Literature DB >> 21518165

ESCRT proteins and cell signalling.

Catherine Sem Wegner1, Lina M W Rodahl, Harald Stenmark.   

Abstract

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.
© 2011 John Wiley & Sons A/S.

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Year:  2011        PMID: 21518165     DOI: 10.1111/j.1600-0854.2011.01210.x

Source DB:  PubMed          Journal:  Traffic        ISSN: 1398-9219            Impact factor:   6.215


  26 in total

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5.  Cofactors required for TLR7- and TLR9-dependent innate immune responses.

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Journal:  Cell Host Microbe       Date:  2012-03-15       Impact factor: 21.023

6.  Mechanisms of negative membrane curvature sensing and generation by ESCRT III subunit Snf7.

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Review 7.  Structure and function of the membrane deformation AAA ATPase Vps4.

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Review 10.  The balance of protein expression and degradation: an ESCRTs point of view.

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