Evidence map›Paper›PMID 28230853›Full record

ArticleCell death & disease2017

Mesenchymal stromal cells inhibit CD25 expression via the mTOR pathway to potentiate T-cell suppression.

Hyun Seung Yoo, Kyuheon Lee, Kwangmin Na, Yong Xu Zhang, Hyun-Ja Lim, TacGhee Yi, Sun U Song, Myung-Shin Jeon

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

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  14. The energy sensor AMPK orchestrates metabolic and translational adaptation in expanding T helper cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
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  19. Translational Control in Cancer.Cold Spring Harbor perspectives in biology · 2019
    Review
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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

8 authors at 1 institution in 1 country.

Hyun Seung YooDepartment of Molecular Biomedicine, Translational Research Center, Inha University Hospital, IRIMS, Inha University School of Medicine, Incheon 22332, Republic of Korea.
Kyuheon LeeDepartment of Molecular Biomedicine, Translational Research Center, Inha University Hospital, IRIMS, Inha University School of Medicine, Incheon 22332, Republic of Korea.
Kwangmin NaDepartment of Molecular Biomedicine, Translational Research Center, Inha University Hospital, IRIMS, Inha University School of Medicine, Incheon 22332, Republic of Korea.
Yong Xu ZhangDepartment of Molecular Biomedicine, Translational Research Center, Inha University Hospital, IRIMS, Inha University School of Medicine, Incheon 22332, Republic of Korea.
Hyun-Ja LimSCM Lifescience Co., Ltd., Incheon 22332, Republic of Korea.
TacGhee YiDepartment of Molecular Biomedicine, Translational Research Center, Inha University Hospital, IRIMS, Inha University School of Medicine, Incheon 22332, Republic of Korea.
Sun U SongDepartment of Molecular Biomedicine, Translational Research Center, Inha University Hospital, IRIMS, Inha University School of Medicine, Incheon 22332, Republic of Korea.
Myung-Shin JeonDepartment of Molecular Biomedicine, Translational Research Center, Inha University Hospital, IRIMS, Inha University School of Medicine, Incheon 22332, Republic of Korea.
Inha University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stromal cells (MSCs) are known to suppress T-cell activation and proliferation. Several studies have reported that MSCs suppress CD25 expression in T cells. However, the molecular mechanism underlying MSC-mediated suppression of CD25 expression has not been fully examined. Here, we investigated the mTOR pathway, which is involved in CD25 expression in T cells. We showed that MSCs inhibited CD25 expression, which was restored in the presence of an inducible nitric oxide synthase (iNOS) inhibitor. Since CD25 mRNA expression was not inhibited, we focused on determining whether MSCs modulated components of the mTOR pathway in T cells. MSCs increased the phosphorylation of liver kinase B1 (LKB1) and AMP-activated protein kinase (AMPK) and decreased the phosphorylation of ribosomal protein S6 kinase 1 (S6K1) and eukaryotic translation initiation factor 4E-binding protein 1 (4E-BP1). In addition, the expression of 4E-BP1 increased dramatically in the presence of MSCs. An m

Indexed as

AMP-Activated Protein KinasesAnimalsCarrier ProteinsCell LineInterleukin-2 Receptor alpha SubunitMesenchymal Stem CellsMiceMice, Inbred BALB CMice, Inbred C3HMice, Inbred C57BLNitric OxideNitric Oxide Synthase Type IIProtein Serine-Threonine KinasesRibosomal Protein S6 Kinases, 90-kDaRNA, MessengerSignal TransductionAMP-Activated Protein KinasesCarrier ProteinsIl2ra protein, mouseInterleukin-2 Receptor alpha SubunitmTOR protein, mouseNitric OxideNitric Oxide Synthase Type IIProtein Serine-Threonine KinasesRibosomal Protein S6 Kinases, 90-kDaRNA, MessengerTOR Serine-Threonine Kinases

Identifiers

PMID28230853
PMCPMC5386489
OpenAlexW2591362217

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.