Evidence map›Paper›PMID 36260750›Full record

ArticleLife science alliance2022

Cross talk between glucose metabolism and immunosuppression in IFN-γ-primed mesenchymal stem cells.

Mengwei Yao, Zhuo Chen, Xiao He, Jiaoyue Long, Xuewei Xia, Zhan Li, Yu Yang, Luoquan Ao, Wei Xing, Qizhou Lian and 2 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  5. Hypoxia-Induced Suppression of FAM99A and FAM99B Contributes to the Development and Glucose Metabolic Reprogramming of Hepatocellular Carcinoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
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  7. WTAP/YTHDF1-mediated mJournal of advanced research · 2025
    Article
  8. Review
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  12. Article
  13. Article
  14. Review
  15. Macrophages-bone marrow mesenchymal stem cells crosstalk in bone healing.Frontiers in cell and developmental biology · 2023
    Review
  16. Review
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 2 countries.

Mengwei YaoDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China.ORCID 0000-0002-7484-8552
Zhuo ChenDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China.
Xiao HePLA Rocket Force Characteristic Medical Center, Beijing, China.ORCID 0000-0002-0308-0910
Jiaoyue LongDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China.
Xuewei XiaDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China.
Zhan LiDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China.
Yu YangDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China.
Luoquan AoDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China.
Wei XingDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China.
Qizhou LianHKUMed Laboratory of Cellular Therapeutics, and State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Pok Fu Lam, Hong Kong.
Huaping LiangDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China xiangxu@tmmu.edu.cn 13638356728@163.com.ORCID 0000-0003-4157-445X
Xiang XuDepartment of Stem Cell and Regenerative Medicine, Daping Hospital, Army Medical University, Chongqing, China xiangxu@tmmu.edu.cn 13638356728@163.com.ORCID 0000-0002-1026-2210
Army Medical University · CNGuangzhou Women and Children Medical Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The immunosuppressive function "licensed" by IFN-γ is a vital attribute of mesenchymal stem cells (MSCs) widely used in the treatment of inflammatory diseases. However, the mechanism and impact of metabolic reprogramming on MSC immunomodulatory plasticity remain unclear. Here, we explored the mechanism by which glucose metabolism affects the immunomodulatory reprogramming of MSCs "licensed" by IFN-γ. Our data showed that glucose metabolism regulates the immunosuppressive function of human umbilical cord MSCs (hUC-MSCs) challenged by IFN-γ through the Janus kinase-signal transducer and activator of transcription (JAK-STAT) pathway. Furthermore, ATP facilitated the cross talk between glucose metabolism and the JAK-STAT system, which stimulates the phosphorylation of JAK2 and STATs, as well as the expression of indoleamine 2, 3-dioxygenase and programmed cell death-1 ligand. Moreover, ATP synergistically enhanced the therapeutic efficacy of IFN-γ-primed hUC-MSCs against acute pneumonia in mice. These results indicate a novel cross talk between the immunosuppressive function, glucose metabolism, and mitochondrial oxidation and provide a novel targeting strategy to enhance the therapeutic efficacies of hUC-MSCs.

Indexed as

DioxygenasesMesenchymal Stem CellsAdenosine TriphosphateAnimalsGlucoseHumansImmunosuppression TherapyInterferon-gammaJanus KinasesLigandsMiceAdenosine TriphosphateDioxygenasesGlucoseInterferon-gammaJanus KinasesLigands

Identifiers

PMID36260750
PMCPMC9463493
OpenAlexW4295028047

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.