Evidence map›Paper›PMID 28553282›Full record

ArticleFrontiers in immunology2017

Co-Inflammatory Roles of TGFβ1 in the Presence of TNFα Drive a Pro-inflammatory Fate in Mesenchymal Stem Cells.

Shalom Lerrer, Yulia Liubomirski, Alexander Bott, Khalid Abnaof, Nino Oren, Afsheen Yousaf, Cindy Körner, Tsipi Meshel, Stefan Wiemann, Adit Ben-Baruch

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. The application potential of iMSCs and iMSC-EVs in diseases.Frontiers in bioengineering and biotechnology · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Partners in crime: TNFα-based networks promoting cancer progression.Cancer immunology, immunotherapy : CII · 2020
    Review
  17. Review
  18. Article
  19. Article
  20. Article
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

10 authors at 3 institutions in 2 countries.

Shalom LerrerFaculty of Life Sciences, Department of Cell Research and Immunology, Tel Aviv University, Tel Aviv, Israel.
Yulia LiubomirskiFaculty of Life Sciences, Department of Cell Research and Immunology, Tel Aviv University, Tel Aviv, Israel.
Alexander BottDivision of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Khalid AbnaofDivision of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Nino OrenFaculty of Life Sciences, Department of Cell Research and Immunology, Tel Aviv University, Tel Aviv, Israel.
Afsheen YousafDivision of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Cindy KörnerDivision of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Tsipi MeshelFaculty of Life Sciences, Department of Cell Research and Immunology, Tel Aviv University, Tel Aviv, Israel.
Stefan WiemannDivision of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Adit Ben-BaruchFaculty of Life Sciences, Department of Cell Research and Immunology, Tel Aviv University, Tel Aviv, Israel.
Tel Aviv University · ILGerman Cancer Research Center · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High plasticity is a hallmark of mesenchymal stem cells (MSCs), and as such, their differentiation and activities may be shaped by factors of their microenvironment. Bones, tumors, and cardiomyopathy are examples of niches and conditions that contain MSCs and are enriched with tumor necrosis factor α (TNFα) and transforming growth factor β1 (TGFβ1). These two cytokines are generally considered as having opposing roles in regulating immunity and inflammation (pro- and anti-inflammatory, respectively). Here, we performed global gene expression analysis of human bone marrow-derived MSCs and identified overlap in half of the transcriptional programs that were modified by TNFα and TGFβ1. The two cytokines elevated the mRNA expression of soluble factors, including mRNAs of pro-inflammatory mediators. Accordingly, the typical pro-inflammatory factor TNFα prominently induced the protein expression levels of the pro-inflammatory mediators CCL2, CXCL8 (IL-8), and cyclooxygenase-2 (Cox-2) in MSCs, through the NF-κB/p65 pathway. In parallel, TGFβ1 did not elevate CXCL8 protein levels and induced the protein expression of CCL2 at much lower levels than TNFα; yet, TGFβ1 readily induced Cox-2 and acted predominantly

Indexed as

bone marrow-derived mesenchymal stem cellsNF-κBpro-inflammatory mediatorsSmad3TGFβ1TNFα

Identifiers

PMID28553282
PMCPMC5425596
OpenAlexW2613238640

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.