Mechanisms behind the Immunoregulatory Dialogue between Mesenchymal Stem Cells and Th17 Cells.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
10 07 2020
Historique:
received: 23 05 2020
revised: 03 07 2020
accepted: 05 07 2020
entrez: 16 7 2020
pubmed: 16 7 2020
medline: 13 4 2021
Statut: epublish

Résumé

Mesenchymal stem cells (MSCs) exhibit potent immunoregulatory abilities by interacting with cells of the adaptive and innate immune system. In vitro, MSCs inhibit the differentiation of T cells into T helper 17 (Th17) cells and repress their proliferation. In vivo, the administration of MSCs to treat various experimental inflammatory and autoimmune diseases, such as rheumatoid arthritis, type 1 diabetes, multiple sclerosis, systemic lupus erythematosus, and bowel disease showed promising therapeutic results. These therapeutic properties mediated by MSCs are associated with an attenuated immune response characterized by a reduced frequency of Th17 cells and the generation of regulatory T cells. In this manuscript, we review how MSC and Th17 cells interact, communicate, and exchange information through different ways such as cell-to-cell contact, secretion of soluble factors, and organelle transfer. Moreover, we discuss the consequences of this dynamic dialogue between MSC and Th17 well described by their phenotypic and functional plasticity.

Identifiants

pubmed: 32664207
pii: cells9071660
doi: 10.3390/cells9071660
pmc: PMC7408034
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Claudia Terraza-Aguirre (C)

IRMB, University of Montpellier, INSERM, F-34090 Montpellier, France.

Mauricio Campos-Mora (M)

IGH, University of Montpellier, CNRS, F-34396 Montpellier, France.

Roberto Elizondo-Vega (R)

Facultad de Ciencias Biológicas, Departamento de Biología Celular, Laboratorio de Biología Celular, Universidad de Concepción, Concepción 4030000, Chile.

Rafael A Contreras-López (RA)

IRMB, University of Montpellier, INSERM, F-34090 Montpellier, France.

Patricia Luz-Crawford (P)

Centro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago 7620001, Chile.

Christian Jorgensen (C)

IRMB, University of Montpellier, INSERM, F-34090 Montpellier, France.
CHU Montpellier, F-34295 Montpellier, France.

Farida Djouad (F)

IRMB, University of Montpellier, INSERM, F-34090 Montpellier, France.

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