8 research outputs found

    Additional file 1: of HGF potentiates extracellular matrix-driven migration of human myoblasts: involvement of matrix metalloproteinases and MAPK/ERK pathway

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    A) depicts the mean fluorescence intensities (MFI) derived from cytofluorometry for detection of CD49d, CD49e, and CD49f integrin alpha-chains from myoblast cell lines. B) shows cytofluorometric histograms for CD56 immunodetection in CL25 and LHCN-M2 human myoblast clones. (TIFF 245 kb

    Additional file 2: of HGF potentiates extracellular matrix-driven migration of human myoblasts: involvement of matrix metalloproteinases and MAPK/ERK pathway

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    Kinetic analysis showing the spread area and cellular circularity of human myoblasts (CHQ cells) adhered onto ECM protiens, with or without HGF. **p < 0.01 versus BSA; ***p < 0.001. GT gelatin; LN laminin-111; FN fibronectin. (TIFF 181 kb

    Additional file 5: of HGF potentiates extracellular matrix-driven migration of human myoblasts: involvement of matrix metalloproteinases and MAPK/ERK pathway

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    Migration of human myoblast cell lines towards laminin-111 (LN) or Fibronectin (FN), in the presence or absence of HGF, with ou without it inhibitor (UO126). Graph bars represent means error standard, showing migration of LHCN-M2 (105 cells) and CL25 (5 × 104 cells) human myoblasts onto extracellular matrix protiens in the presence or not of 10 ng/ml HGF. Note that UO126 alone does not have any effect on cell migration, but it does block the enhancing effects of HGF upon LN- or FN-induced migration. ***p < 0.001. (TIFF 79 kb
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