Figure 4
Figure 4. Western blot analysis of activated ERK1/2, STAT3, and AKT-1, and immunoprecipitation and Western blot analysis of activated c-MET in NK4-treated MM cells. (A) HGF-producing KMS11 and KMS34 cells as well as non–HGF-producing KMS27 cells were treated with 200 nM NK4 protein in RPMI containing 4% dialyzed FCS overnight; the cells were then incubated with or without 50 ng/mL HGF at room temperature for 20 minutes. The cell lysates were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), followed by immunoblotting with anti–phospho-ERK1/2, anti–phospho-STAT3, and anti–phospho-Ser473 AKT-1 antibodies. Blots were stripped and reprobed with anti-ERK1/2, anti-STAT3, and anti–AKT-1 antibodies. For evaluation of c-MET activation, MM cell lines were also treated with 200 nM NK4 in RPMI containing 4% dialyzed FCS overnight, and then incubated with or without 50 ng/mL HGF at room temperature for 5 minutes. After immunoprecipitation with anti–c-MET antibody, the immunocomplexes were subjected to SDS-PAGE. Immunoblotting was conducted with anti–phospho–c-MET antibody, and then the same filters were stripped and reprobed with anti–c-MET. (B) Densitometric analysis of the activation of c-MET and signal transducers. (C) Evaluation of c-MET activation in primary MM cells obtained from patient 1. Treatment of the MM cells and immunoprecipitation followed by Western blot analysis were performed as described.

Western blot analysis of activated ERK1/2, STAT3, and AKT-1, and immunoprecipitation and Western blot analysis of activated c-MET in NK4-treated MM cells. (A) HGF-producing KMS11 and KMS34 cells as well as non–HGF-producing KMS27 cells were treated with 200 nM NK4 protein in RPMI containing 4% dialyzed FCS overnight; the cells were then incubated with or without 50 ng/mL HGF at room temperature for 20 minutes. The cell lysates were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), followed by immunoblotting with anti–phospho-ERK1/2, anti–phospho-STAT3, and anti–phospho-Ser473 AKT-1 antibodies. Blots were stripped and reprobed with anti-ERK1/2, anti-STAT3, and anti–AKT-1 antibodies. For evaluation of c-MET activation, MM cell lines were also treated with 200 nM NK4 in RPMI containing 4% dialyzed FCS overnight, and then incubated with or without 50 ng/mL HGF at room temperature for 5 minutes. After immunoprecipitation with anti–c-MET antibody, the immunocomplexes were subjected to SDS-PAGE. Immunoblotting was conducted with anti–phospho–c-MET antibody, and then the same filters were stripped and reprobed with anti–c-MET. (B) Densitometric analysis of the activation of c-MET and signal transducers. (C) Evaluation of c-MET activation in primary MM cells obtained from patient 1. Treatment of the MM cells and immunoprecipitation followed by Western blot analysis were performed as described.

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