Control of the adaptive response of the heart to stress via the Notch1 receptor pathway.

Détails

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Etat: Public
Version: de l'auteur
ID Serval
serval:BIB_123D76E4A2C7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Control of the adaptive response of the heart to stress via the Notch1 receptor pathway.
Périodique
Journal of Experimental Medicine
Auteur(s)
Croquelois A., Domenighetti A.A., Nemir M., Lepore M., Rosenblatt-Velin N., Radtke F., Pedrazzini T.
ISSN
0022-1007
Statut éditorial
Publié
Date de publication
2008
Peer-reviewed
Oui
Volume
205
Numéro
13
Pages
3173-3185
Langue
anglais
Résumé
In the damaged heart, cardiac adaptation relies primarily on cardiomyocyte hypertrophy. The recent discovery of cardiac stem cells in the postnatal heart, however, suggests that these cells could participate in the response to stress via their capacity to regenerate cardiac tissues. Using models of cardiac hypertrophy and failure, we demonstrate that components of the Notch pathway are up-regulated in the hypertrophic heart. The Notch pathway is an evolutionarily conserved cell-to-cell communication system, which is crucial in many developmental processes. Notch also plays key roles in the regenerative capacity of self-renewing organs. In the heart, Notch1 signaling takes place in cardiomyocytes and in mesenchymal cardiac precursors and is activated secondary to stimulated Jagged1 expression on the surface of cardiomyocytes. Using mice lacking Notch1 expression specifically in the heart, we show that the Notch1 pathway controls pathophysiological cardiac remodeling. In the absence of Notch1, cardiac hypertrophy is exacerbated, fibrosis develops, function is altered, and the mortality rate increases. Therefore, in cardiomyocytes, Notch controls maturation, limits the extent of the hypertrophic response, and may thereby contribute to cell survival. In cardiac precursors, Notch prevents cardiogenic differentiation, favors proliferation, and may facilitate the expansion of a transient amplifying cell compartment.
Mots-clé
Alanine/analogs & derivatives, Alanine/metabolism, Amyloid Precursor Protein Secretases/antagonists & inhibitors, Animals, Apoptosis/physiology, Azepines/metabolism, Cell Differentiation/physiology, Cells, Cultured, Gene Expression Regulation, Heart/physiology, Mice, Mice, Knockout, Mice, Transgenic, Myocardium/metabolism, Myocardium/pathology, Myocytes, Cardiac/cytology, Myocytes, Cardiac/physiology, Oligonucleotide Array Sequence Analysis, Receptor, Notch1/genetics, Receptor, Notch1/metabolism, Signal Transduction/physiology, Stem Cells/cytology, Stem Cells/metabolism, Stress, Physiological
Pubmed
Web of science
Open Access
Oui
Création de la notice
02/10/2009 17:32
Dernière modification de la notice
20/08/2019 13:40
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