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Extracellular Vesicles in Musculoskeletal Pathologies and Regeneration
The incidence of musculoskeletal diseases is steadily increasing with aging of the population. In the past years, extracellular vesicles (EVs) have gained attention in musculoskeletal research. EVs have been associated with various musculoskeletal pathologies as well as suggested as treatment option...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7855463/ https://www.ncbi.nlm.nih.gov/pubmed/33553127 http://dx.doi.org/10.3389/fbioe.2020.624096 |
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author | Herrmann, Marietta Diederichs, Solvig Melnik, Svitlana Riegger, Jana Trivanović, Drenka Li, Shushan Jenei-Lanzl, Zsuzsa Brenner, Rolf E. Huber-Lang, Markus Zaucke, Frank Schildberg, Frank A. Grässel, Susanne |
author_facet | Herrmann, Marietta Diederichs, Solvig Melnik, Svitlana Riegger, Jana Trivanović, Drenka Li, Shushan Jenei-Lanzl, Zsuzsa Brenner, Rolf E. Huber-Lang, Markus Zaucke, Frank Schildberg, Frank A. Grässel, Susanne |
author_sort | Herrmann, Marietta |
collection | PubMed |
description | The incidence of musculoskeletal diseases is steadily increasing with aging of the population. In the past years, extracellular vesicles (EVs) have gained attention in musculoskeletal research. EVs have been associated with various musculoskeletal pathologies as well as suggested as treatment option. EVs play a pivotal role in communication between cells and their environment. Thereby, the EV cargo is highly dependent on their cellular origin. In this review, we summarize putative mechanisms by which EVs can contribute to musculoskeletal tissue homeostasis, regeneration and disease, in particular matrix remodeling and mineralization, pro-angiogenic effects and immunomodulatory activities. Mesenchymal stromal cells (MSCs) present the most frequently used cell source for EV generation for musculoskeletal applications, and herein we discuss how the MSC phenotype can influence the cargo and thus the regenerative potential of EVs. Induced pluripotent stem cell-derived mesenchymal progenitor cells (iMPs) may overcome current limitations of MSCs, and iMP-derived EVs are discussed as an alternative strategy. In the last part of the article, we focus on therapeutic applications of EVs and discuss both practical considerations for EV production and the current state of EV-based therapies. |
format | Online Article Text |
id | pubmed-7855463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78554632021-02-04 Extracellular Vesicles in Musculoskeletal Pathologies and Regeneration Herrmann, Marietta Diederichs, Solvig Melnik, Svitlana Riegger, Jana Trivanović, Drenka Li, Shushan Jenei-Lanzl, Zsuzsa Brenner, Rolf E. Huber-Lang, Markus Zaucke, Frank Schildberg, Frank A. Grässel, Susanne Front Bioeng Biotechnol Bioengineering and Biotechnology The incidence of musculoskeletal diseases is steadily increasing with aging of the population. In the past years, extracellular vesicles (EVs) have gained attention in musculoskeletal research. EVs have been associated with various musculoskeletal pathologies as well as suggested as treatment option. EVs play a pivotal role in communication between cells and their environment. Thereby, the EV cargo is highly dependent on their cellular origin. In this review, we summarize putative mechanisms by which EVs can contribute to musculoskeletal tissue homeostasis, regeneration and disease, in particular matrix remodeling and mineralization, pro-angiogenic effects and immunomodulatory activities. Mesenchymal stromal cells (MSCs) present the most frequently used cell source for EV generation for musculoskeletal applications, and herein we discuss how the MSC phenotype can influence the cargo and thus the regenerative potential of EVs. Induced pluripotent stem cell-derived mesenchymal progenitor cells (iMPs) may overcome current limitations of MSCs, and iMP-derived EVs are discussed as an alternative strategy. In the last part of the article, we focus on therapeutic applications of EVs and discuss both practical considerations for EV production and the current state of EV-based therapies. Frontiers Media S.A. 2021-01-20 /pmc/articles/PMC7855463/ /pubmed/33553127 http://dx.doi.org/10.3389/fbioe.2020.624096 Text en Copyright © 2021 Herrmann, Diederichs, Melnik, Riegger, Trivanović, Li, Jenei-Lanzl, Brenner, Huber-Lang, Zaucke, Schildberg and Grässel. 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 | Bioengineering and Biotechnology Herrmann, Marietta Diederichs, Solvig Melnik, Svitlana Riegger, Jana Trivanović, Drenka Li, Shushan Jenei-Lanzl, Zsuzsa Brenner, Rolf E. Huber-Lang, Markus Zaucke, Frank Schildberg, Frank A. Grässel, Susanne Extracellular Vesicles in Musculoskeletal Pathologies and Regeneration |
title | Extracellular Vesicles in Musculoskeletal Pathologies and Regeneration |
title_full | Extracellular Vesicles in Musculoskeletal Pathologies and Regeneration |
title_fullStr | Extracellular Vesicles in Musculoskeletal Pathologies and Regeneration |
title_full_unstemmed | Extracellular Vesicles in Musculoskeletal Pathologies and Regeneration |
title_short | Extracellular Vesicles in Musculoskeletal Pathologies and Regeneration |
title_sort | extracellular vesicles in musculoskeletal pathologies and regeneration |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7855463/ https://www.ncbi.nlm.nih.gov/pubmed/33553127 http://dx.doi.org/10.3389/fbioe.2020.624096 |
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