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pubmed-article:10471395pubmed:abstractTextTo examine the effectiveness of a gene transfer of bone morphogenetic protein (BMP)-2 into C2C12 myoblasts, we constructed a human BMP-2-expressing replication-deficient adenoviral vector, AxCAOBMP-2. C2C12 cells were infected in vitro with either this viral vector or an Escherichia coli LacZ gene-expressing control adenovirus vector. An efficient gene transfer to the C2C12 cells was confirmed with the LacZ gene-expressing vector by X-gal staining. Abundant BMP-2 expression in C2C12 cells infected with this viral vector was confirmed by immunofluorescence and Western blot analysis. C2C12 cells transferred with the BMP-2 gene by this vector produced alkaline phosphatase in the cells and also produced and secreted osteocalcin in the culture medium, demonstrating that a gene transfer of BMP-2 into C2C12 cells in vitro could convert these cells from myoblast to osteoblast lineage.lld:pubmed
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pubmed-article:10471395pubmed:copyrightInfoCopyright 1999 Academic Press.lld:pubmed
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pubmed-article:10471395pubmed:pagination739-43lld:pubmed
pubmed-article:10471395pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:10471395pubmed:articleTitleExpression of bone morphogenetic protein-2 via adenoviral vector in C2C12 myoblasts induces differentiation into the osteoblast lineage.lld:pubmed
pubmed-article:10471395pubmed:affiliationGraduate School of Medicine, Kyoto University, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.lld:pubmed
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