School of Life Sciences, University of Warwick, United Kingdom.
School of Life Sciences, University of Warwick, United Kingdom.
Neuropharmacology. 2023 May 15;229:109477. doi: 10.1016/j.neuropharm.2023.109477. Epub 2023 Feb 24.
ATP released from the synaptic terminals and astrocytes can activate neuronal P2 receptors at a variety of locations across the CNS. Although the postsynaptic ATP-mediated signalling does not bring a major contribution into the excitatory transmission, it is instrumental for slow and diffuse modulation of synaptic dynamics and neuronal firing in many CNS areas. Neuronal P2X and P2Y receptors can be activated by ATP released from the synaptic terminals, astrocytes and microglia and thereby can participate in the regulation of synaptic homeostasis and plasticity. There is growing evidence of importance of purinergic regulation of synaptic transmission in different physiological and pathological contexts. Here, we review the main mechanisms underlying the complexity and diversity of purinergic signalling and purinergic modulation in central neurons.
从突触末梢和星形胶质细胞释放的 ATP 可以激活中枢神经系统中各种位置的神经元 P2 受体。虽然突触后 ATP 介导的信号传递对兴奋性传递没有重大贡献,但它对于许多中枢神经系统区域的突触动力学和神经元放电的缓慢和弥散调节是至关重要的。神经元 P2X 和 P2Y 受体可以被突触末梢、星形胶质细胞和小胶质细胞释放的 ATP 激活,从而参与调节突触稳态和可塑性。越来越多的证据表明,嘌呤能调节在不同的生理和病理情况下对突触传递的重要性。在这里,我们回顾了中枢神经元中嘌呤能信号传递的复杂性和多样性以及嘌呤能调节的主要机制。