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β‐arrestins – scaffolds and signalling elements essential for WNT/Frizzled signalling pathways?
Author(s) -
Schulte Gunnar,
Schambony Alexandra,
Bryja Vítězslav
Publication year - 2010
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.2009.00466.x
Subject(s) - frizzled , microbiology and biotechnology , biology , wnt signaling pathway , dishevelled , g protein coupled receptor , arrestin , signal transduction , signalling , mediator , lrp6 , lrp5
beta-arrestins were originally identified as negative regulators of G protein-coupled receptor signalling. Recent studies have revealed that beta-arrestins serve as intracellular scaffolds and signalling intermediates. Their diverse functions in intracellular signalling pathways provide mechanisms for achieving signal specificity that might be attacked for pharmacological intervention. Here, we summarize the importance of beta-arrestin function for WNT [wingless (from Drosophila) and the oncogene int-1]/Frizzled (FZD) signalling. WNTs are secreted lipoglycoproteins that act through the seven transmembrane-spanning receptors of the FZD family. It recently became evident that beta-arrestins are required for cellular communication by means of WNTs and FZDs both in cellular systems and in vivo. Although the overall importance of arrestin for WNT/FZD signalling remains obscure, interaction with the central phosphoprotein Dishevelled and the endocytic machinery implicates beta-arrestin as a determinant of WNT signalling specificity, a mediator of WNT/FZD desensitization and a regulator of signalling compartmentation.