TY - JOUR
T1 - Notch signaling regulates myogenic regenerative capacity of murine and human mesoangioblasts
AU - Quattrocelli, Mattia
AU - Costamagna, D.
AU - Giacomazzi, G.
AU - Camps, J.
AU - Sampaolesi, M.
N1 - Funding Information:
Acknowledgements. We are grateful to Professor Winoto (University of Berkeley, CA, USA) for the MEF2-luciferase plasmid; Prof. Verfaillie (KU Leuven, Belgium) for Rag2-null;γc-null mice; Prof. Lewis (Cancer Research, UK) for Dll1flx/+ frozen 2-cell stage embryos; Professor Mazzone (VIB, KU Leuven, Belgium) for Rosa26::iCreERT2+/-mice; Prof. Fukada (University of Osaka, Japan) for SM/C-2.6 antibody. We thank Drs. Grosemans, Vochten and Raets for technical and administrative assistance. We thank also Paolo Luban and Rondoufonds voor Duchenne Onderzoek for kind donations. This work has been funded by 'Opening The Future' Campaign (EJJ-OPTFUT-02010), CARE-MI FP7, AFM, CARIPLO, FWO, GOA, IUAP and OT grants. MQ is supported by FWO Postdoctoral Fellowship, DC by IUAP Postdoctoral Grant. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2014 Macmillan Publishers Limited. All rights reserved.
PY - 2014/1/1
Y1 - 2014/1/1
N2 - 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.
AB - 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.
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U2 - 10.1038/cddis.2014.401
DO - 10.1038/cddis.2014.401
M3 - Article
C2 - 25299773
AN - SCOPUS:84928017925
SN - 2041-4889
VL - 5
JO - Cell Death and Disease
JF - Cell Death and Disease
IS - 10
M1 - e1448
ER -