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Clathrin-Independent Endocytosis Suppresses Cancer Cell Blebbing and Invasion
Author(s) -
Mikkel R. Holst,
Maite VidalQuadras,
Elin Larsson,
JieYoung Song,
Madlen Hubert,
Jeanette Blomberg,
Magnus Lundborg,
Maréne Landström,
Richard Lundmark
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.08.006
Subject(s) - endocytosis , microbiology and biotechnology , endocytic cycle , clathrin , cancer cell , internalization , biology , receptor mediated endocytosis , motility , cell membrane , cell , cancer , biochemistry , genetics
Cellular blebbing, caused by local alterations in cell-surface tension, has been shown to increase the invasiveness of cancer cells. However, the regulatory mechanisms balancing cell-surface dynamics and bleb formation remain elusive. Here, we show that an acute reduction in cell volume activates clathrin-independent endocytosis. Hence, a decrease in surface tension is buffered by the internalization of the plasma membrane (PM) lipid bilayer. Membrane invagination and endocytosis are driven by the tension-mediated recruitment of the membrane sculpting and GTPase-activating protein GRAF1 (GTPase regulator associated with focal adhesion kinase-1) to the PM. Disruption of this regulation by depleting cells of GRAF1 or mutating key phosphatidylinositol-interacting amino acids in the protein results in increased cellular blebbing and promotes the 3D motility of cancer cells. Our data support a role for clathrin-independent endocytic machinery in balancing membrane tension, which clarifies the previously reported role of GRAF1 as a tumor suppressor.

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