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DENND2B activates Rab13 at the leading edge of migrating cells and promotes metastatic behavior
Authors:Maria S. Ioannou  Emily S. Bell  Martine Girard  Mathilde Chaineau  Jason N.R. Hamlin  Mark Daubaras  Anie Monast  Morag Park  Louis Hodgson  Peter S. McPherson
Affiliation:1.Department of Neurology and Neurosurgery, Montreal Neurological Institute; and 2.Department of Biochemistry, Goodman Cancer Centre; McGill University, Montreal, Quebec H3A 0G4, Canada;3.Department of Anatomy and Structural Biology, Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, New York, NY 10461
Abstract:The small guanosine triphosphatase Rab13 functions in exocytic vesicle trafficking in epithelial cells. Alterations in Rab13 activity have been observed in human cancers, yet the mechanism of Rab13 activation and its role in cancer progression remain unclear. In this paper, we identify the DENN domain protein DENND2B as the guanine nucleotide exchange factor for Rab13 and develop a novel Förster resonance energy transfer–based Rab biosensor to reveal activation of Rab13 by DENND2B at the leading edge of migrating cells. DENND2B interacts with the Rab13 effector MICAL-L2 at the cell periphery, and this interaction is required for the dynamic remodeling of the cell’s leading edge. Disruption of Rab13-mediated trafficking dramatically limits the invasive behavior of epithelial cells in vitro and the growth and migration of highly invasive cancer cells in vivo. Thus, blocking Rab13 activation by DENND2B may provide a novel target to limit the spread of epithelial cancers.
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