背根神经节神经元类型及其功能特化

E. Emery, P. Ernfors
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引用次数: 37

摘要

背根神经节(DRG)的初级感觉神经元反应和传递感觉,如触觉、疼痛、温度、瘙痒等。区分不同类型刺激的能力反映在专门的DRG神经元对特定刺激做出反应的存在上。正因为如此,DRG神经元的全面分类对于准确确定体感如何工作以及提供对慢性疼痛中涉及的细胞类型的见解至关重要。本文从已知功能和基于基因表达谱的预测功能两方面综述了DRG神经元分子类型无偏分类的最新进展。结果表明,感觉神经元具有3种冷敏感神经元类型、5种机械-热敏伤害感受器类型、4种a -低阈值机械感受器类型、5种瘙痒-机械-热敏伤害感受器类型和1种c -低阈值机械感受器类型的基本结构,且分子神经元类型与功能类型之间存在较强的相关性。作为一般特征,每种神经元类型都显示出独特的可预测的响应概况;同时,大多数神经元类型传递多种模态和强度。因此,感觉可能是由活跃的主要传入类型的集合的总和决定的。新的分类方案将在确定躯体感觉的确切细胞和分子机制方面具有指导意义,有助于制定合理的策略来确定慢性疼痛的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dorsal Root Ganglion Neuron Types and Their Functional Specialization
Primary sensory neurons of the dorsal root ganglion (DRG) respond and relay sensations that are felt, such as those for touch, pain, temperature, itch, and more. The ability to discriminate between the various types of stimuli is reflected by the existence of specialized DRG neurons tuned to respond to specific stimuli. Because of this, a comprehensive classification of DRG neurons is critical for determining exactly how somatosensation works and for providing insights into cell types involved during chronic pain. This article reviews the recent advances in unbiased classification of molecular types of DRG neurons in the perspective of known functions as well as predicted functions based on gene expression profiles. The data show that sensory neurons are organized in a basal structure of three cold-sensitive neuron types, five mechano-heat sensitive nociceptor types, four A-Low threshold mechanoreceptor types, five itch-mechano-heat–sensitive nociceptor types and a single C–low-threshold mechanoreceptor type with a strong relation between molecular neuron types and functional types. As a general feature, each neuron type displays a unique and predicable response profile; at the same time, most neuron types convey multiple modalities and intensities. Therefore, sensation is likely determined by the summation of ensembles of active primary afferent types. The new classification scheme will be instructive in determining the exact cellular and molecular mechanisms underlying somatosensation, facilitating the development of rational strategies to identify causes for chronic pain.
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