Essential role of MD-2 in LPS responsiveness and TLR4 distribution

被引:0
|
作者
Yoshinori Nagai
Sachiko Akashi
Masakazu Nagafuku
Masato Ogata
Yoichiro Iwakura
Shizuo Akira
Toshio Kitamura
Atsushi Kosugi
Masao Kimoto
Kensuke Miyake
机构
[1] The Institute of Medical Science,Division of Infectious Genetics
[2] The University of Tokyo,Department of Immunology
[3] CREST,Department of Oncogenesis
[4] Japan Science and Technology Corporation,Division of Cellular Therapy
[5] Saga Medical School,undefined
[6] School of Allied Health Sciences,undefined
[7] Faculty of Medicine,undefined
[8] Osaka University Medical School,undefined
[9] The Center for Experimental Medicine,undefined
[10] The Institute of Medical Science,undefined
[11] The University of Tokyo,undefined
[12] Research Institute for Microbial Diseases,undefined
[13] Osaka University,undefined
[14] The Institute of Medical Science,undefined
[15] The University of Tokyo,undefined
来源
Nature Immunology | 2002年 / 3卷
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学科分类号
摘要
Toll-like receptor 4 (TLR4) mediates lipopolysaccharide (LPS) signaling in a variety of cell types. MD-2 is associated with the extracellular domain of TLR4 and augments TLR4-dependent LPS responses in vitro. We show here that MD-2−/− mice do not respond to LPS, do survive endotoxic shock but are susceptible to Salmonella typhimurium infection. We found that in MD-2−/− embryonic fibroblasts, TLR4 was not able to reach the plasma membrane and predominantly resided in the Golgi apparatus, whereas TLR4 was distributed at the leading edge surface of cells in wild-type embryonic fibroblasts. Thus, MD-2 is essential for correct intracellular distribution and LPS-recognition of TLR4.
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页码:667 / 672
页数:5
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