Mannose-binding lectin enhances Toll-like receptors 2 and 6 signaling from the phagosome

被引:132
作者
Ip, W. K. Eddie [1 ]
Takahashi, Kazue [1 ]
Moore, Kathryn J. [2 ]
Stuart, Lynda M. [1 ,3 ]
Ezekowitz, R. Alan B. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Pediat, Lab Dev Immunol, Boston, MA 02114 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Lipid Metabolism Unit, Boston, MA 02114 USA
[3] Univ Edinburgh, Ctr Inflammat Res, Edinburgh EH8 9AG, Midlothian, Scotland
基金
英国惠康基金;
关键词
D O I
10.1084/jem.20071164
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Innate immunity is the first-line defense against pathogens and relies on phagocytes, soluble components, and cell-surface and cytosolic pattern recognition receptors. Despite using hard-wired receptors and signaling pathways, the innate immune response demonstrates surprising specificity to different pathogens. We determined how combinatorial use of innate immune defense mechanisms defines the response. We describe a novel cooperation between a soluble component of the innate immune system, the mannose-binding lectin, and Toll-like receptor 2 that both specifies and amplifies the host response to Staphylococcus aureus. Furthermore, we demonstrate that this cooperation occurs within the phagosome, emphasizing the importance of engulfment in providing the appropriate cellular environment to facilitate the synergy between these defense pathways.
引用
收藏
页码:169 / 181
页数:13
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