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ESCRT Proteins and Cell Signalling
Author(s) -
Wegner Catherine Sem,
Rodahl Lina M. W.,
Stenmark Harald
Publication year - 2011
Publication title -
traffic
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.677
H-Index - 130
eISSN - 1600-0854
pISSN - 1398-9219
DOI - 10.1111/j.1600-0854.2011.01210.x
Subject(s) - escrt , endosome , microbiology and biotechnology , biology , ubiquitin , endocytic cycle , protein targeting , tsg101 , receptor , membrane protein , endocytosis , biochemistry , intracellular , microvesicles , membrane , microrna , gene
Subunits of the endosomal sorting complex required for transport (ESCRT) were identified as components of a molecular machinery that sorts ubiquitinated membrane proteins into the intraluminal vesicles (ILVs) of multivesicular endosomes (MVEs) for subsequent delivery to the lumen of lysosomes or related organelles. As many of the membrane proteins that undergo ESCRT‐mediated sorting are signalling receptors that are ubiquitinated in response to ligand binding, ESCRT subunits have been hypothesized to play a crucial role in attenuation of cell signalling by mediating ligand‐induced receptor degradation. Here we discuss this concept based on the examples from loss‐of‐function studies in model organisms and cell lines. The emerging picture is that ESCRTs are indeed involved in downregulation of receptor signalling pathways associated with cell survival, proliferation and polarity. In addition, the recent discovery of a positive role for the ESCRT pathway in Wnt signalling through sequestration of an inhibitory cytosolic component into MVEs illustrates that ESCRTs may also control signalling in ways that are independent of degradative receptor sorting.