Evidence map›Paper›PMID 25396711›Full record

ArticleTissue engineering. Part A2015

Repair mechanism of osteochondral defect promoted by bioengineered chondrocyte sheet.

Ryo Shimizu, Naosuke Kamei, Nobuo Adachi, Michio Hamanishi, Goki Kamei, Elhussein Elbadry Mahmoud, Tomohiro Nakano, Takanori Iwata, Masayuki Yamato, Teruo Okano and 1 more

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Article in Tissue engineering. Part A, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Orthobiologics: a review.International orthopaedics · 2023
    Review
  7. Article
  8. Review
  9. Article
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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

11 authors at 3 institutions in 1 country.

Ryo Shimizu1 Department of Orthopaedic Surgery, Graduate School of Biomedical & Health Sciences, Hiroshima University , Hiroshima, Japan .
Naosuke Kamei
Nobuo Adachi
Michio Hamanishi
Goki Kamei
Elhussein Elbadry Mahmoud
Tomohiro Nakano
Takanori Iwata
Masayuki Yamato
Teruo Okano
Mitsuo Ochi
Hiroshima University · JPTokyo Women's Medical University · JPHiroshima University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell sheet engineering has developed as a remarkable method for cell transplantation. In the field of cartilage regeneration, several studies previously reported that cartilage defects could be regenerated by transplantation of a chondrocyte sheet using cell sheet engineering. However, it remains unclear how such a thin cell sheet could repair a deep cartilage defect. We, therefore, focused on the mechanism of cartilage repair using cell sheet engineering in this study. Chondrocyte sheets and synovial cell sheets were fabricated using cell sheet engineering, and these allogenic cell sheets were transplanted to cover an osteochondral defect in a rat model. Macroscopic and histological evaluation was performed at 4 and 12 weeks after transplantation. Analysis of the gene expression of each cell sheet and of the regenerated tissue at 1 week after transplantation was performed. In addition, green fluorescent protein (GFP) transgenic rats were used as donors (transplanted chondrocyte sheets) or recipients (osteochondral defect models) to identify the cell origin of regenerated cartilage. Cartilage repair was significantly better in the group implanted with a chondrocyte sheet than in that with a synovial cell sheet. The results of gene expression analysis suggest that the possible factor contributing to cartilage repair might be TGFβ1. Cell tracking experiments using GFP transgenic rats showed that the regenerated cartilage was largely composed of cells derived from the transplanted chondrocyte sheets.

Indexed as

Wound HealingAnimalsBiomedical EngineeringCartilage, ArticularCell TrackingChondrocytesFemurGene Expression RegulationGreen Fluorescent ProteinsImmunohistochemistryRats, Sprague-DawleyRats, TransgenicReal-Time Polymerase Chain ReactionRegenerationStaining and LabelingGreen Fluorescent Proteins

Identifiers

PMID25396711
PMCPMC4356224
OpenAlexW2326639976

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.