Evidence map›Paper›PMID 33122466›Full record

ArticleInternational journal of stem cells2021

TL1A/TNFR2 Axis Enhances Immunoregulatory Effects of Bone Marrow Derived Mesenchymal Stem Cell by Indian Hedgehog Signaling Pathway.

Mahmoud Al-Azab, Williams Walana, Jing Wei, Weiping Li, Yawei Tang, Xiaoqing Wei, Marwan Almoiliqy, Abdullah Shopit, Elrayah Eltahir Abbas, Salah Adlat and 3 more

Abstract read
In one paragraph

Article in International journal of stem cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. 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

13 authors.

Mahmoud Al-AzabDepartment of Immunology, College of Basic Medical Science, Dalian Medical University, Liaoning, China.
Williams WalanaDepartment of Immunology, College of Basic Medical Science, Dalian Medical University, Liaoning, China.
Jing WeiDepartment of Immunology, College of Basic Medical Science, Dalian Medical University, Liaoning, China.
Weiping LiDepartment of Immunology, College of Basic Medical Science, Dalian Medical University, Liaoning, China.
Yawei TangDepartment of Immunology, College of Basic Medical Science, Dalian Medical University, Liaoning, China.
Xiaoqing WeiMolecular Medicine Laboratory, College of Basic Medical Science, Dalian Medical University, Liaoning, China.
Marwan AlmoiliqyDepartment of Pharmacology, College of Pharmacy, Dalian Medical University, Liaoning, China.
Abdullah ShopitDepartment of Pharmacology, College of Pharmacy, Dalian Medical University, Liaoning, China.
Elrayah Eltahir AbbasMicrobiology Laboratory, College of Basic Medical Science, Dalian Medical University, Liaoning, China.
Salah AdlatKey Laboratory of Molecular Epigenetics of MOE, School of Life Science, Northeast Normal University, Changchun, China.
Mohammed AwshDepartment of Pharmacology, College of Pharmacy, Dalian Medical University, Liaoning, China.
Xia LiDepartment of Immunology, College of Basic Medical Science, Dalian Medical University, Liaoning, China.
Bing WangDepartment of Immunology, College of Basic Medical Science, Dalian Medical University, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe immunomodulatory potential of mesenchymal stem cells (MSCs) can be regulated by a variety of molecules, especially cytokines. The inflammatory cytokine, TNF-like ligand 1A (TL1A), has been reported as an inflammation stimulator in-multiple autoimmune diseases. Here, we studied the effects of TL1A/TNF-receptor 2 (TNFR2) pathway on the therapeutic potency of bone marrow-derived MSCs (BMSCs). METHODS AND

resultsBMSCs, fibroblast-like synoviocytes (FLSs), and H9 and jurkat human T lymphocytes were used in this study. BMSCs paracrine activities, differentiation, proliferation, and migration were investigated after stimulation with TL1A, and intervened with anti-TNFR2. Additionally, the effects of TL1A on BMSCs therapeutic potency were evaluated by treating RA-FLSs, and H9 and jurkat T cells with TL1A-stimulated BMSCs conditioned medium (CM). Indian hedgehog (IHH) involvement was determined by gene silencing and treatment by recombinant IHH (rIHH). TL1A induced BMSCs stemness-related genes, COX-2, IL-6, IDO, TGF-

conclusionsThis study reports the effects of TL1A/TNFR2 pathway on the biological behaviors and therapeutic potency of BMSCs through IHH. These findings could introduce novel procedures to increase the stemness of MSCs in cellular therapy.

Indexed as

Bone marrow-derived mesenchymal stem cellsIndian hedgehogTNF-receptor 2Tumor necrosis factor-like ligand 1A

Identifiers

PMID33122466
PMCPMC7904531

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.