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Immunosuppressive Property of MSCs Mediated by Cell Surface Receptors
In the past decade, mesenchymal stem cells (MSCs) tend to exhibit inherent tropism for refractory inflammatory diseases and engineered MSCs have appeared on the market as therapeutic agents. Recently, engineered MSCs target to cell surface molecules on immune cells has been a new strategy to improve...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399134/ https://www.ncbi.nlm.nih.gov/pubmed/32849489 http://dx.doi.org/10.3389/fimmu.2020.01076 |
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author | Liu, Siyu Liu, Fei Zhou, You Jin, Baeku Sun, Qiang Guo, Shu |
author_facet | Liu, Siyu Liu, Fei Zhou, You Jin, Baeku Sun, Qiang Guo, Shu |
author_sort | Liu, Siyu |
collection | PubMed |
description | In the past decade, mesenchymal stem cells (MSCs) tend to exhibit inherent tropism for refractory inflammatory diseases and engineered MSCs have appeared on the market as therapeutic agents. Recently, engineered MSCs target to cell surface molecules on immune cells has been a new strategy to improve MSC applications. In this review, we discuss the roles of multiple receptors (ICAM-1, Gal-9, PD-L1, TIGIT, CD200, and CXCR4) in the process of MSCs' immunosuppressive properties. Furthermore, we discuss the principles and strategies for developing receptor-regulated MSCs and their mechanisms of action and the challenges of using MSCs as immunosuppressive therapies. |
format | Online Article Text |
id | pubmed-7399134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73991342020-08-25 Immunosuppressive Property of MSCs Mediated by Cell Surface Receptors Liu, Siyu Liu, Fei Zhou, You Jin, Baeku Sun, Qiang Guo, Shu Front Immunol Immunology In the past decade, mesenchymal stem cells (MSCs) tend to exhibit inherent tropism for refractory inflammatory diseases and engineered MSCs have appeared on the market as therapeutic agents. Recently, engineered MSCs target to cell surface molecules on immune cells has been a new strategy to improve MSC applications. In this review, we discuss the roles of multiple receptors (ICAM-1, Gal-9, PD-L1, TIGIT, CD200, and CXCR4) in the process of MSCs' immunosuppressive properties. Furthermore, we discuss the principles and strategies for developing receptor-regulated MSCs and their mechanisms of action and the challenges of using MSCs as immunosuppressive therapies. Frontiers Media S.A. 2020-07-28 /pmc/articles/PMC7399134/ /pubmed/32849489 http://dx.doi.org/10.3389/fimmu.2020.01076 Text en Copyright © 2020 Liu, Liu, Zhou, Jin, Sun and Guo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Liu, Siyu Liu, Fei Zhou, You Jin, Baeku Sun, Qiang Guo, Shu Immunosuppressive Property of MSCs Mediated by Cell Surface Receptors |
title | Immunosuppressive Property of MSCs Mediated by Cell Surface Receptors |
title_full | Immunosuppressive Property of MSCs Mediated by Cell Surface Receptors |
title_fullStr | Immunosuppressive Property of MSCs Mediated by Cell Surface Receptors |
title_full_unstemmed | Immunosuppressive Property of MSCs Mediated by Cell Surface Receptors |
title_short | Immunosuppressive Property of MSCs Mediated by Cell Surface Receptors |
title_sort | immunosuppressive property of mscs mediated by cell surface receptors |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399134/ https://www.ncbi.nlm.nih.gov/pubmed/32849489 http://dx.doi.org/10.3389/fimmu.2020.01076 |
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