Mutation of putative phosphorylation sites in the free fatty acid receptor 1: Effects on signaling, receptor phosphorylation, and internalization

Mol Cell Endocrinol. 2022 Apr 5:545:111573. doi: 10.1016/j.mce.2022.111573. Epub 2022 Jan 20.

Abstract

Free fatty acid receptor 1 phosphorylation sites were studied using mutants, including a) a mutant with T215V in the third intracellular loop (3IL), b) another with changes in the carboxyl terminus (C-term): T287V, T293V, S298A, and c) a mutant with all of these changes (3IL/C-term). Agonist-induced increases in intracellular calcium were similar between cells expressing wild-type or mutant receptors. In contrast, agonist-induced FFA1 receptor phosphorylation was reduced in mutants compared to wild type. Phorbol ester-induced FFA1 receptor phosphorylation was rapid and robust in cells expressing the wild-type receptor and essentially abolished in the mutants. Agonist-induced ERK 1/2 phosphorylation and receptor internalization were decreased in cells expressing the mutant receptors compared to those expressing the wild-type receptor. Our data suggest that the identified sites might participate in receptor phosphorylation, signaling, and internalization.

Keywords: FFA1 receptor; Free fatty acid receptor 1; GPR40; Receptor phosphorylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fatty Acids, Nonesterified*
  • Humans
  • Mutation / genetics
  • Phosphorylation
  • Receptors, G-Protein-Coupled / metabolism*
  • Signal Transduction

Substances

  • FFAR1 protein, human
  • Fatty Acids, Nonesterified
  • Receptors, G-Protein-Coupled