Ligand-dependent Toll-like receptor 4 (TLR4)-oligomerization is directly linked with TLR4-signaling

Author:

Saitoh Shin-ichiroh1,Akashi Sachiko1,Yamada Takenao2,Tanimura Natsuko2,Matsumoto Fumi2,Fukase Koichi3,Kusumoto Shoichi3,Kosugi Atsushi4,Miyake Kensuke5

Affiliation:

1. Division of Infectious Genetics, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan

2. Department of Medical Technology and Science, Osaka University, Osaka, Japan

3. Department of Chemistry, Graduate School of Science, Osaka University, Osaka, Japan

4. Department of Medical Technology and Science, Osaka University, Osaka, Japan, CREST, Japan Science and Technology Corporation, Tokyo, Japan

5. Division of Infectious Genetics, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan, -tokyo.ac.jp, CREST, Japan Science and Technology Corporation, Tokyo, Japan

Abstract

Toll-like receptor 4 (TLR4) and MD-2 recognize lipid A, the active moiety of microbial lipopolysaccharide (LPS). Little is known about mechanisms for LPS recognition by TLR4/MD-2. We here showed, by using in vitro transfectants, ligand-induced TLR4-oligomerization, which required both membrane CD14 and MD-2. We previously reported that lipid IVa, a lipid A precursor, is agonistic on mouse TLR4/MD-2 but antagonistic on human TLR4/MD-2 and chimeric mouse TLR4/human MD-2. Lipid IVa triggered oligomerization of mouse TLR4/MD-2 but not human TLR4/MD-2 or chimeric mouse TLR4/human MD-2. Further, lipid IVa inhibited lipid A-dependent oligomerization of chimeric mouse TLR4/human MD-2. These results demonstrate that ligand-induced TLR4-oligomerization is directly linked with TLR4-signaling and suggest that MD-2 has an important role in regulating TLR4-oligomerization.

Publisher

SAGE Publications

Subject

Infectious Diseases,Cell Biology,Molecular Biology,Immunology,Microbiology

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