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Notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts
Somatic stem cells hold attractive potential for the treatment of muscular dystrophies (MDs). Mesoangioblasts (MABs) constitute a myogenic subset of muscle pericytes and have been shown to efficiently regenerate dystrophic muscles in mice and dogs. In addition, HLA-matched MABs are currently being t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237240/ https://www.ncbi.nlm.nih.gov/pubmed/25299773 http://dx.doi.org/10.1038/cddis.2014.401 |
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author | Quattrocelli, M Costamagna, D Giacomazzi, G Camps, J Sampaolesi, M |
author_facet | Quattrocelli, M Costamagna, D Giacomazzi, G Camps, J Sampaolesi, M |
author_sort | Quattrocelli, M |
collection | PubMed |
description | Somatic stem cells hold attractive potential for the treatment of muscular dystrophies (MDs). Mesoangioblasts (MABs) constitute a myogenic subset of muscle pericytes and have been shown to efficiently regenerate dystrophic muscles in mice and dogs. In addition, HLA-matched MABs are currently being tested in a phase 1 clinical study on Duchenne MD patients (EudraCT #2011-000176-33). Many reports indicate that the Notch pathway regulates muscle regeneration and satellite cell commitment. However, little is known about Notch-mediated effects on other resident myogenic cells. To possibly potentiate MAB-driven regeneration in vivo, we asked whether Notch signaling played a pivotal role in regulating MAB myogenic capacity. Through different approaches of loss- and gain-of-function in murine and human MABs, we determined that the interplay between Delta-like ligand 1 (Dll1)-activated Notch1 and Mef2C supports MAB commitment in vitro and ameliorates engraftment and functional outcome after intra-arterial delivery in dystrophic mice. Furthermore, using a transgenic mouse model of conditional Dll1 deletion, we demonstrated that Dll1 ablation, either on the injected cells, or on the receiving muscle fibers, impairs MAB regenerative potential. Our data corroborate the perspective of advanced combinations of cell therapy and signaling tuning to enhance therapeutic efficaciousness of somatic stem cells. |
format | Online Article Text |
id | pubmed-4237240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42372402014-11-26 Notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts Quattrocelli, M Costamagna, D Giacomazzi, G Camps, J Sampaolesi, M Cell Death Dis Original Article Somatic stem cells hold attractive potential for the treatment of muscular dystrophies (MDs). Mesoangioblasts (MABs) constitute a myogenic subset of muscle pericytes and have been shown to efficiently regenerate dystrophic muscles in mice and dogs. In addition, HLA-matched MABs are currently being tested in a phase 1 clinical study on Duchenne MD patients (EudraCT #2011-000176-33). Many reports indicate that the Notch pathway regulates muscle regeneration and satellite cell commitment. However, little is known about Notch-mediated effects on other resident myogenic cells. To possibly potentiate MAB-driven regeneration in vivo, we asked whether Notch signaling played a pivotal role in regulating MAB myogenic capacity. Through different approaches of loss- and gain-of-function in murine and human MABs, we determined that the interplay between Delta-like ligand 1 (Dll1)-activated Notch1 and Mef2C supports MAB commitment in vitro and ameliorates engraftment and functional outcome after intra-arterial delivery in dystrophic mice. Furthermore, using a transgenic mouse model of conditional Dll1 deletion, we demonstrated that Dll1 ablation, either on the injected cells, or on the receiving muscle fibers, impairs MAB regenerative potential. Our data corroborate the perspective of advanced combinations of cell therapy and signaling tuning to enhance therapeutic efficaciousness of somatic stem cells. Nature Publishing Group 2014-10 2014-10-09 /pmc/articles/PMC4237240/ /pubmed/25299773 http://dx.doi.org/10.1038/cddis.2014.401 Text en Copyright © 2014 Macmillan Publishers Limited 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 Licence. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons licence, users will need to obtain permission from the licence holder to reproduce the material. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Original Article Quattrocelli, M Costamagna, D Giacomazzi, G Camps, J Sampaolesi, M Notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts |
title | Notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts |
title_full | Notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts |
title_fullStr | Notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts |
title_full_unstemmed | Notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts |
title_short | Notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts |
title_sort | notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237240/ https://www.ncbi.nlm.nih.gov/pubmed/25299773 http://dx.doi.org/10.1038/cddis.2014.401 |
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