Direct recognition of the mycobacterial glycolipid, trehalose dimycolate, by C-type lectin Mincle

Author:

Ishikawa Eri1,Ishikawa Tetsuaki12,Morita Yasu S.33,Toyonaga Kenji1,Yamada Hisakata1,Takeuchi Osamu33,Kinoshita Taroh33,Akira Shizuo33,Yoshikai Yasunobu1,Yamasaki Sho1

Affiliation:

1. Division of Molecular Immunology, Division of Host Defense, Medical Institute of Bioregulation, Kyushu University, Fukuoka 812-8582, Japan

2. Cell Signaling, Chiba University School of Medicine, Chiba 260-8670, Japan

3. Department of Immunoregulation, Department of Host Defense, Research Institute for Microbial Diseases, Laboratory of Immunoglycobiology, Laboratory of Host Defense, WPI Immunology Frontier Research Center, Osaka University, Suita 565-0871, Japan

Abstract

Tuberculosis remains a fatal disease caused by Mycobacterium tuberculosis, which contains various unique components that affect the host immune system. Trehalose-6,6′-dimycolate (TDM; also called cord factor) is a mycobacterial cell wall glycolipid that is the most studied immunostimulatory component of M. tuberculosis. Despite five decades of research on TDM, its host receptor has not been clearly identified. Here, we demonstrate that macrophage inducible C-type lectin (Mincle) is an essential receptor for TDM. Heat-killed mycobacteria activated Mincle-expressing cells, but the activity was lost upon delipidation of the bacteria; analysis of the lipid extracts identified TDM as a Mincle ligand. TDM activated macrophages to produce inflammatory cytokines and nitric oxide, which are completely suppressed in Mincle-deficient macrophages. In vivo TDM administration induced a robust elevation of inflammatory cytokines in sera and characteristic lung inflammation, such as granuloma formation. However, no TDM-induced lung granuloma was formed in Mincle-deficient mice. Whole mycobacteria were able to activate macrophages even in MyD88-deficient background, but the activation was significantly diminished in Mincle/MyD88 double-deficient macrophages. These results demonstrate that Mincle is an essential receptor for the mycobacterial glycolipid, TDM.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

Reference42 articles.

1. The granulomatous inflammatory response. A review;Adams;Am. J. Pathol.,1976

2. Pathogen recognition and innate immunity;Akira;Cell.,2006

3. Two subsites on the active center of pig kidney trehalase;Asano;Eur. J. Biochem.,1996

4. Development of immunoadjuvants for immunotherapy of cancer;Azuma;Int. Immunopharmacol.,2001

5. Modes of action of Freund's adjuvants in experimental models of autoimmune diseases;Billiau;J. Leukoc. Biol.,2001

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