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Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A

Atherosclerosis is a chronic inflammatory disease associated with the development of plaques that can be converted into an acute clinical event by thrombosis or plaque rupture. Mesenchymal stem cells (MSCs) exhibit therapeutic effects for the treatment of various diseases, including atherosclerosis....

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Autores principales: Yang, Wenzhi, Yin, Ruihua, Zhu, Xiaoyan, Yang, Shaonan, Wang, Jing, Zhou, Zhenfeng, Pan, Xudong, Ma, Aijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732974/
https://www.ncbi.nlm.nih.gov/pubmed/33335797
http://dx.doi.org/10.1016/j.omtn.2020.10.037
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author Yang, Wenzhi
Yin, Ruihua
Zhu, Xiaoyan
Yang, Shaonan
Wang, Jing
Zhou, Zhenfeng
Pan, Xudong
Ma, Aijun
author_facet Yang, Wenzhi
Yin, Ruihua
Zhu, Xiaoyan
Yang, Shaonan
Wang, Jing
Zhou, Zhenfeng
Pan, Xudong
Ma, Aijun
author_sort Yang, Wenzhi
collection PubMed
description Atherosclerosis is a chronic inflammatory disease associated with the development of plaques that can be converted into an acute clinical event by thrombosis or plaque rupture. Mesenchymal stem cells (MSCs) exhibit therapeutic effects for the treatment of various diseases, including atherosclerosis. In this study, we show that microRNA-145 (miR-145) is associated with atherosclerosis by microRNA sequencing and bioinformatics analysis. MSC-derived miR-145-rich exosomes could efficiently deliver miR-145 from MSCs to human umbilical vein endothelial cells (HUVECs). Treatment of miR-145-rich exosomes could downregulate JAM-A, inhibit migration in vitro, and reduce atherosclerotic plaque in vivo. Our study suggests that MSC-derived miR-145-rich exosomes have great potential for atherosclerosis prevention.
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spelling pubmed-77329742020-12-16 Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A Yang, Wenzhi Yin, Ruihua Zhu, Xiaoyan Yang, Shaonan Wang, Jing Zhou, Zhenfeng Pan, Xudong Ma, Aijun Mol Ther Nucleic Acids Original Article Atherosclerosis is a chronic inflammatory disease associated with the development of plaques that can be converted into an acute clinical event by thrombosis or plaque rupture. Mesenchymal stem cells (MSCs) exhibit therapeutic effects for the treatment of various diseases, including atherosclerosis. In this study, we show that microRNA-145 (miR-145) is associated with atherosclerosis by microRNA sequencing and bioinformatics analysis. MSC-derived miR-145-rich exosomes could efficiently deliver miR-145 from MSCs to human umbilical vein endothelial cells (HUVECs). Treatment of miR-145-rich exosomes could downregulate JAM-A, inhibit migration in vitro, and reduce atherosclerotic plaque in vivo. Our study suggests that MSC-derived miR-145-rich exosomes have great potential for atherosclerosis prevention. American Society of Gene & Cell Therapy 2020-11-04 /pmc/articles/PMC7732974/ /pubmed/33335797 http://dx.doi.org/10.1016/j.omtn.2020.10.037 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Yang, Wenzhi
Yin, Ruihua
Zhu, Xiaoyan
Yang, Shaonan
Wang, Jing
Zhou, Zhenfeng
Pan, Xudong
Ma, Aijun
Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A
title Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A
title_full Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A
title_fullStr Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A
title_full_unstemmed Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A
title_short Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A
title_sort mesenchymal stem-cell-derived exosomal mir-145 inhibits atherosclerosis by targeting jam-a
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732974/
https://www.ncbi.nlm.nih.gov/pubmed/33335797
http://dx.doi.org/10.1016/j.omtn.2020.10.037
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