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Human cardiac stem cells exhibit mesenchymal features and are maintained through Akt/GSK-3beta signaling.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2007 Jan 19; Vol. 352 (3), pp. 635-41. Date of Electronic Publication: 2006 Nov 27. - Publication Year :
- 2007
-
Abstract
- Recent evidence suggested that human cardiac stem cells (hCSCs) may have the clinical application for cardiac repair; however, their characteristics and the regulatory mechanisms of their growth have not been fully investigated. Here, we show the novel property of hCSCs with respect to their origin and tissue distribution in human heart, and demonstrate the signaling pathway that regulates their growth and survival. Telomerase-active hCSCs were predominantly present in the right atrium and outflow tract of the heart (infant > adult) and had a mesenchymal cell-like phenotype. These hCSCs expressed the embryonic stem cell markers and differentiated into cardiomyocytes to support cardiac function when transplanted them into ischemic myocardium. Inhibition of Akt pathway impaired the hCSC proliferation and induced apoptosis, whereas inhibition of glycogen synthase kinase-3 (GSK-3) enhanced their growth and survival. We conclude that hCSCs exhibit mesenchymal features and that Akt/GSK-3beta may be crucial modulators for hCSC maintenance in human heart.
- Subjects :
- Adult
Aged
Cell Differentiation
Cell Proliferation
Cell Survival
Cells, Cultured
Child
Child, Preschool
Female
Glycogen Synthase Kinase 3 beta
Humans
Infant
Infant, Newborn
Male
Middle Aged
Glycogen Synthase Kinase 3 metabolism
Mesenchymal Stem Cells cytology
Mesenchymal Stem Cells metabolism
Myocytes, Cardiac cytology
Myocytes, Cardiac metabolism
Oncogene Protein v-akt metabolism
Signal Transduction physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 352
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 17150190
- Full Text :
- https://doi.org/10.1016/j.bbrc.2006.11.096