Evidence map›Paper›PMID 32448932›Full record

ArticlePediatric surgery international2020

Therapeutic potential of mature adipocyte-derived dedifferentiated fat cells for inflammatory bowel disease.

Shigeki Ishioka, Takashi Hosokawa, Taro Ikeda, Noriyoshi Konuma, Hide Kaneda, Kensuke Ohashi, Takeshi Furuya, Takayuki Masuko, Hiroaki Taniguchi, Koichiro Kano and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Pediatric surgery international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 9 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 4 institutions in 2 countries.

Shigeki IshiokaDepartment of Pediatric Surgery, Nihon University School of Medicine, Tokyo, 173-8610, Japan.
Takashi HosokawaDepartment of Pediatric Surgery, Nihon University School of Medicine, Tokyo, 173-8610, Japan.
Taro IkedaDepartment of Surgery, Saitama Medical Center, Jichi Medical University, Saitama, 330-8503, Japan.
Noriyoshi KonumaDepartment of Pediatric Surgery, Nihon University School of Medicine, Tokyo, 173-8610, Japan.
Hide KanedaDepartment of Pediatric Surgery, Nihon University School of Medicine, Tokyo, 173-8610, Japan.
Kensuke OhashiDepartment of Pediatric Surgery, Nihon University School of Medicine, Tokyo, 173-8610, Japan.
Takeshi FuruyaDepartment of Pediatric Surgery, Nihon University School of Medicine, Tokyo, 173-8610, Japan.
Takayuki MasukoPediatric Surgery and Urology, Ibaraki Children's Hospital, Mito, 311-4145, Japan.
Hiroaki TaniguchiInstitute of Genetics and Animal Breeding of the Polish Academy of Sciences, 05-552, Magdalenka, Poland.
Koichiro KanoLaboratory of Cell and Tissue Biology, College of Bioresource Science, Nihon University, Fujisawa, 252-0880, Japan.
Tsugumichi KoshinagaDepartment of Pediatric Surgery, Nihon University School of Medicine, Tokyo, 173-8610, Japan.
Taro MatsumotoDivision of Cell Regeneration and Transplantation, Department of Functional Morphology, Nihon University School of Medicine, 30-1 Ohyaguchikami-cho, Itabashi-ku, Tokyo, 173-8610, Japan. matsumoto.taro@nihon-u.ac.jp.ORCID http://orcid.org/0000-0002-2965-2673
Nihon University · JPIbaraki Children's Hospital · JPJichi Medical University · JPPolish Academy of Sciences · PL

Funding

JSPS KAKENHI 16K11356JSPS KAKENHI 17H04152JSPS KAKENHI 19K09058JSPS KAKENHI 22791714Ministry of Education, Culture, Sports, Science and Technology S1411018Nihon University President Grant Initiative 2018-2020
6 · The paper itself

Abstract

purposeOur previous studies demonstrated that mature adipocyte-derived dedifferentiated fat (DFAT) cells possess similar multipotency as mesenchymal stem cells. Here, we examined the immunoregulatory potential of DFAT cells in vitro and the therapeutic effect of DFAT cell transplantation in a mouse inflammatory bowel disease (IBD) model.

methodsThe effect of DFAT cell co-culture on T cell proliferation and expression of immunosuppression-related genes in DFAT cells were evaluated. To create IBD, CD4

resultsThe T cell proliferation was inhibited by co-cultured DFAT cells in a cell density-dependent manner. Gene expression of TRAIL, IDO1, and NOS2 in DFAT cells was upregulated by TNFα stimulation. DFAT group improved IBD-associated weight loss, IBD clinical and histological scores compared to Control group.

conclusionDFAT cells possess immunoregulatory potential and the cell transplantation promoted recovery from colon damage and improved clinical symptoms in the IBD model. DFAT cells could play an important role in the treatment of IBD.

Indexed as

AdipocytesAnimalsCell Culture TechniquesCell DedifferentiationCell ProliferationCell TransplantationDisease Models, AnimalFemaleInflammatory Bowel DiseasesMiceMice, Inbred BALB CAdipocytesInflammatory bowel diseasesMesenchymal stromal cellsRegenerative medicine

Identifiers

PMID32448932
PMCPMC7292821
OpenAlexW3028252369

What OpenQuestion holds

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LicenceCC BY
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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.