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Emerging role of Toll-like receptors in the control of pain and itch

机译:Toll样受体在控制疼痛和瘙痒中的新兴作用

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摘要

Toll-like receptors (TLRs) are germline-encoded pattern-recognition receptors that initiate innate immune responses by recognizing molecular structures shared by a wide range of pathogens, known as pathogen-associated molecular patterns (PAMPs). After tissue injury or cellular stress, TLRs also detect endogenous ligands known as danger-associated molecular patterns (DAMPs). TLRs are expressed in both non-neuronal and neuronal cell types in the central nervous system (CNS) and contribute to both infectious and non-infectious disorders in the CNS. Following tissue insult and nerve injury, TLRs (such as TLR2, TLR3, and TLR4) induce the activation of microglia and astrocytes and the production of the proinflammatory cytokines in the spinal cord, leading to the development and maintenance of inflammatory pain and neuropathic pain. In particular, primary sensory neurons, such as nociceptors, express TLRs (e.g., TLR4 and TLR7) to sense exogenous PAMPs and endogenous DAMPs released after tissue injury and cellular stress. These neuronal TLRs are new players in the processing of pain and itch by increasing the excitability of primary sensory neurons. Given the prevalence of chronic pain and itch and the suffering of affected people, insights into TLR signaling in the nervous system will open a new avenue for the management of clinical pain and itch.
机译:Toll样受体(TLR)是种系编码的模式识别受体,通过识别多种病原体共有的分子结构(称为病原体相关分子模式(PAMPs))来启动先天性免疫应答。在组织损伤或细胞应激后,TLR还检测内源性配体,称为危险相关分子模式(DAMP)。 TLRs在中枢神经系统(CNS)的非神经元和神经元细胞类型中都有表达,并且在CNS中导致传染性和非传染性疾病。组织损伤和神经损伤后,TLR(例如TLR2,TLR3和TLR4)诱导小胶质细胞和星形胶质细胞的活化以及脊髓中促炎性细胞因子的产生,从而导致炎性疼痛和神经性疼痛的发生和维持。尤其是,主要的感觉神经元,例如伤害感受器,表达TLR(例如TLR4和TLR7),以感知组织损伤和细胞应激后释放的外源PAMP和内源DAMP。这些神经元TLR通过增加初级感觉神经元的兴奋性成为疼痛和瘙痒处理的新参与者。考虑到慢性疼痛和瘙痒的普遍存在以及受影响人群的痛苦,对神经系统中TLR信号传导的见解将为临床管理疼痛和瘙痒开辟新的途径。

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