Sequestration of G?? by deubiquitinated arrestins into the nucleus as a novel desensitization mechanism of G protein-coupled receptors.

Desensitization of G protein-coupled receptors (GPCRs) refers to a rapid attenuation of responsiveness that occurs with repeated or continuous exposure to agonists. GRK-mediated phosphorylation and subsequent binding with arrestins in the activated receptor cytoplasmic cavity in competition with G proteins has been suggested as the conventional mechanism of desensitization. Along ...
with widely accepted conventional mechanism of desensitization, studies of various GPCRs including dopamine D2-like receptors (D2R, D3R, D4R) have suggested the existence of another desensitization mechanism. In this study, loss-of-function approaches and D2-like receptor mutants that display different desensitization properties were used to elucidate the molecular mechanisms responsible for desensitization.Desensitization development entailed the signaling cascade composed of Src, PDK1, and Akt, the latter of which in turn interacted with USP33, an arrestin deubiquitinase, to promote arrestin deubiquitination. The deubiquitinated arrestin subsequently formed a complex with G?? and translocated to the nucleus via an importin complex, wherein it sequestered G?? from the receptor and G?, thereby attenuating receptor signaling. As in D2-like receptors, both USP33 and importin ?1 were involved in the desensitization of the ?2 adrenoceptor.In addition to the conventional mechanism of desensitization, which occurs on the plasma membrane and in the cytosol, this study provides a new insight that another desensitization pathway in which nuclear trafficking plays a critical role is operating. It is plausible that multiple, complementary desensitization measures are in place to properly induce desensitization depending on receptor characteristics or the surrounding environment. Video Abstract.
Mesh Terms:
Arrestin, Arrestins, Phosphorylation, Receptors, G-Protein-Coupled, Signal Transduction, beta-Arrestins
Cell Commun Signal
Date: Jan. 19, 2023
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