Regulation of Toll-like receptor signaling pathways in innate immune responses

被引:119
作者
Qian, Cheng [1 ,2 ]
Cao, Xuetao [1 ,2 ,3 ,4 ]
机构
[1] Second Mil Med Univ, Natl Key Lab Med Immunol, Shanghai 200433, Peoples R China
[2] Second Mil Med Univ, Inst Immunol, Shanghai 200433, Peoples R China
[3] Chinese Acad Med Sci, Natl Key Lab Med Mol Biol, Beijing 100730, Peoples R China
[4] Chinese Acad Med Sci, Dept Immunol, Beijing 100730, Peoples R China
来源
TRANSLATIONAL IMMUNOLOGY IN ASIA-OCEANIA | 2013年 / 1283卷
基金
中国国家自然科学基金;
关键词
TLR signaling; immune regulation; innate immunity; inflammation; TRIGGERED INFLAMMATORY RESPONSES; PATTERN-RECOGNITION RECEPTORS; I INTERFERON; NEGATIVE REGULATOR; DEGRADATION; MOLECULES; AUTOIMMUNE; ENDOTOXIN; CROSSTALK; SENSOR;
D O I
10.1111/j.1749-6632.2012.06786.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Toll-like receptors (TLRs) are critical pattern recognition receptors (PRRs) that recognize pathogen-associated molecular patterns (PAMPs), which are conserved and specific molecular "signatures" expressed by pathogens. TLR ligation triggers distinct but shared signaling pathways that lead to effector mechanisms in innate immune responses. TLR specificity and activation are strictly and finely tuned at multiple levels of various signal transduction pathways, resulting in complex signaling platforms. Many molecules, ranging from membrane and cytosol to nuclear, contribute to TLR ligand discrimination or receptor signaling and play different roles in the regulation of TLR responses via different mechanisms, such as cross-regulation, protein modification, helper cofactors, and posttranscriptional and epigenetic regulation. Herein, we summarize the most recent literature that provides new insight into regulation of TLR signaling-triggered innate immune responses. A greater understanding of the mechanisms underlying the control of TLR signaling may provide new targets for therapeutic intervention for infections and inflammatory diseases.
引用
收藏
页码:67 / 74
页数:8
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