Evidence map›Paper›PMID 30359308›Full record

ArticleStem cell research & therapy2018

Induction of CD4

Maryam Khosravi, Ali Bidmeshkipour, José L Cohen, Ali Moravej, Suzzan Hojjat-Assari, Sina Naserian, Mohammad Hossein Karimi

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

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  6. Development of stem cell therapy for atherosclerosis.Molecular and cellular biochemistry · 2024
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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

7 authors at 6 institutions in 2 countries.

Maryam KhosraviTransplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Ali BidmeshkipourDepartment of Biology, Faculty of Science, Razi University, Kermanshah, Iran.
José L CohenUniversité Paris-Est, UMR_S955, UPEC, F-94000, Créteil, France.
Ali MoravejNoncommunicable Diseases Research Centre, Fasa University of Medical Sciences, Fasa, Iran.
Suzzan Hojjat-AssariInstitut Français de Recherche et d'Enseignement Supérieur à l'International (IFRES-INT), Paris, France.
Sina NaserianUniversité Paris-Est, UMR_S955, UPEC, F-94000, Créteil, France.
Mohammad Hossein KarimiTransplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. karimimh@sums.ac.ir.
Razi University · IRFasa University of Medical Sciences · IRHôpital Paul-Brousse · FRInserm · FRInstitut Français des Relations Internationales · FRShiraz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) are known for their ability to induce the conversion of conventional T cells (Tconvs) into induced regulatory T cells (iTregs) in specific inflammatory contexts. Stable Foxp3 expression plays a major role in the phenotypic and functional stability of iTregs. However, how MSCs induce stable Foxp3 expression remains unknown.

methodsWe first investigated the role of cell-cell contact and cytokine secretion by bone marrow-derived MSCs (BM-MSCs) on the induction, stability, and suppressive functions of Tregs under various experimental conditions that lead to Foxp3 generation by flow cytometry and ELISA respectively. Second, we studied the effect of MSCs on TRAF6, GRAIL, USP7, STUB1, and UBC13 mRNA expression in CD4

resultsWe found that in-vitro MSC-induced Tregs express high mRNA levels of ubiquitination genes such as TRAF6, GRAIL, and USP7 and low levels of STUB1. Moreover, they have enhanced TSDR demethylation. Infusion of MSCs in a murine model of allogeneic skin transplantation prolonged allograft survival. When CD4

conclusionsOur data suggest a possible ubiquitination mechanism by which MSCs convert Tconvs to suppressive and stable iTregs.

Indexed as

Skin TransplantationAnimalsAntigens, LyBiomarkersCD4 AntigensCoculture TechniquesDemethylationFemaleFemurForkhead Transcription FactorsGene Expression RegulationHyaluronan ReceptorsInterleukin-2 Receptor alpha SubunitMembrane ProteinsMesenchymal Stem CellsMiceAntigens, LyBiomarkersCd44 protein, mouseCD4 AntigensForkhead Transcription FactorsFoxp3 protein, mouseHyaluronan ReceptorsInterleukin-2 Receptor alpha SubunitLy6a protein, mouseMembrane ProteinsRNF128 protein, mouseStub1 protein, mouseTNF Receptor-Associated Factor 6Ubiquitin-Protein LigasesUbiquitin-Specific Peptidase 7Usp7 protein, mouseMesenchymal stem cellsRegulatory T cellsUbiquitination molecules

Identifiers

PMID30359308
PMCPMC6203284
OpenAlexW2898362420

What OpenQuestion holds

Textmetadata
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.