Evidence map›Paper›PMID 27221006›Full record

ArticleMolecular medicine reports2016

TNF-α enhances vascular cell adhesion molecule-1 expression in human bone marrow mesenchymal stem cells via the NF-κB, ERK and JNK signaling pathways.

Zi-Yuan Lu, Wan-Cheng Chen, Yong-Hua Li, Li Li, Hang Zhang, Yan Pang, Zhi-Fang Xiao, Hao-Wen Xiao, Yang Xiao

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.2field-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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  4. Review
  5. TNF-α Limits Serological Memory by Disrupting the Bone Marrow Niche.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
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  14. Article
  15. CRISPR-Based Activation of Endogenous Expression ofFrontiers in cell and developmental biology · 2021
    Article
  16. Article
  17. Article
  18. Review
  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

9 authors at 2 institutions in 1 country.

Zi-Yuan LuFirst School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
Wan-Cheng ChenFirst School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
Yong-Hua LiDepartment of Hematology, General Hospital of Guangzhou Military Command of Chinese PLA, Guangzhou, Guangdong 510010, P.R. China.
Li LiDepartment of Hematology, General Hospital of Guangzhou Military Command of Chinese PLA, Guangzhou, Guangdong 510010, P.R. China.
Hang ZhangDepartment of Hematology, General Hospital of Guangzhou Military Command of Chinese PLA, Guangzhou, Guangdong 510010, P.R. China.
Yan PangDepartment of Hematology, General Hospital of Guangzhou Military Command of Chinese PLA, Guangzhou, Guangdong 510010, P.R. China.
Zhi-Fang XiaoDepartment of Hematology, General Hospital of Guangzhou Military Command of Chinese PLA, Guangzhou, Guangdong 510010, P.R. China.
Hao-Wen XiaoDepartment of Hematology, General Hospital of Guangzhou Military Command of Chinese PLA, Guangzhou, Guangdong 510010, P.R. China.
Yang XiaoFirst School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
General Hospital of Guangzhou Military Command · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The migration of circulating mesenchymal stem cells (MSCs) to injured tissue is an important step in tissue regeneration and requires adhesion to the microvascular endothelium. The current study investigated the underlying mechanism of MSC adhesion to endothelial cells during inflammation. In in vitro MSC culture, tumor necrosis factor‑α (TNF‑α) increased the level of vascular cell adhesion molecule‑1 (VCAM‑1) expression in a dose‑dependent manner. The nuclear factor-κB (NF-κB), extracellular signal‑regulated kinase (ERK) and c‑Jun N‑terminal kinase (JNK) signaling pathway inhibitors, pyrrolidine dithiocarbamate (PDTC), U0126 and SP600125, respectively, suppressed VCAM‑1 expression induced by TNF‑α at the mRNA and protein levels (P<0.05). TNF‑α augmented the activation of NF‑κB, ERK and JNK, and promoted MSC adhesion to human umbilical vein endothelial cells; however, the inhibitors of NF‑κB, ERK and JNK did not affect this process in these cells. The results of the current study indicate that adhesion of circulating MSCs to the endothelium is regulated by TNF-α-induced VCAM-1 expression, which is potentially mediated by the NF‑κB, ERK and JNK signaling pathways.

Indexed as

Signal TransductionAnthracenesBiomarkersButadienesCell AdhesionDose-Response Relationship, DrugExtracellular Signal-Regulated MAP KinasesGene Expression RegulationHumansHuman Umbilical Vein Endothelial CellsImmunophenotypingJNK Mitogen-Activated Protein KinasesMesenchymal Stem CellsNF-kappa BNitrilesPhosphorylationAnthracenesBiomarkersButadienesExtracellular Signal-Regulated MAP KinasesJNK Mitogen-Activated Protein KinasesNF-kappa BNitrilespyrazolanthroneTumor Necrosis Factor-alphaU 0126Vascular Cell Adhesion Molecule-1

Identifiers

PMID27221006
PMCPMC4918617
OpenAlexW2397932615

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.