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Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension

The prevalence of arterial stiffness and hypertension increases with age. This study investigates the effect of induced pluripotent mesenchymal stem cell-derived extracellular vesicles (EVs) on ageing-associated arterial stiffness and hypertension. EVs were collected and purified from induced plurip...

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Autores principales: Feng, Rui, Ullah, Mujib, Chen, Kai, Ali, Quaisar, Lin, Yi, Sun, Zhongjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480600/
https://www.ncbi.nlm.nih.gov/pubmed/32939234
http://dx.doi.org/10.1080/20013078.2020.1783869
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author Feng, Rui
Ullah, Mujib
Chen, Kai
Ali, Quaisar
Lin, Yi
Sun, Zhongjie
author_facet Feng, Rui
Ullah, Mujib
Chen, Kai
Ali, Quaisar
Lin, Yi
Sun, Zhongjie
author_sort Feng, Rui
collection PubMed
description The prevalence of arterial stiffness and hypertension increases with age. This study investigates the effect of induced pluripotent mesenchymal stem cell-derived extracellular vesicles (EVs) on ageing-associated arterial stiffness and hypertension. EVs were collected and purified from induced pluripotent stem cell-derived mesenchymal stem cells (iPS-MSCs). Young and old male C57BL/6 mice were used. Mice in the EVs group were injected via tail vein once a week for four weeks (18 x 10(6) EVs/mouse/injection). Blood pressure (BP) was measured using the tail-cuff method and validated by direct cannulation. Pulse wave velocity (PWV) was measured using a Doppler workstation. PWV and BP were increased significantly in the old mice, indicating arterial stiffness and hypertension. Intravenous administration of EVs significantly attenuated ageing-related arterial stiffness and hypertension, while enhancing endothelium-dependent vascular relaxation and arterial compliance in the old EVs mice. Elastin degradation and collagen I deposition (fibrosis) were increased in aortas of the old mice, but EVs substantially improved ageing-associated structural remodelling. Mechanistically, EVs abolished downregulation of sirtuin type 1 (SIRT1), and endothelial nitric oxide synthase (eNOS) protein expression in aortas of the older mice. In cultured human aortic endothelial cells, EVs promoted the expression of SIRT1, AMP-activated protein kinase alpha (AMPKα), and eNOS. In conclusion, iPS-MSC-derived EVs attenuated ageing-associated vascular endothelial dysfunction, arterial stiffness, and hypertension, likely via activation of the SIRT1-AMPKα-eNOS pathway and inhibition of MMPs and elastase. Thus, EVs mitigate arterial ageing. This finding also sheds light into the therapeutic potential of EVs for ageing-related vascular diseases. ABBREVIATIONS: EV: Extracellular vesicles; iPS: induced pluripotent stem cell; MSC: mesenchymal stem cell; AMPKα: AMP activated protein kinase α; eNOS: endothelial nitric oxide synthase; Sirt1: sirtuin 1; JNC7: Seventh Report of the Joint National Committee; CVD: cardiovascular disease; PWV: pulse wave velocity; BP: blood pressure; SNP: sodium nitroprusside
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spelling pubmed-74806002020-09-15 Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension Feng, Rui Ullah, Mujib Chen, Kai Ali, Quaisar Lin, Yi Sun, Zhongjie J Extracell Vesicles Research Article The prevalence of arterial stiffness and hypertension increases with age. This study investigates the effect of induced pluripotent mesenchymal stem cell-derived extracellular vesicles (EVs) on ageing-associated arterial stiffness and hypertension. EVs were collected and purified from induced pluripotent stem cell-derived mesenchymal stem cells (iPS-MSCs). Young and old male C57BL/6 mice were used. Mice in the EVs group were injected via tail vein once a week for four weeks (18 x 10(6) EVs/mouse/injection). Blood pressure (BP) was measured using the tail-cuff method and validated by direct cannulation. Pulse wave velocity (PWV) was measured using a Doppler workstation. PWV and BP were increased significantly in the old mice, indicating arterial stiffness and hypertension. Intravenous administration of EVs significantly attenuated ageing-related arterial stiffness and hypertension, while enhancing endothelium-dependent vascular relaxation and arterial compliance in the old EVs mice. Elastin degradation and collagen I deposition (fibrosis) were increased in aortas of the old mice, but EVs substantially improved ageing-associated structural remodelling. Mechanistically, EVs abolished downregulation of sirtuin type 1 (SIRT1), and endothelial nitric oxide synthase (eNOS) protein expression in aortas of the older mice. In cultured human aortic endothelial cells, EVs promoted the expression of SIRT1, AMP-activated protein kinase alpha (AMPKα), and eNOS. In conclusion, iPS-MSC-derived EVs attenuated ageing-associated vascular endothelial dysfunction, arterial stiffness, and hypertension, likely via activation of the SIRT1-AMPKα-eNOS pathway and inhibition of MMPs and elastase. Thus, EVs mitigate arterial ageing. This finding also sheds light into the therapeutic potential of EVs for ageing-related vascular diseases. ABBREVIATIONS: EV: Extracellular vesicles; iPS: induced pluripotent stem cell; MSC: mesenchymal stem cell; AMPKα: AMP activated protein kinase α; eNOS: endothelial nitric oxide synthase; Sirt1: sirtuin 1; JNC7: Seventh Report of the Joint National Committee; CVD: cardiovascular disease; PWV: pulse wave velocity; BP: blood pressure; SNP: sodium nitroprusside Taylor & Francis 2020-06-24 /pmc/articles/PMC7480600/ /pubmed/32939234 http://dx.doi.org/10.1080/20013078.2020.1783869 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of The International Society for Extracellular Vesicles. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Feng, Rui
Ullah, Mujib
Chen, Kai
Ali, Quaisar
Lin, Yi
Sun, Zhongjie
Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension
title Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension
title_full Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension
title_fullStr Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension
title_full_unstemmed Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension
title_short Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension
title_sort stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480600/
https://www.ncbi.nlm.nih.gov/pubmed/32939234
http://dx.doi.org/10.1080/20013078.2020.1783869
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