19. The Progress of Stem Cell Technology for Skeletal Regeneration.International journal of molecular sciences · 2021
    Review
  20. 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

10 authors at 4 institutions in 2 countries.

Ryota ChijimatsuGraduate School of Medicine, Orthopaedic Surgery, Osaka University, Suita, Osaka, Japan.ORCID 0000-0002-3125-4818
Makoto IkeyaCenter for iPS Cell Research and Application, Life Science Frontiers, Kyota University, Kyoto, Kyoto, Japan.
Yukihiko YasuiGraduate School of Medicine, Orthopaedic Surgery, Osaka University, Suita, Osaka, Japan.
Yasutoshi IkedaGraduate School of Medicine, Orthopaedic Surgery, Osaka University, Suita, Osaka, Japan.
Kosuke EbinaGraduate School of Medicine, Orthopaedic Surgery, Osaka University, Suita, Osaka, Japan.
Yu MoriguchiGraduate School of Medicine, Orthopaedic Surgery, Osaka University, Suita, Osaka, Japan.
Kazunori ShimomuraGraduate School of Medicine, Orthopaedic Surgery, Osaka University, Suita, Osaka, Japan.
David A HartMcCaig Institute for Bone and Joint Health, University of Calgary, Calgary, Canada.ORCID 0000-0001-8580-294X
Yoshikawa HidekiGraduate School of Medicine, Orthopaedic Surgery, Osaka University, Suita, Osaka, Japan.
Nakamura NorimasaGraduate School of Medicine, Orthopaedic Surgery, Osaka University, Suita, Osaka, Japan.ORCID 0000-0001-5631-4912
The University of Osaka · JPOsaka Health Science University · JPSapporo Medical University · JPUniversity of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) derived from induced pluripotent stem cells (iPSCs) are a promising cell source for the repair of skeletal disorders. Recently, neural crest cells (NCCs) were reported to be effective for inducing mesenchymal progenitors, which have potential to differentiate into osteochondral lineages. Our aim was to investigate the feasibility of MSC-like cells originated from iPSCs via NCCs for osteochondral repair. Initially, MSC-like cells derived from iPSC-NCCs (iNCCs) were generated and characterized in vitro. These iNCC-derived MSC-like cells (iNCMSCs) exhibited a homogenous population and potential for osteochondral differentiation. No upregulation of pluripotent markers was detected during culture. Second, we implanted iNCMSC-derived tissue-engineered constructs into rat osteochondral defects without any preinduction for specific differentiation lineages. The implanted cells remained alive at the implanted site, whereas they failed to repair the defects, with only scarce development of osteochondral tissue in vivo. With regard to tumorigenesis, the implanted cells gradually disappeared and no malignant cells were detected throughout the 2-month follow-up. While this study did not show that iNCMSCs have efficacy for repair of osteochondral defects when implanted under undifferentiated conditions, iNCMSCs exhibited good chondrogenic potential in vitro under appropriate conditions. With further optimization, iNCMSCs may be a new source for tissue engineering of cartilage.

Identifiers

PMID28607560
PMCPMC5451770
OpenAlexW2615321106

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.