Core engagement with ß-arrestin is dispensable for agonist-induced vasopressin receptor endocytosis and ERK activation.
Mol Biol Cell
; 28(8): 1003-1010, 2017 Apr 15.
Article
em En
| MEDLINE
| ID: mdl-28228552
ABSTRACT
G protein-coupled receptors (GPCRs) exhibit highly conserved activation and signaling mechanisms by which agonist stimulation leads to coupling of heterotrimeric G proteins and generation of second messenger response. This is followed by receptor phosphorylation, primarily in the carboxyl terminus but also in the cytoplasmic loops, and subsequent binding of arrestins. GPCRs typically recruit arrestins through two different sets of interactions, one involving phosphorylated receptor tail and the other mediated by the receptor core. The engagement of both set of interactions (tail and core) is generally believed to be necessary for arrestin-dependent functional outcomes such as receptor desensitization, endocytosis, and G protein-independent signaling. Here we demonstrate that a vasopressin receptor (V2R) mutant with truncated third intracellular loop (V2RΔICL3) can interact with ß-arrestin 1 (ßarr1) only through the phosphorylated tail without engaging the core interaction. Of interest, such a partially engaged V2RΔICL3-ßarr1 complex can efficiently interact with clathrin terminal domain and ERK2 MAPK in vitro. Furthermore, this core interaction-deficient V2R mutant exhibits efficient endocytosis and ERK activation upon agonist stimulation. Our data suggest that core interaction with ßarr is dispensable for V2R endocytosis and ERK activation and therefore provide novel insights into refining the current understanding of functional requirements in biphasic GPCR-ßarr interaction.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Receptores de Vasopressinas
/
Proteína Quinase 1 Ativada por Mitógeno
/
Beta-Arrestina 1
Idioma:
En
Ano de publicação:
2017
Tipo de documento:
Article