1. Academic Validation
  2. Internalization of CCR4 and inhibition of chemotaxis by K777, a potent and selective CCR4 antagonist

Internalization of CCR4 and inhibition of chemotaxis by K777, a potent and selective CCR4 antagonist

  • Pharmacology. 2013;91(5-6):305-13. doi: 10.1159/000350390.
Takashi Sato 1 Miho Iwase Motoki Miyama Masato Komai Etsuo Ohshima Akira Asai Hiroshi Yano Ichiro Miki
Affiliations

Affiliation

  • 1 Drug Discovery Research Laboratories, Fuji Research Park, Kyowa Hakko Kirin Co., Ltd., Nagaizumi, Japan.
Abstract

CC Chemokine Receptor 4 (CCR4) is a G protein-coupled receptor that regulates the chemotaxis of Th2 lymphocytes, which are key players in allergic diseases. K777 is a small compound identified in a binding assay using a CCR4 ligand, CCL17. K777 inhibited both CCL17 binding and CCL17-induced chemotaxis in Hut78 cells (IC50: 57 and 8.9 nmol/l, respectively). The K777-mediated inhibition of chemotaxis was potent even in the presence of a 10-fold higher concentration of CCL17. The imaging and flow cytometric analyses revealed that K777 induced CCR4 internalization, with a ∼50% reduction of cell surface CCR4. K777 did not inhibit CXCR4-induced chemotaxis or internalization and did not bring about CA(2+) mobilization by itself. A Scatchard plot analysis of the binding assay using radiolabeled K777 revealed a single high-affinity binding site on the CCR4 molecule. These results indicate that K777 is a selective CCR4 Antagonist featuring the potent chemotaxis inhibition, to which the internalization-inducible ability of K777 to hide a part of cell surface CCR4 may contribute.

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