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Exosomes Immunity Strategy: A Novel Approach for Ameliorating Intervertebral Disc Degeneration
Low back pain (LBP), which is one of the most severe medical and social problems globally, has affected nearly 80% of the population worldwide, and intervertebral disc degeneration (IDD) is a common musculoskeletal disorder that happens to be the primary trigger of LBP. The pathology of IDD is based...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870130/ https://www.ncbi.nlm.nih.gov/pubmed/35223870 http://dx.doi.org/10.3389/fcell.2021.822149 |
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author | Li, Weihang Zhang, Shilei Wang, Dong Zhang, Huan Shi, Quan Zhang, Yuyuan Wang, Mo Ding, Ziyi Xu, Songjie Gao, Bo Yan, Ming |
author_facet | Li, Weihang Zhang, Shilei Wang, Dong Zhang, Huan Shi, Quan Zhang, Yuyuan Wang, Mo Ding, Ziyi Xu, Songjie Gao, Bo Yan, Ming |
author_sort | Li, Weihang |
collection | PubMed |
description | Low back pain (LBP), which is one of the most severe medical and social problems globally, has affected nearly 80% of the population worldwide, and intervertebral disc degeneration (IDD) is a common musculoskeletal disorder that happens to be the primary trigger of LBP. The pathology of IDD is based on the impaired homeostasis of catabolism and anabolism in the extracellular matrix (ECM), uncontrolled activation of immunologic cascades, dysfunction, and loss of nucleus pulposus (NP) cells in addition to dynamic cellular and biochemical alterations in the microenvironment of intervertebral disc (IVD). Currently, the main therapeutic approach regarding IDD is surgical intervention, but it could not considerably cure IDD. Exosomes, extracellular vesicles with a diameter of 30–150 nm, are secreted by various kinds of cell types like stem cells, tumor cells, immune cells, and endothelial cells; the lipid bilayer of the exosomes protects them from ribonuclease degradation and helps improve their biological efficiency in recipient cells. Increasing lines of evidence have reported the promising applications of exosomes in immunological diseases, and regarded exosomes as a potential therapeutic source for IDD. This review focuses on clarifying novel therapies based on exosomes derived from different cell sources and the essential roles of exosomes in regulating IDD, especially the immunologic strategy. |
format | Online Article Text |
id | pubmed-8870130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88701302022-02-25 Exosomes Immunity Strategy: A Novel Approach for Ameliorating Intervertebral Disc Degeneration Li, Weihang Zhang, Shilei Wang, Dong Zhang, Huan Shi, Quan Zhang, Yuyuan Wang, Mo Ding, Ziyi Xu, Songjie Gao, Bo Yan, Ming Front Cell Dev Biol Cell and Developmental Biology Low back pain (LBP), which is one of the most severe medical and social problems globally, has affected nearly 80% of the population worldwide, and intervertebral disc degeneration (IDD) is a common musculoskeletal disorder that happens to be the primary trigger of LBP. The pathology of IDD is based on the impaired homeostasis of catabolism and anabolism in the extracellular matrix (ECM), uncontrolled activation of immunologic cascades, dysfunction, and loss of nucleus pulposus (NP) cells in addition to dynamic cellular and biochemical alterations in the microenvironment of intervertebral disc (IVD). Currently, the main therapeutic approach regarding IDD is surgical intervention, but it could not considerably cure IDD. Exosomes, extracellular vesicles with a diameter of 30–150 nm, are secreted by various kinds of cell types like stem cells, tumor cells, immune cells, and endothelial cells; the lipid bilayer of the exosomes protects them from ribonuclease degradation and helps improve their biological efficiency in recipient cells. Increasing lines of evidence have reported the promising applications of exosomes in immunological diseases, and regarded exosomes as a potential therapeutic source for IDD. This review focuses on clarifying novel therapies based on exosomes derived from different cell sources and the essential roles of exosomes in regulating IDD, especially the immunologic strategy. Frontiers Media S.A. 2022-02-10 /pmc/articles/PMC8870130/ /pubmed/35223870 http://dx.doi.org/10.3389/fcell.2021.822149 Text en Copyright © 2022 Li, Zhang, Wang, Zhang, Shi, Zhang, Wang, Ding, Xu, Gao and Yan. https://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 | Cell and Developmental Biology Li, Weihang Zhang, Shilei Wang, Dong Zhang, Huan Shi, Quan Zhang, Yuyuan Wang, Mo Ding, Ziyi Xu, Songjie Gao, Bo Yan, Ming Exosomes Immunity Strategy: A Novel Approach for Ameliorating Intervertebral Disc Degeneration |
title | Exosomes Immunity Strategy: A Novel Approach for Ameliorating Intervertebral Disc Degeneration |
title_full | Exosomes Immunity Strategy: A Novel Approach for Ameliorating Intervertebral Disc Degeneration |
title_fullStr | Exosomes Immunity Strategy: A Novel Approach for Ameliorating Intervertebral Disc Degeneration |
title_full_unstemmed | Exosomes Immunity Strategy: A Novel Approach for Ameliorating Intervertebral Disc Degeneration |
title_short | Exosomes Immunity Strategy: A Novel Approach for Ameliorating Intervertebral Disc Degeneration |
title_sort | exosomes immunity strategy: a novel approach for ameliorating intervertebral disc degeneration |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870130/ https://www.ncbi.nlm.nih.gov/pubmed/35223870 http://dx.doi.org/10.3389/fcell.2021.822149 |
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