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Apoptotic Cell-Derived Extracellular Vesicles: More Than Just Debris
The many functions of extracellular vesicles (EVs) like exosomes and microvesicles released from healthy cells have been well characterized, particularly in relation to their roles in immune modulation. Apoptotic bodies, a major class of EV released as a product of apoptotic cell disassembly, and ot...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031707/ https://www.ncbi.nlm.nih.gov/pubmed/30002658 http://dx.doi.org/10.3389/fimmu.2018.01486 |
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author | Caruso, Sarah Poon, Ivan K. H. |
author_facet | Caruso, Sarah Poon, Ivan K. H. |
author_sort | Caruso, Sarah |
collection | PubMed |
description | The many functions of extracellular vesicles (EVs) like exosomes and microvesicles released from healthy cells have been well characterized, particularly in relation to their roles in immune modulation. Apoptotic bodies, a major class of EV released as a product of apoptotic cell disassembly, and other types of EVs released from dying cells are also becoming recognized as key players in this emerging field. There is now increasing evidence to suggest that EVs produced during apoptosis have important immune regulatory roles, a concept relevant across different disease settings including autoimmunity, cancer, and infection. Therefore, this review focuses on how the formation of EVs during apoptosis could be a key mechanism of immune modulation by dying cells. |
format | Online Article Text |
id | pubmed-6031707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60317072018-07-12 Apoptotic Cell-Derived Extracellular Vesicles: More Than Just Debris Caruso, Sarah Poon, Ivan K. H. Front Immunol Immunology The many functions of extracellular vesicles (EVs) like exosomes and microvesicles released from healthy cells have been well characterized, particularly in relation to their roles in immune modulation. Apoptotic bodies, a major class of EV released as a product of apoptotic cell disassembly, and other types of EVs released from dying cells are also becoming recognized as key players in this emerging field. There is now increasing evidence to suggest that EVs produced during apoptosis have important immune regulatory roles, a concept relevant across different disease settings including autoimmunity, cancer, and infection. Therefore, this review focuses on how the formation of EVs during apoptosis could be a key mechanism of immune modulation by dying cells. Frontiers Media S.A. 2018-06-28 /pmc/articles/PMC6031707/ /pubmed/30002658 http://dx.doi.org/10.3389/fimmu.2018.01486 Text en Copyright © 2018 Caruso and Poon. 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 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 Caruso, Sarah Poon, Ivan K. H. Apoptotic Cell-Derived Extracellular Vesicles: More Than Just Debris |
title | Apoptotic Cell-Derived Extracellular Vesicles: More Than Just Debris |
title_full | Apoptotic Cell-Derived Extracellular Vesicles: More Than Just Debris |
title_fullStr | Apoptotic Cell-Derived Extracellular Vesicles: More Than Just Debris |
title_full_unstemmed | Apoptotic Cell-Derived Extracellular Vesicles: More Than Just Debris |
title_short | Apoptotic Cell-Derived Extracellular Vesicles: More Than Just Debris |
title_sort | apoptotic cell-derived extracellular vesicles: more than just debris |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031707/ https://www.ncbi.nlm.nih.gov/pubmed/30002658 http://dx.doi.org/10.3389/fimmu.2018.01486 |
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