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Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing
Extracellular vesicles (EVs), comprising microvesicles (MVs) and exosomes (Exos), are membranous vesicles secreted by cells which mediate the repair of cellular and tissue damage via paracrine mechanisms. The action of EVs under normative and morbid conditions in the context of ageing remains largel...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340655/ https://www.ncbi.nlm.nih.gov/pubmed/37443741 http://dx.doi.org/10.3390/cells12131707 |
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author | Panagiotou, Nikolaos McGuinness, Dagmara Jaminon, Armand M. G. Mees, Barend Selman, Colin Schurgers, Leon Shiels, Paul G. |
author_facet | Panagiotou, Nikolaos McGuinness, Dagmara Jaminon, Armand M. G. Mees, Barend Selman, Colin Schurgers, Leon Shiels, Paul G. |
author_sort | Panagiotou, Nikolaos |
collection | PubMed |
description | Extracellular vesicles (EVs), comprising microvesicles (MVs) and exosomes (Exos), are membranous vesicles secreted by cells which mediate the repair of cellular and tissue damage via paracrine mechanisms. The action of EVs under normative and morbid conditions in the context of ageing remains largely unexplored. We demonstrate that MVs, but not Exos, from Pathfinder cells (PCs), a putative stem cell regulatory cell type, enhance the repair of human dermal fibroblast (HDF) and mesenchymal stem cell (MSC) co-cultures, following both mechanical and genotoxic stress. Critically, this effect was found to be both cellular age and stress specific. Notably, MV treatment was unable to repair mechanical injury in older co-cultures but remained therapeutic following genotoxic stress. These observations were further confirmed in human dermal fibroblast (HDF) and vascular smooth muscle cell (VSMC) co-cultures of increasing cellular age. In a model of comorbidity comprising co-cultures of HDFs and highly senescent abdominal aortic aneurysm (AAA) VSMCs, MV administration appeared to be senotherapeutic, following both mechanical and genotoxic stress. Our data provide insights into EVs and the specific roles they play during tissue repair and ageing. These data will potentiate the development of novel cell-free therapeutic interventions capable of attenuating age-associated morbidities and avoiding undesired effects. |
format | Online Article Text |
id | pubmed-10340655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103406552023-07-14 Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing Panagiotou, Nikolaos McGuinness, Dagmara Jaminon, Armand M. G. Mees, Barend Selman, Colin Schurgers, Leon Shiels, Paul G. Cells Article Extracellular vesicles (EVs), comprising microvesicles (MVs) and exosomes (Exos), are membranous vesicles secreted by cells which mediate the repair of cellular and tissue damage via paracrine mechanisms. The action of EVs under normative and morbid conditions in the context of ageing remains largely unexplored. We demonstrate that MVs, but not Exos, from Pathfinder cells (PCs), a putative stem cell regulatory cell type, enhance the repair of human dermal fibroblast (HDF) and mesenchymal stem cell (MSC) co-cultures, following both mechanical and genotoxic stress. Critically, this effect was found to be both cellular age and stress specific. Notably, MV treatment was unable to repair mechanical injury in older co-cultures but remained therapeutic following genotoxic stress. These observations were further confirmed in human dermal fibroblast (HDF) and vascular smooth muscle cell (VSMC) co-cultures of increasing cellular age. In a model of comorbidity comprising co-cultures of HDFs and highly senescent abdominal aortic aneurysm (AAA) VSMCs, MV administration appeared to be senotherapeutic, following both mechanical and genotoxic stress. Our data provide insights into EVs and the specific roles they play during tissue repair and ageing. These data will potentiate the development of novel cell-free therapeutic interventions capable of attenuating age-associated morbidities and avoiding undesired effects. MDPI 2023-06-23 /pmc/articles/PMC10340655/ /pubmed/37443741 http://dx.doi.org/10.3390/cells12131707 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Panagiotou, Nikolaos McGuinness, Dagmara Jaminon, Armand M. G. Mees, Barend Selman, Colin Schurgers, Leon Shiels, Paul G. Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing |
title | Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing |
title_full | Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing |
title_fullStr | Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing |
title_full_unstemmed | Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing |
title_short | Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing |
title_sort | microvesicle-mediated tissue regeneration mitigates the effects of cellular ageing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340655/ https://www.ncbi.nlm.nih.gov/pubmed/37443741 http://dx.doi.org/10.3390/cells12131707 |
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