| Literature DB >> 27184850 |
Gin-Wen Chang1, Cheng-Chih Hsiao2, Yen-Ming Peng1, Felipe A Vieira Braga3, Natasja A M Kragten3, Ester B M Remmerswaal4, Martijn D B van de Garde2, Rachel Straussberg5, Gabriele M König6, Evi Kostenis6, Vera Knäuper7, Linde Meyaard8, René A W van Lier3, Klaas P J M van Gisbergen3, Hsi-Hsien Lin9, Jörg Hamann10.
Abstract
Natural killer (NK) cells possess potent cytotoxic mechanisms that need to be tightly controlled. Here, we explored the regulation and function of GPR56/ADGRG1, an adhesion G protein-coupled receptor implicated in developmental processes and expressed distinctively in mature NK cells. Expression of GPR56 was triggered by Hobit (a homolog of Blimp-1 in T cells) and declined upon cell activation. Through studying NK cells from polymicrogyria patients with disease-causing mutations in ADGRG1, encoding GPR56, and NK-92 cells ectopically expressing the receptor, we found that GPR56 negatively regulates immediate effector functions, including production of inflammatory cytokines and cytolytic proteins, degranulation, and target cell killing. GPR56 pursues this activity by associating with the tetraspanin CD81. We conclude that GPR56 inhibits natural cytotoxicity of human NK cells.Entities:
Keywords: NK cells; adhesion GPCRs; cytotoxicity; immune regulation; transcription factor
Mesh:
Substances:
Year: 2016 PMID: 27184850 DOI: 10.1016/j.celrep.2016.04.053
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423