Ezrin-Dependent Promotion of Glioma Cell Clonogenicity, Motility, and Invasion Mediated by BCL-2 and Transforming Growth Factor-β2

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Fig. 5.
Fig. 5.

HGF-promoted glioma cell migration requires enhanced TGF-β2. A, LN-229 neo or nter-ezrin cells were untreated or exposed to HGF (10 ng/ml) for 24 hr and analyzed for TGF-β2 release as in Figure4A. B, LN-229 and U87MG cells were treated with HGF (10 ng/ml for 24 hr) or TGF-β2 antibody as in Figure 4B, as indicated, and assessed for migration (mean and SEM; n = 3; ttest; *p < 0.05 for the effect of HGF;#p < 0.05 for the effect of TGF-β2 antibody compared with control antibody-treated cells; +p < 0.05 for the effect of TGF-β2 antibody plus HGF compared with HGF alone).C, The cells were untreated or treated with TGF-β2 (2 ng/ml) or HGF (10 ng/ml) and assessed for colony formation as in Figure 1C (mean and SEM;n = 3; t test; *p < 0.05; **p < 0.01 for the effect of dominant-negative ezrin; ++p< 0.01 for the effect of TGF-β2 compared with nontreated isogenic cells).

  1. The Journal of Neuroscience vol. 21 no. 10 3360-3368
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