| Literature DB >> 28834752 |
Mikkel Roland Holst1, Maite Vidal-Quadras1, Elin Larsson2, Jie Song3, Madlen Hubert1, Jeanette Blomberg2, Magnus Lundborg4, Maréne Landström3, Richard Lundmark5.
Abstract
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.Entities:
Keywords: ARHGAP26; Endocytosis; GRAF1; GRAF1-dependent endocytosis; cancer invasion; cell migration; cell surface dynamics; clathrin-independent endocytosis; membrane blebbing; membrane tension
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Year: 2017 PMID: 28834752 DOI: 10.1016/j.celrep.2017.08.006
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423