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Cargo proteins in extracellular vesicles: potential for novel therapeutics in non-alcoholic steatohepatitis
BACKGROUND: Extracellular vesicles (EVs) are recognized as novel cell-free therapeutics. Non-alcoholic steatohepatitis (NASH) remains a critical health problem. Herein, we show that EVs from pan peroxisome proliferator-activated receptor agonist-primed induced mesenchymal stem cell (pan PPAR-iMSC-EV...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600817/ https://www.ncbi.nlm.nih.gov/pubmed/34789265 http://dx.doi.org/10.1186/s12951-021-01120-y |
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author | Kim, Jimin Lee, Seul Ki Jeong, Seon-Yeong Cho, Hye Jin Park, Joonghoon Kim, Tae Min Kim, Soo |
author_facet | Kim, Jimin Lee, Seul Ki Jeong, Seon-Yeong Cho, Hye Jin Park, Joonghoon Kim, Tae Min Kim, Soo |
author_sort | Kim, Jimin |
collection | PubMed |
description | BACKGROUND: Extracellular vesicles (EVs) are recognized as novel cell-free therapeutics. Non-alcoholic steatohepatitis (NASH) remains a critical health problem. Herein, we show that EVs from pan peroxisome proliferator-activated receptor agonist-primed induced mesenchymal stem cell (pan PPAR-iMSC-EVs) has unique cargo protein signatures, and demonstrate its therapeutic function in NASH. RESULTS: A unique protein signatures were identified in pan PPAR-iMSC-EVs against those from non-stimulated iMSC-EVs. NASH mice receiving pan PPAR-iMSC-EVs showed reduced steatotic changes and ameliorated ER stress and mitochondiral oxidative stress induced by inflammation. Moreover, pan PPAR-iMSC-EVs promoted liver regeneration via inhibiting apoptosis and enhancing proliferation. CONCLUSIONS: We conclude that our strategy for enriching unique cargo proteins in EVs may facilitate the development of novel therapeutic option for NASH. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01120-y. |
format | Online Article Text |
id | pubmed-8600817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86008172021-11-19 Cargo proteins in extracellular vesicles: potential for novel therapeutics in non-alcoholic steatohepatitis Kim, Jimin Lee, Seul Ki Jeong, Seon-Yeong Cho, Hye Jin Park, Joonghoon Kim, Tae Min Kim, Soo J Nanobiotechnology Research BACKGROUND: Extracellular vesicles (EVs) are recognized as novel cell-free therapeutics. Non-alcoholic steatohepatitis (NASH) remains a critical health problem. Herein, we show that EVs from pan peroxisome proliferator-activated receptor agonist-primed induced mesenchymal stem cell (pan PPAR-iMSC-EVs) has unique cargo protein signatures, and demonstrate its therapeutic function in NASH. RESULTS: A unique protein signatures were identified in pan PPAR-iMSC-EVs against those from non-stimulated iMSC-EVs. NASH mice receiving pan PPAR-iMSC-EVs showed reduced steatotic changes and ameliorated ER stress and mitochondiral oxidative stress induced by inflammation. Moreover, pan PPAR-iMSC-EVs promoted liver regeneration via inhibiting apoptosis and enhancing proliferation. CONCLUSIONS: We conclude that our strategy for enriching unique cargo proteins in EVs may facilitate the development of novel therapeutic option for NASH. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01120-y. BioMed Central 2021-11-17 /pmc/articles/PMC8600817/ /pubmed/34789265 http://dx.doi.org/10.1186/s12951-021-01120-y Text en © The Author(s) 2021 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 | Research Kim, Jimin Lee, Seul Ki Jeong, Seon-Yeong Cho, Hye Jin Park, Joonghoon Kim, Tae Min Kim, Soo Cargo proteins in extracellular vesicles: potential for novel therapeutics in non-alcoholic steatohepatitis |
title | Cargo proteins in extracellular vesicles: potential for novel therapeutics in non-alcoholic steatohepatitis |
title_full | Cargo proteins in extracellular vesicles: potential for novel therapeutics in non-alcoholic steatohepatitis |
title_fullStr | Cargo proteins in extracellular vesicles: potential for novel therapeutics in non-alcoholic steatohepatitis |
title_full_unstemmed | Cargo proteins in extracellular vesicles: potential for novel therapeutics in non-alcoholic steatohepatitis |
title_short | Cargo proteins in extracellular vesicles: potential for novel therapeutics in non-alcoholic steatohepatitis |
title_sort | cargo proteins in extracellular vesicles: potential for novel therapeutics in non-alcoholic steatohepatitis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600817/ https://www.ncbi.nlm.nih.gov/pubmed/34789265 http://dx.doi.org/10.1186/s12951-021-01120-y |
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