Evidence map›Paper›PMID 27444207›Full record

ArticleScientific reports2016

TSG-6 secreted by human umbilical cord-MSCs attenuates severe burn-induced excessive inflammation via inhibiting activations of P38 and JNK signaling.

Lingying Liu, Huifeng Song, Hongjie Duan, Jiake Chai, Jing Yang, Xiao Li, Yonghui Yu, Xulong Zhang, Xiaohong Hu, Mengjing Xiao and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed, 60 citations in OpenAlex.

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  7. Influence of Umbilical Cord Blood Biochemical Parameters and Disease Condition on the Expression of the TSG-6 Gene in Umbilical Mesenchymal Stem Cells.Medical science monitor : international medical journal of experimental and clinical research · 2023
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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

16 authors at 1 institution in 1 country.

Lingying LiuDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Huifeng SongDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Hongjie DuanDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Jiake ChaiDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Jing YangDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Xiao LiDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Yonghui YuDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Xulong ZhangDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Xiaohong HuDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Mengjing XiaoDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Rui FengDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Huinan YinDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Quan HuDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Longlong YangDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Jundong DuDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
Tianran LiDepartment of Burn &Plastic Surgery, the First Affiliated Hospital to PLA General Hospital.
First Affiliated Hospital of Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hMSCs have become a promising approach for inflammation treatment in acute phase. Our previous study has demonstrated that human umbilical cord-MSCs could alleviate the inflammatory reaction of severely burned wound. In this study, we further investigated the potential role and mechanism of the MSCs on severe burn-induced excessive inflammation. Wistar rats were randomly divided into following groups: Sham, Burn, Burn+MSCs, Burn+MAPKs inhibitors, and Burn, Burn+MSCs, Burn+Vehicle, Burn+siTSG-6, Burn+rhTSG-6 in the both experiments. It was found that MSCs could only down-regulate P38 and JNK signaling, but had no effect on ERK in peritoneal macrophages of severe burn rats. Furthermore, suppression of P38 and JNK activations significantly reduced the excessive inflammation induced by severe burn. TSG-6 was secreted by MSCs using different inflammatory mediators. TSG-6 from MSCs and recombinant human (rh)TSG-6 all significantly reduced activations of P38 and JNK signaling induced by severe burn and then attenuated excessive inflammations. On the contrary, knockdown TSG-6 in the cells significantly increased phosphorylation of P38 and JNK signaling and reduced therapeutic effect of the MSCs on excessive inflammation. Taken together, this study suggested TSG-6 from MSCs attenuated severe burn-induced excessive inflammation via inhibiting activation of P38 and JNK signaling.

Indexed as

AnimalsBiological TransportBurnsCell Adhesion MoleculesCells, CulturedHumansInflammationMaleMAP Kinase Signaling SystemMesenchymal Stem Cellsp38 Mitogen-Activated Protein KinasesPhosphorylationProtein Kinase InhibitorsRatsRats, WistarSignal TransductionCell Adhesion Moleculesp38 Mitogen-Activated Protein KinasesProtein Kinase InhibitorsTNFAIP6 protein, human

Identifiers

PMID27444207
PMCPMC4957124
OpenAlexW2483172171

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Registered trials

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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.