TLR accessory molecules

被引:223
作者
Akashi-Takamura, Sachiko [1 ]
Miyake, Kensuke [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Dept Microbiol & Immunol, Div Infect Genet,Minato Ku, Tokyo 1088639, Japan
关键词
D O I
10.1016/j.coi.2008.07.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Accessory molecules are required for microbial recognition by Toll-like receptor (TLR), subsequent signaling, and regulation of ensuing immune responses. Accessory molecules regulate TLRs on the cell surface (MD-2 and RP105), or in the endoplasmic reticulum (ER) (Unc93B, PRAT4A, and gp96). Other types of accessory molecules modulate TLR responses by acting directly on TLR ligands (CD14, CD36, HMGB1, and the antimicrobial peptide LL37). These molecules cooperate with TLR, inducing appropriate defense mechanisms, It is important to understand how TLR signaling is controlled by these accessory molecules. These accessory molecules could be promising targets for therapeutic intervention in infectious disease and immune disorders.
引用
收藏
页码:420 / 425
页数:6
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