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时间依赖性和选择性小胶质细胞介导的神经性疼痛中脊髓突触的消除。

Time-dependent and selective microglia-mediated removal of spinal synapses in neuropathic pain.

机构信息

Department of Pharmacology and Therapeutics, McGill University, Montréal, QC H3G 1Y6, Canada; Alan Edwards Centre for Research on Pain, McGill University, Montréal, QC H3A 2B4, Canada.

Department of Pharmacology and Therapeutics, McGill University, Montréal, QC H3G 1Y6, Canada.

出版信息

Cell Rep. 2023 Jan 31;42(1):112010. doi: 10.1016/j.celrep.2023.112010. Epub 2023 Jan 18.

Abstract

Neuropathic pain is a debilitating condition resulting from damage to the nervous system. Imbalance of spinal excitation and inhibition has been proposed to contribute to neuropathic pain. However, the structural basis of this imbalance remains unknown. Using a preclinical model of neuropathic pain, we show that microglia selectively engulf spinal synapses that are formed by central neurons and spare those of peripheral sensory neurons. Furthermore, we reveal that removal of inhibitory and excitatory synapses exhibits distinct temporal patterns, in which microglia-mediated inhibitory synapse removal precedes excitatory synapse removal. We also find selective and gradual increase in complement depositions on dorsal horn synapses that corresponds to the temporal pattern of microglial synapse pruning activity and type-specific synapse loss. Together, these results define a specific role for microglia in the progression of neuropathic pain pathogenesis and implicate these immune cells in structural remodeling of dorsal horn circuitry.

摘要

神经病理性疼痛是一种由神经系统损伤引起的使人虚弱的疾病。脊髓兴奋和抑制失衡被认为是导致神经病理性疼痛的原因之一。然而,这种失衡的结构基础尚不清楚。本研究使用神经病理性疼痛的临床前模型,结果表明小胶质细胞选择性吞噬由中枢神经元形成的脊髓突触,而不吞噬外周感觉神经元形成的脊髓突触。此外,研究揭示了抑制性和兴奋性突触的去除具有不同的时间模式,其中小胶质细胞介导的抑制性突触去除先于兴奋性突触去除。研究还发现,在背角突触上,补体沉积呈现选择性和逐渐增加,这与小胶质细胞突触修剪活动和特定类型突触丢失的时间模式相对应。综上所述,这些结果定义了小胶质细胞在神经病理性疼痛发病机制进展中的特定作用,并表明这些免疫细胞参与了背角回路的结构重塑。

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