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Ex vivo Induction of Apoptotic Mesenchymal Stem Cell by High Hydrostatic Pressure
Among promising solutions for tissue repair and wound healing, mesenchymal stem (or stromal) cells (MSCs) have been a focus of attention and have become the most clinically studied experimental cell therapy. Recent studies reported the importance of apoptosis in MSC-mediated immunomodulation, in whi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036216/ https://www.ncbi.nlm.nih.gov/pubmed/33128169 http://dx.doi.org/10.1007/s12015-020-10071-0 |
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author | Le, Tien Minh Morimoto, Naoki Ly, Nhung Thi My Mitsui, Toshihito Notodihardjo, Sharon Claudia Ogino, Shuichi Arata, Jun Kakudo, Natsuko Kusumoto, Kenji |
author_facet | Le, Tien Minh Morimoto, Naoki Ly, Nhung Thi My Mitsui, Toshihito Notodihardjo, Sharon Claudia Ogino, Shuichi Arata, Jun Kakudo, Natsuko Kusumoto, Kenji |
author_sort | Le, Tien Minh |
collection | PubMed |
description | Among promising solutions for tissue repair and wound healing, mesenchymal stem (or stromal) cells (MSCs) have been a focus of attention and have become the most clinically studied experimental cell therapy. Recent studies reported the importance of apoptosis in MSC-mediated immunomodulation, in which apoptotic MSCs (apoMSCs) were shown to be superior to living MSCs. Nowadays, high hydrostatic pressure (HHP), a physical technique that uses only fluid pressure, has been developed and applied in various bioscience fields, including biotechnology, biomaterials, and regenerative medicine, as its safe and simply operation. In the current study, we investigated the impact of HHP treatment on human bone marrow-MSC survival and proliferation. Based on the detection of executioner caspase activation, phosphatidylserine exposure, DNA fragmentation (TUNEL) and irrefutable ultrastructural morphological changes on transmission electron microscopy (TEM), our data revealed that HHP treatment induced complete apoptosis in MSCs. Notably, this technique might provide manipulated products for use in cell-based therapies as manufacturing capability expands. We hope that our findings will contribute to the improvement of MSCs or EVs in translational research development. [Figure: see text] |
format | Online Article Text |
id | pubmed-8036216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-80362162021-04-27 Ex vivo Induction of Apoptotic Mesenchymal Stem Cell by High Hydrostatic Pressure Le, Tien Minh Morimoto, Naoki Ly, Nhung Thi My Mitsui, Toshihito Notodihardjo, Sharon Claudia Ogino, Shuichi Arata, Jun Kakudo, Natsuko Kusumoto, Kenji Stem Cell Rev Rep Article Among promising solutions for tissue repair and wound healing, mesenchymal stem (or stromal) cells (MSCs) have been a focus of attention and have become the most clinically studied experimental cell therapy. Recent studies reported the importance of apoptosis in MSC-mediated immunomodulation, in which apoptotic MSCs (apoMSCs) were shown to be superior to living MSCs. Nowadays, high hydrostatic pressure (HHP), a physical technique that uses only fluid pressure, has been developed and applied in various bioscience fields, including biotechnology, biomaterials, and regenerative medicine, as its safe and simply operation. In the current study, we investigated the impact of HHP treatment on human bone marrow-MSC survival and proliferation. Based on the detection of executioner caspase activation, phosphatidylserine exposure, DNA fragmentation (TUNEL) and irrefutable ultrastructural morphological changes on transmission electron microscopy (TEM), our data revealed that HHP treatment induced complete apoptosis in MSCs. Notably, this technique might provide manipulated products for use in cell-based therapies as manufacturing capability expands. We hope that our findings will contribute to the improvement of MSCs or EVs in translational research development. [Figure: see text] Springer US 2020-10-31 2021 /pmc/articles/PMC8036216/ /pubmed/33128169 http://dx.doi.org/10.1007/s12015-020-10071-0 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Le, Tien Minh Morimoto, Naoki Ly, Nhung Thi My Mitsui, Toshihito Notodihardjo, Sharon Claudia Ogino, Shuichi Arata, Jun Kakudo, Natsuko Kusumoto, Kenji Ex vivo Induction of Apoptotic Mesenchymal Stem Cell by High Hydrostatic Pressure |
title | Ex vivo Induction of Apoptotic Mesenchymal Stem Cell by High Hydrostatic Pressure |
title_full | Ex vivo Induction of Apoptotic Mesenchymal Stem Cell by High Hydrostatic Pressure |
title_fullStr | Ex vivo Induction of Apoptotic Mesenchymal Stem Cell by High Hydrostatic Pressure |
title_full_unstemmed | Ex vivo Induction of Apoptotic Mesenchymal Stem Cell by High Hydrostatic Pressure |
title_short | Ex vivo Induction of Apoptotic Mesenchymal Stem Cell by High Hydrostatic Pressure |
title_sort | ex vivo induction of apoptotic mesenchymal stem cell by high hydrostatic pressure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036216/ https://www.ncbi.nlm.nih.gov/pubmed/33128169 http://dx.doi.org/10.1007/s12015-020-10071-0 |
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