Below the surface: The inner lives of TLR4 and TLR9

被引:98
作者
Marongiu, Laura [1 ]
Gornati, Laura [1 ]
Artuso, Irene [1 ]
Zanoni, Ivan [1 ,2 ,3 ]
Granucci, Francesca [1 ]
机构
[1] Univ Milano Bicocca, Dept Biotechnol & Biosci, Piazza Sci 2, I-20126 Milan, Italy
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Boston Childrens Hosp, Div Gastroenterol, Boston, MA USA
关键词
innate immunity; autoimmunity; intracellular signaling; receptors trafficking; inflammation; TOLL-LIKE RECEPTORS; I-KAPPA-B; SYSTEMIC-LUPUS-ERYTHEMATOSUS; PLASMACYTOID DENDRITIC CELLS; INTERFERON-ALPHA PRODUCTION; PROTEOLYTIC CLEAVAGE; MURINE MODEL; CPG-DNA; T-CELLS; AUTOANTIBODY PRODUCTION;
D O I
10.1002/JLB.3MIR1218-483RR
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
TLRs are a class of pattern recognition receptors (PRRs) that detect invading microbes by recognizing pathogen-associated molecular patterns (PAMPs). Upon PAMP engagement, TLRs activate a signaling cascade that leads to the production of inflammatory mediators. The localization of TLRs, either on the plasma membrane or in the endolysosomal compartment, has been considered to be a fundamental aspect to determine to which ligands the receptors bind, and which transduction pathways are induced. However, new observations have challenged this view by identifying complex trafficking events that occur upon TLR-ligand binding. These findings have highlighted the central role that endocytosis and receptor trafficking play in the regulation of the innate immune response. Here, we review the TLR4 and TLR9 transduction pathways and the importance of their different subcellular localization during the inflammatory response. Finally, we discuss the implications of TLR9 subcellular localization in autoimmunity.
引用
收藏
页码:147 / 160
页数:14
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