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The Journal of Neuroscience, May 15, 2001, 21(10):3360-3368

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

Wolfgang Wick1, Cornelia Grimmel1, Christine Wild-Bode1, Michael Platten1, Monique Arpin2, and Michael Weller1

1 Laboratory of Molecular Neuro-Oncology, Department of Neurology, University of Tübingen, School of Medicine, Tübingen, Germany, and 2 Laboratoire de Morphogenese et Signalisation Cellulaires, Unité Mixte de Recherche, 144 Centre National de la Recherche Scientifique/Institut Curie, 75248 Paris Cedex 05, France

Ezrin belongs to the ezrin-radixin-moesin family proteins, which cross-link actin cytoskeleton and plasma membrane. Malignant glioma cells are paradigmatic for their strong migratory and invasive properties. Here, we report that the expression of dominant-negative ezrins inhibits clonogenicity, migration, and invasiveness of human malignant glioma cells. Furthermore, dominant-negative ezrins block hepatocyte growth factor (HGF)-mediated stimulation of clonogenicity and migration, without altering HGF-induced protein kinase B/Akt and focal adhesion kinase phosphorylation. Glioma cells expressing dominant-negative ezrins exhibit a shift of the BCL-2/BAX rheostat toward apoptosis, reduced alpha Vbeta 3 integrin expression and reduced matrix metalloproteinase (MMP) expression and activity. These changes are associated with a dramatic loss of transforming growth factor beta 2 (TGF-beta 2) release. Exogenous supplementation of TGF-beta 2 overcomes the inhibitory effects of dominant-negative ezrins on migration and clonogenicity. A neutralizing TGF-beta 2 antibody mimics the effects of dominant-negative ezrins on clonogenicity and migration. Exogenous HGF markedly induces TGF-beta 2 protein levels, and a neutralizing TGF-beta 2 antibody abolishes the HGF-mediated increase in glioma cell motility. Finally, TGF-beta 2 does not modulate BCL-2 or BAX expression, but BCL-2 gene transfer increases the levels of latent and active TGF-beta 2. Intracranial xenografts of U87MG glioma cells transfected with the dominant-negative ezrins in athymic mice grow to significantly smaller volumes, and the median survival of these mice is 50 d compared with 28 d in the control group. These data define a novel pathway for HGF-induced glioma cell migration and invasion, which requires ezrin, changes in the BCL-2/BAX rheostat, and the induction of TGF-beta 2 expression in vitro, and underscore the important role of HGF signaling in vivo.

Key words: brain tumor; ERM proteins; motility; TGF-beta ; BCL-2; metalloproteinases; HGF; athymic mice


Copyright © 2001 Society for Neuroscience  0270-6474/01/21103360-09$05.00/0


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