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Notch activation enhances mesenchymal stem cell sheet osteogenic potential by inhibition of cellular senescence
Our previous studies have confirmed the therapeutic effects of mesenchymal stem cell (MSC) monolayer sheet transplantation on allograft repair. A limiting factor in their application is the loss of MSC multi-potency as a result of high density sheet culture-induced senescence. In the study reported...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386477/ https://www.ncbi.nlm.nih.gov/pubmed/28151468 http://dx.doi.org/10.1038/cddis.2017.2 |
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author | Tian, Ye Xu, Ying Xue, Taiyang Chen, Longgang Shi, Bin Shu, Bing Xie, Chao Max Morandi, Massimo Jaeblon, Todd Marymont, John V Dong, Yufeng |
author_facet | Tian, Ye Xu, Ying Xue, Taiyang Chen, Longgang Shi, Bin Shu, Bing Xie, Chao Max Morandi, Massimo Jaeblon, Todd Marymont, John V Dong, Yufeng |
author_sort | Tian, Ye |
collection | PubMed |
description | Our previous studies have confirmed the therapeutic effects of mesenchymal stem cell (MSC) monolayer sheet transplantation on allograft repair. A limiting factor in their application is the loss of MSC multi-potency as a result of high density sheet culture-induced senescence. In the study reported in this article, we tested whether Notch activation could be used to prevent or delay sheet culture-induced cell aging. Our results showed that, during in vitro long-term (5-day) cell sheet culture, MSCs progressively lose their progenitor characteristics. In contrast, Notch activation by Jagged1 in MSC sheet culture showed reduced cellular senescence and cell cycle arrest compared with control MSCs without Notch activation. Importantly, knockdown of Notch target gene Hes1 totally blocked the inhibition effect of Jagged1 on cellular senescence. Finally, the in vivo allograft transplantation data showed a significant enhanced callus formation and biomechanical properties in Notch activation cultured long-term sheet groups when compared with long-term cultured sheet without Notch activation. Our results suggest that Notch activation by Jagged1 could be used to overcome the stem cell aging caused by high density sheet culture, thereby increasing the therapeutic potential of MSC sheets for tissue regeneration. |
format | Online Article Text |
id | pubmed-5386477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53864772017-04-26 Notch activation enhances mesenchymal stem cell sheet osteogenic potential by inhibition of cellular senescence Tian, Ye Xu, Ying Xue, Taiyang Chen, Longgang Shi, Bin Shu, Bing Xie, Chao Max Morandi, Massimo Jaeblon, Todd Marymont, John V Dong, Yufeng Cell Death Dis Original Article Our previous studies have confirmed the therapeutic effects of mesenchymal stem cell (MSC) monolayer sheet transplantation on allograft repair. A limiting factor in their application is the loss of MSC multi-potency as a result of high density sheet culture-induced senescence. In the study reported in this article, we tested whether Notch activation could be used to prevent or delay sheet culture-induced cell aging. Our results showed that, during in vitro long-term (5-day) cell sheet culture, MSCs progressively lose their progenitor characteristics. In contrast, Notch activation by Jagged1 in MSC sheet culture showed reduced cellular senescence and cell cycle arrest compared with control MSCs without Notch activation. Importantly, knockdown of Notch target gene Hes1 totally blocked the inhibition effect of Jagged1 on cellular senescence. Finally, the in vivo allograft transplantation data showed a significant enhanced callus formation and biomechanical properties in Notch activation cultured long-term sheet groups when compared with long-term cultured sheet without Notch activation. Our results suggest that Notch activation by Jagged1 could be used to overcome the stem cell aging caused by high density sheet culture, thereby increasing the therapeutic potential of MSC sheets for tissue regeneration. Nature Publishing Group 2017-02 2017-02-02 /pmc/articles/PMC5386477/ /pubmed/28151468 http://dx.doi.org/10.1038/cddis.2017.2 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Tian, Ye Xu, Ying Xue, Taiyang Chen, Longgang Shi, Bin Shu, Bing Xie, Chao Max Morandi, Massimo Jaeblon, Todd Marymont, John V Dong, Yufeng Notch activation enhances mesenchymal stem cell sheet osteogenic potential by inhibition of cellular senescence |
title | Notch activation enhances mesenchymal stem cell sheet osteogenic potential by inhibition of cellular senescence |
title_full | Notch activation enhances mesenchymal stem cell sheet osteogenic potential by inhibition of cellular senescence |
title_fullStr | Notch activation enhances mesenchymal stem cell sheet osteogenic potential by inhibition of cellular senescence |
title_full_unstemmed | Notch activation enhances mesenchymal stem cell sheet osteogenic potential by inhibition of cellular senescence |
title_short | Notch activation enhances mesenchymal stem cell sheet osteogenic potential by inhibition of cellular senescence |
title_sort | notch activation enhances mesenchymal stem cell sheet osteogenic potential by inhibition of cellular senescence |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386477/ https://www.ncbi.nlm.nih.gov/pubmed/28151468 http://dx.doi.org/10.1038/cddis.2017.2 |
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