Cutting Edge: Endotoxin Tolerance in Mouse Peritoneal Macrophages Correlates with Down-Regulation of Surface Toll-Like Receptor 4 Expression

Fumiko Nomura(Hyogo Medical University), Sachiko Akashi(Saga Medical School Hospital), Yoshimitsu Sakao(Japan Science and Technology Agency), Shintaro Sato(Japan Science and Technology Agency), Taro Kawai(Japan Science and Technology Agency), Makoto Matsumoto(Japan Science and Technology Agency), Kenji Nakanishi(Hyogo Medical University), Masao Kimoto(Saga Medical School Hospital), Kensuke Miyake(Saga Medical School Hospital), Kiyoshi Takeda(Japan Science and Technology Agency), Shizuo Akira(Japan Science and Technology Agency)
The Journal of Immunology
April 1, 2000
Cited by 771

Abstract

Monocytes/macrophages exposed to LPS show reduced responses to second stimulation with LPS, which is termed LPS tolerance. In this study, we investigated molecular mechanism of LPS tolerance in macrophages. Mouse peritoneal macrophages pre-exposed to LPS exhibited reduced production of inflammatory cytokines in a time- and dose-dependent manner. Activation of neither IL-1 receptor-associated kinase nor NF-kappaB was observed in macrophages that became tolerant by LPS pretreatment, indicating that the proximal event in Toll-like receptor 4 (TLR4)-MyD88-dependent signaling is affected in tolerant macrophages. Although TLR4 mRNA expression significantly decreased within a few hours of LPS pretreatment and returned to the original level at 24 h, the surface TLR4 expression began to decrease within 1 h, with a gradual decrease after that, and remained suppressed over 24 h. A decrease in inflammatory cytokine production in tolerant macrophages well correlates with down-regulation of the surface TLR4 expression, which may explain one of the mechanisms for LPS tolerance.


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