Department of Life Science, University of Trieste, via Giorgieri 5, 34127, Trieste, Italy.
Brain Res Bull. 2019 Sep;151:119-124. doi: 10.1016/j.brainresbull.2018.12.020. Epub 2019 Jan 17.
Peripheral stimuli are transduced by specific receptors expressed by sensory neurons and are further processed in the dorsal horn of spinal cord before to be transmitted to the brain. While relative few receptor subtypes mediate the initial depolarisation of sensory neurons, an impressive number of molecules and ion channels integrate these inputs into coded signals. Soluble mediators and ambient conditions further shape these processes, potentially triggering peripheral and central sensitisation, or sensory downregulation. Extracellular ATP is a major signaling molecule that acts via purinergic receptors and is a powerful modulator of cell communication as well as a neurotransmitter at peripheral/central synapses. In particular, ATP-mediated signals are transduced by P2X3 receptors expressed mainly by peripheral sensory neurons. Recent evidence suggests that P2X3 receptor function not only induces neuron depolarisation and firing with consequent neurotransmitter release, but it also triggers intracellular molecular changes that amplify purinergic signaling with important consequences.
外周刺激通过感觉神经元表达的特定受体转导,然后在脊髓背角进一步处理,再被传递到大脑。虽然相对较少的受体亚型介导感觉神经元的初始去极化,但大量的分子和离子通道将这些输入整合为编码信号。可溶性介质和环境条件进一步塑造这些过程,可能引发外周和中枢敏化或感觉下调。细胞外 ATP 是一种主要的信号分子,通过嘌呤能受体发挥作用,是细胞通讯的强大调节剂,也是外周/中枢突触的神经递质。特别是,ATP 介导的信号由主要在外周感觉神经元中表达的 P2X3 受体转导。最近的证据表明,P2X3 受体功能不仅诱导神经元去极化和放电,从而导致神经递质释放,还触发细胞内分子变化,放大嘌呤能信号,产生重要后果。