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Effective myotube formation in human adipose tissue-derived stem cells expressing dystrophin and myosin heavy chain by cellular fusion with mouse C2C12 myoblasts.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2011 Apr 29; Vol. 408 (1), pp. 167-73. Date of Electronic Publication: 2011 Apr 05. - Publication Year :
- 2011
-
Abstract
- Stem cell therapy for muscular dystrophies requires stem cells that are able to participate in the formation of new muscle fibers. However, the differentiation steps that are the most critical for this process are not clear. We investigated the myogenic phases of human adipose tissue-derived stem cells (hASCs) step by step and the capability of myotube formation according to the differentiation phase by cellular fusion with mouse myoblast C2C12 cells. In hASCs treated with 5-azacytidine and fibroblast growth factor-2 (FGF-2) for 1 day, the early differentiation step to express MyoD and myogenin was induced by FGF-2 treatment for 6 days. Dystrophin and myosin heavy chain (MyHC) expression was induced by hASC conditioned medium in the late differentiation step. Myotubes were observed only in hASCs undergoing the late differentiation step by cellular fusion with C2C12 cells. In contrast, hASCs that were normal or in the early stage were not involved in myotube formation. Our results indicate that stem cells expressing dystrophin and MyHC are more suitable for myotube formation by co-culture with myoblasts than normal or early differentiated stem cells expressing MyoD and myogenin.<br /> (Copyright © 2011 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Cell Fusion
Cell Line
Cell Lineage
Coculture Techniques
Humans
Mice
Muscle Fibers, Skeletal metabolism
Myoblasts metabolism
Regeneration
Stem Cells metabolism
Adipose Tissue cytology
Cell Differentiation
Dystrophin biosynthesis
Muscle Development
Muscle Fibers, Skeletal physiology
Myoblasts physiology
Myosin Heavy Chains biosynthesis
Stem Cells physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 408
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 21473854
- Full Text :
- https://doi.org/10.1016/j.bbrc.2011.04.002