2009
DOI: 10.1055/s-0029-1191349
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Polyurethane scaffolds seeded with genetically engineered skeletal myoblasts: a promising tool to regenerate myocardial function

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Cited by 4 publications
(14 citation statements)
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“…The plasmid was a generous gift from Kensuke Egashira (Kyushu University, Fukuoka, Japan). Effective transfection of the cells and overexpression of SDF-1 were confirmed in vitro by RT-PCR and ELISA as reported in our previous study [18]. Injected SkM-SDF-1 secreted around 18% more SDF than untransfected myoblasts.…”
Section: Transfection Of Primary Skeletal Myoblastssupporting
confidence: 82%
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“…The plasmid was a generous gift from Kensuke Egashira (Kyushu University, Fukuoka, Japan). Effective transfection of the cells and overexpression of SDF-1 were confirmed in vitro by RT-PCR and ELISA as reported in our previous study [18]. Injected SkM-SDF-1 secreted around 18% more SDF than untransfected myoblasts.…”
Section: Transfection Of Primary Skeletal Myoblastssupporting
confidence: 82%
“…Previous studies suggested a scaffold-based application of transplanted cells to improve study outcome by avoiding cell loss due to injection, diffusion, or poor engraftment and by preventing injection-induced arrhythmias [18,24]. Unexpectedly, the scaffold-based application of SDF-1 expressing myoblasts to the infarcted heart did not further enhance the positive effects on systolic function observed in group Inj-SDF-1-SkM.…”
Section: Assessment Of Hemodynamic Parametersmentioning
confidence: 84%
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“…8 In brief, the plasmid pcDNA3-huda-Akt (expressing a myristinylated dominant-active form of Akt1) was delivered into SkM using the liposome-based transfection reagent Metafectene Pro (Biontex, Munich, Germany). According to the manufacturer's protocol, we incubated 5 g plasmid DNA (diluted in 100 l MEM) with 12 L Metafectene Pro solution (diluted in 100 l MEM) for 25 min at room temperature.…”
Section: Transfection Of Primary Skeletal Myoblastsmentioning
confidence: 99%