1. Academic Validation
  2. Kynurenic acid as a ligand for orphan G protein-coupled receptor GPR35

Kynurenic acid as a ligand for orphan G protein-coupled receptor GPR35

  • J Biol Chem. 2006 Aug 4;281(31):22021-22028. doi: 10.1074/jbc.M603503200.
Jinghong Wang 1 Nicole Simonavicius 1 Xiaosu Wu 1 Gayathri Swaminath 1 Jeff Reagan 1 Hui Tian 1 Lei Ling 2
Affiliations

Affiliations

  • 1 Amgen Inc., South San Francisco, California 94080.
  • 2 Amgen Inc., South San Francisco, California 94080. Electronic address: lling@amgen.com.
Abstract

Local catabolism of the essential amino acid tryptophan is considered an important mechanism in regulating immunological and neurological responses. The kynurenine pathway is the main route for the non-protein metabolism of tryptophan. The intermediates of the kynurenine pathway are present at micromolar concentrations in blood and are regulated by inflammatory stimuli. Here we show that GPR35, a previously orphan G protein-coupled receptor, functions as a receptor for the kynurenine pathway intermediate kynurenic acid. Kynurenic acid elicits calcium mobilization and inositol phosphate production in a GPR35-dependent manner in the presence of G(qi/o) chimeric G proteins. Kynurenic acid stimulates [35S]guanosine 5'-O-(3-thiotriphosphate) binding in GPR35-expressing cells, an effect abolished by pertussis toxin treatment. Kynurenic acid also induces the internalization of GPR35. Expression analysis indicates that GPR35 is predominantly detected in immune cells and the gastrointestinal tract. Furthermore, we show that kynurenic acid inhibits lipopolysaccharide-induced tumor necrosis factor-alpha secretion in peripheral blood mononuclear cells. Our results suggest unexpected signaling functions for kynurenic acid through GPR35 activation.

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