外域
TLR4型
小胶质细胞
神经科学
受体
Toll样受体
信号转导
细胞生物学
炎症
生物
免疫系统
先天免疫系统
免疫学
医学
内科学
作者
Kelly Bruno,Sarah A. Woller,Yury I. Miller,Tony L. Yaksh,Mark Wallace,Graham Beaton,Krishnan Chakravarthy
出处
期刊:Pain
[Lippincott Williams & Wilkins]
日期:2018-06-07
卷期号:159 (10): 1908-1915
被引量:88
标识
DOI:10.1097/j.pain.0000000000001306
摘要
Toll-like receptors (TLRs) are a family of pattern recognition receptors that initiate signaling in innate and adaptive immune pathways. The highly conserved family of transmembrane proteins comprises an extracellular domain that recognizes exogenous and endogenous danger molecules and an ectodomain that activates downstream pathways in response. Recent studies suggest that continuous activation or dysregulation of TLR signaling may contribute to chronic disease states. The receptor is located not only on inflammatory cells (meningeal and peripheral macrophages) but on neuraxial glia (microglia and astrocytes), Schwann cells, fibroblasts, dorsal root ganglia, and dorsal horn neurons. Procedures blocking TLR functionality have shown pronounced effects on pain behavior otherwise observed in models of chronic inflammation and nerve injury. This review addresses the role of TLR4 as an emerging therapeutic target for the evolution of persistent pain and its role in noncanonical signaling, mediating anomalous pro-algesic actions of opiates. Accordingly, molecules targeting inhibition of this receptor have promise as disease-modifying and opioid-sparing alternatives for persistent pain states.
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