Chemerin-activated functions of CMKLR1 are regulated by G protein-coupled receptor kinase 6 (GRK6) and β-arrestin 2 in inflammatory macrophages.

Journal Article (Journal Article)

Chemerin receptor (CMKLR1) is a G protein-coupled receptor (GPCR) implicated in macrophage-mediated inflammation and in several forms of human arthritis. Analogous to other GPCR, CMKLR1 is likely regulated by G protein-coupled receptor kinase (GRK) phosphorylation of intracellular domains in an activation-dependent manner, which leads to recruitment and termination of intracellular signaling via desensitization and internalization of the receptor. The ubiquitously expressed GRK family members include GRK2, GRK3, GRK5, and GRK6, but it is unknown which GRK regulates CMKLR1 cellular and signaling functions. Our data show that activation of CMKLR1 by chemerin in primary macrophages leads to signaling and functional outcomes that are regulated by GRK6 and β-arrestin 2. We show that arrestin recruitment to CMKLR1 following chemerin stimulation is enhanced with co-expression of GRK6. Further, internalization of endogenous CMKLR1, following the addition of chemerin, is decreased in inflammatory macrophages from GRK6- and β-arrestin 2-deficient mice. These GRK6- and β-arrestin 2-deficient macrophages display increased migration toward chemerin and altered AKT and Extracellular-signal Related Kinase (ERK) signaling. Our findings show that chemerin-activated CMKLR1 regulation in inflammatory macrophages is largely GRK6 and β-arrestin mediated, which may impact innate immunity and have therapeutic implications in rheumatic disease.

Full Text

Duke Authors

Cited Authors

  • Serafin, DS; Allyn, B; Sassano, MF; Timoshchenko, RG; Mattox, D; Brozowski, JM; Siderovski, DP; Truong, YK; Esserman, D; Tarrant, TK; Billard, MJ

Published Date

  • February 2019

Published In

Volume / Issue

  • 106 /

Start / End Page

  • 12 - 21

PubMed ID

  • 30576947

Pubmed Central ID

  • PMC6584946

Electronic International Standard Serial Number (EISSN)

  • 1872-9142

Digital Object Identifier (DOI)

  • 10.1016/j.molimm.2018.12.016


  • eng

Conference Location

  • England