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Erschienen in: Basic Research in Cardiology 6/2008

01.11.2008 | ORIGINAL CONTRIBUTION

TGF-β1 enhances cardiomyogenic differentiation of skeletal muscle-derived adult primitive cells

verfasst von: Ahmed Abdel-Latif, MD, Ewa K. Zuba-Surma, PhD, Jamie Case, PhD, Sumit Tiwari, MD, Greg Hunt, BS, Smita Ranjan, BS, Robert J. Vincent, BS, Edward F. Srour, PhD, Roberto Bolli, MD, Buddhadeb Dawn, MD

Erschienen in: Basic Research in Cardiology | Ausgabe 6/2008

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Abstract

The optimal medium for cardiac differentiation of adult primitive cells remains to be established. We quantitatively compared the efficacy of IGF-1, dynorphin B, insulin, oxytocin, bFGF, and TGF-β1 in inducing cardiomyogenic differentiation. Adult mouse skeletal muscle-derived Sca1+/CD45-/c-kit-/Thy-1+ (SM+) and Sca1-/CD45-/c-kit-/Thy-1+ (SM-) cells were cultured in basic medium (BM; DMEM, FBS, IGF-1, dynorphin B) alone and BM supplemented with insulin, oxytocin, bFGF, or TGF-β1. Cardiac differentiation was evaluated by the expression of cardiac-specific markers at the mRNA (qRT-PCR) and protein (immunocytochemistry) levels. BM+TGF-β1 upregulated mRNA expression of Nkx2.5 and GATA-4 after 4 days and Myl2 after 9 days. After 30 days, BM+TGF-β1 induced the greatest extent of cardiac differentiation (by morphology and expression of cardiac markers) in SM- cells. We conclude that TGF-β1 enhances cardiomyogenic differentiation in skeletal muscle-derived adult primitive cells. This strategy may be utilized to induce cardiac differentiation as well as to examine the cardiomyogenic potential of adult tissue-derived stem/progenitor cells.
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Metadaten
Titel
TGF-β1 enhances cardiomyogenic differentiation of skeletal muscle-derived adult primitive cells
verfasst von
Ahmed Abdel-Latif, MD
Ewa K. Zuba-Surma, PhD
Jamie Case, PhD
Sumit Tiwari, MD
Greg Hunt, BS
Smita Ranjan, BS
Robert J. Vincent, BS
Edward F. Srour, PhD
Roberto Bolli, MD
Buddhadeb Dawn, MD
Publikationsdatum
01.11.2008
Verlag
D. Steinkopff-Verlag
Erschienen in
Basic Research in Cardiology / Ausgabe 6/2008
Print ISSN: 0300-8428
Elektronische ISSN: 1435-1803
DOI
https://doi.org/10.1007/s00395-008-0729-9

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