Abstract
The effects of muscle splice variants of insulin-like growth factor I (IGF-I) on proliferation and differentiation were studied in human primary muscle cell cultures from healthy subjects as well as from muscular dystrophy and ALS patients. Although the initial numbers of mononucleated progenitor cells expressing desmin were lower in diseased muscle, the E domain peptide of IGF-IEc (MGF) significantly increased the numbers of progenitor cells in healthy and diseased muscle. IGF-I significantly enhances myogenic differentiation whereas MGF E peptide blocks this pathway, resulting in an increased progenitor (stem) cell pool and thus potentially facilitating repair and maintenance of this postmitotic tissue.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Alternative Splicing*
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Antibodies, Monoclonal / pharmacology
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Cell Proliferation / drug effects
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Cells, Cultured
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Creatine Kinase / metabolism
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Desmin / analysis
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Dose-Response Relationship, Drug
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Humans
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Immunohistochemistry
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Insulin-Like Growth Factor I / genetics
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Insulin-Like Growth Factor I / pharmacology*
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Microscopy, Fluorescence
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Muscle, Skeletal / cytology
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Muscle, Skeletal / drug effects*
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Muscle, Skeletal / metabolism
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Muscular Atrophy / congenital
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Muscular Atrophy / metabolism
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Muscular Atrophy / pathology
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Protein Isoforms / pharmacology
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Receptor, IGF Type 1 / immunology
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Receptor, IGF Type 1 / metabolism
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Stem Cells / cytology
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Stem Cells / drug effects*
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Stem Cells / metabolism
Substances
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Antibodies, Monoclonal
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Desmin
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Protein Isoforms
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Insulin-Like Growth Factor I
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Receptor, IGF Type 1
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Creatine Kinase