The CD200/CD200R mechanism in mesenchymal stem cells' regulation of dendritic cells.

CD200/CD200R Mesenchymal stem cells dendritic cells

Journal

American journal of translational research
ISSN: 1943-8141
Titre abrégé: Am J Transl Res
Pays: United States
ID NLM: 101493030

Informations de publication

Date de publication:
2021
Historique:
received: 27 01 2021
accepted: 12 04 2021
entrez: 20 9 2021
pubmed: 21 9 2021
medline: 21 9 2021
Statut: epublish

Résumé

To investigate the CD200/CD200R pathway mechanism in mesenchymal stem cells' (MSC) regulation of dendritic cells (DC) (MSc). We collected marrow samples from 40 patients admitted to our hospital from January 2018 to December 2019. The bone marrow MSCs were cultivated, and the peripheral blood mononuclear cells (PBMC) and peripheral blood DC were isolated to establish an in vitro immune response model. The expressions of the CD200 molecule on the surface of MSC were measured. Anti-CD200 blocking antibodies were added to the culture system to observe the effect of the PBMC differentiation and the immature DC (imDC) to mature DC (mDC). Then the impact of the different positive rates of CD200 in the same MSC on imDC maturity was measured. After adding mitogen pHA, the IL-4, IL-10, and TNF-α secretions were increased (all P<0.05), and the OD value of the PBMC+pHA group was higher than it was in the PBMC group. After stimulated by pHA, the CD200 of the MSC group was higher than it was in the MSC+PBMC group (P<0.05). The MSC+PBMC group co-culture inhibited the development of imDC to mDC. Adding anti-CD200 antibodies to the MSC+PBMC co-culture system, MSC could still inhibit the differentiation of PBMC to imDC, and MSC had a significant inhibition effect on imDC to mDC maturation (P=0.006). The addition of MSC reduces the maturation markers on the surface of mDC (P<0.05). The addition of MSC inhibited the ability of mDC to stimulate PBMC (P The mechanism by which MSC inhibits DC may be achieved through the CD200/CD200R pathway, and the CD200/CD200R pathway mainly acts on the process from imDC to mDC.

Identifiants

pubmed: 34540085
pmc: PMC8430165

Types de publication

Journal Article

Langues

eng

Pagination

9607-9613

Informations de copyright

AJTR Copyright © 2021.

Déclaration de conflit d'intérêts

None.

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Auteurs

Yulei Zhao (Y)

The Second Department of Hematology, Cangzhou Central Hospital 16 West Xinhua Road, Yunhe, Cangzhou, China.

Guohong Su (G)

The Second Department of Hematology, Cangzhou Central Hospital 16 West Xinhua Road, Yunhe, Cangzhou, China.

Qing Wang (Q)

The Second Department of Hematology, Cangzhou Central Hospital 16 West Xinhua Road, Yunhe, Cangzhou, China.

Ruihuan Wang (R)

The Second Department of Hematology, Cangzhou Central Hospital 16 West Xinhua Road, Yunhe, Cangzhou, China.

Minjuan Zhang (M)

The Second Department of Hematology, Cangzhou Central Hospital 16 West Xinhua Road, Yunhe, Cangzhou, China.

Classifications MeSH