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Extracellular vesicles and COPD: foe or friend?
Chronic obstructive pulmonary disease (COPD) is a chronic inflammatory airway disease characterized by progressive airflow limitation. The complex biological processes of COPD include protein hydrolysis tissue remodeling, innate immune inflammation, disturbed host-pathogen response, abnormal cellula...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161449/ https://www.ncbi.nlm.nih.gov/pubmed/37147634 http://dx.doi.org/10.1186/s12951-023-01911-5 |
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author | Wu, Jiankang Ma, Yiming Chen, Yan |
author_facet | Wu, Jiankang Ma, Yiming Chen, Yan |
author_sort | Wu, Jiankang |
collection | PubMed |
description | Chronic obstructive pulmonary disease (COPD) is a chronic inflammatory airway disease characterized by progressive airflow limitation. The complex biological processes of COPD include protein hydrolysis tissue remodeling, innate immune inflammation, disturbed host-pathogen response, abnormal cellular phenotype conversion, and cellular senescence. Extracellular vesicles (EVs) (including apoptotic vesicles, microvesicles and exosomes), are released by almost all cell types and can be found in a variety of body fluids including blood, sputum and urine. EVs are key mediators in cell-cell communication and can be used by using their bioactive substances (DNA, RNA, miRNA, proteins and other metabolites) to enable cells in adjacent and distant tissues to perform a wide variety of functions, which in turn affect the physiological and pathological functions of the body. Thus, EVs is expected to play an important role in the pathogenesis of COPD, which in turn affects its acute exacerbations and may serve as a diagnostic marker for it. Furthermore, recent therapeutic approaches and advances have introduced EVs into the treatment of COPD, such as the modification of EVs into novel drug delivery vehicles. Here, we discuss the role of EVs from cells of different origins in the pathogenesis of COPD and explore their possible use as biomarkers in diagnosis, and finally describe their role in therapy and future prospects for their application. [Figure: see text] |
format | Online Article Text |
id | pubmed-10161449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101614492023-05-06 Extracellular vesicles and COPD: foe or friend? Wu, Jiankang Ma, Yiming Chen, Yan J Nanobiotechnology Review Chronic obstructive pulmonary disease (COPD) is a chronic inflammatory airway disease characterized by progressive airflow limitation. The complex biological processes of COPD include protein hydrolysis tissue remodeling, innate immune inflammation, disturbed host-pathogen response, abnormal cellular phenotype conversion, and cellular senescence. Extracellular vesicles (EVs) (including apoptotic vesicles, microvesicles and exosomes), are released by almost all cell types and can be found in a variety of body fluids including blood, sputum and urine. EVs are key mediators in cell-cell communication and can be used by using their bioactive substances (DNA, RNA, miRNA, proteins and other metabolites) to enable cells in adjacent and distant tissues to perform a wide variety of functions, which in turn affect the physiological and pathological functions of the body. Thus, EVs is expected to play an important role in the pathogenesis of COPD, which in turn affects its acute exacerbations and may serve as a diagnostic marker for it. Furthermore, recent therapeutic approaches and advances have introduced EVs into the treatment of COPD, such as the modification of EVs into novel drug delivery vehicles. Here, we discuss the role of EVs from cells of different origins in the pathogenesis of COPD and explore their possible use as biomarkers in diagnosis, and finally describe their role in therapy and future prospects for their application. [Figure: see text] BioMed Central 2023-05-05 /pmc/articles/PMC10161449/ /pubmed/37147634 http://dx.doi.org/10.1186/s12951-023-01911-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Wu, Jiankang Ma, Yiming Chen, Yan Extracellular vesicles and COPD: foe or friend? |
title | Extracellular vesicles and COPD: foe or friend? |
title_full | Extracellular vesicles and COPD: foe or friend? |
title_fullStr | Extracellular vesicles and COPD: foe or friend? |
title_full_unstemmed | Extracellular vesicles and COPD: foe or friend? |
title_short | Extracellular vesicles and COPD: foe or friend? |
title_sort | extracellular vesicles and copd: foe or friend? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161449/ https://www.ncbi.nlm.nih.gov/pubmed/37147634 http://dx.doi.org/10.1186/s12951-023-01911-5 |
work_keys_str_mv | AT wujiankang extracellularvesiclesandcopdfoeorfriend AT mayiming extracellularvesiclesandcopdfoeorfriend AT chenyan extracellularvesiclesandcopdfoeorfriend |