Evidence map›Paper›PMID 25561682›Full record

ArticleStem cells translational medicine2015

Therapeutic Potential of Adipose-Derived SSEA-3-Positive Muse Cells for Treating Diabetic Skin Ulcers.

Kahori Kinoshita, Shinichiro Kuno, Hisako Ishimine, Noriyuki Aoi, Kazuhide Mineda, Harunosuke Kato, Kentaro Doi, Koji Kanayama, Jingwei Feng, Takanobu Mashiko and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
7.3field-weighted citation impact, top 2% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Kahori KinoshitaDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Shinichiro KunoDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Hisako IshimineDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Noriyuki AoiDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Kazuhide MinedaDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Harunosuke KatoDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Kentaro DoiDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Koji KanayamaDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Jingwei FengDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Takanobu MashikoDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Akira KurisakiDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan.
Kotaro YoshimuraDepartment of Plastic Surgery, University of Tokyo Graduate School of Medicine, Tokyo, Japan; Research Center for Stem Cell Engineering, National Institute for Advanced Industrial Science and Technology, Ibaraki, Japan kotaro-yoshimura@umin.ac.jp.
The University of Tokyo · JPNational Institute of Advanced Industrial Science and Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stage-specific embryonic antigen-3 (SSEA-3)-positive multipotent mesenchymal cells (multilineage differentiating stress-enduring [Muse] cells) were isolated from cultured human adipose tissue-derived stem/stromal cells (hASCs) and characterized, and their therapeutic potential for treating diabetic skin ulcers was evaluated. Cultured hASCs were separated using magnetic-activated cell sorting into positive and negative fractions, a SSEA-3+ cell-enriched fraction (Muse-rich) and the remaining fraction (Muse-poor). Muse-rich hASCs showed upregulated and downregulated pluripotency and cell proliferation genes, respectively, compared with Muse-poor hASCs. These cells also released higher amounts of certain growth factors, particularly under hypoxic conditions, compared with Muse-poor cells. Skin ulcers were generated in severe combined immunodeficiency (SCID) mice with type 1 diabetes, which showed delayed wound healing compared with nondiabetic SCID mice. Treatment with Muse-rich cells significantly accelerated wound healing compared with treatment with Muse-poor cells. Transplanted cells were integrated into the regenerated dermis as vascular endothelial cells and other cells. However, they were not detected in the surrounding intact regions. Thus, the selected population of ASCs has greater therapeutic effects to accelerate impaired wound healing associated with type 1 diabetes. These cells can be achieved in large amounts with minimal morbidity and could be a practical tool for a variety of stem cell-depleted or ischemic conditions of various organs and tissues.

Indexed as

Mesenchymal Stem Cell TransplantationAdipose TissueAdolescentAdultAnimalsAntigens, Tumor-Associated, CarbohydrateDiabetes ComplicationsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1FemaleHeterograftsHumansMesenchymal Stem CellsMice, SCIDMultipotent Stem CellsSkin UlcerAntigens, Tumor-Associated, Carbohydratestage-specific embryonic antigen-3Stage-Specific Embryonic AntigensAdiposeAdult stem cellsCell cultureEndothelial cellHyaluronanMesenchymal stem cellsStem cell transplantationTissue regeneration

Identifiers

PMID25561682
PMCPMC4303359
OpenAlexW2031893661

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.