| Literature DB >> 12433373 |
Reiko Nakagawa1, Tetsuji Naka, Hiroko Tsutsui, Minoru Fujimoto, Akihiro Kimura, Tatsuo Abe, Ekihiro Seki, Shintaro Sato, Osamu Takeuchi, Kiyoshi Takeda, Shizuo Akira, Koichi Yamanishi, Ichirou Kawase, Kenji Nakanishi, Tadamitsu Kishimoto.
Abstract
SOCS-1 is a negative regulatory molecule of the JAK-STAT signal cascade. Here, we demonstrate that SOCS-1 is a critical downregulating factor for LPS signal pathways. SOCS-1 expression was promptly induced in macrophages upon LPS stimulation. SOCS-1-deficient mice were highly sensitive to LPS-induced shock and produced increased levels of inflammatory cytokines. Introduction of SOCS-1 inhibited LPS-induced NF-kappaB and STAT1 activation in macrophages. Furthermore, LPS tolerance, a refractory state to second LPS stimulation, was not observed in SOCS-1-deficient mice. These results suggest SOCS-1 as an essential, negative regulator in LPS responses that protects the host from harmful overresponses to LPS and may provide new insight into the endotoxin-induced fatal syndrome that occasionally occurs following infection.Entities:
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Year: 2002 PMID: 12433373 DOI: 10.1016/s1074-7613(02)00449-1
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745