Fields R Douglas, Burnstock Geoffrey
National Institute of Child Health and Human Development, National Institutes of Health, Building 35, Room 2A211, MSC 3713, 35 Lincoln Drive, Bethesda, Maryland 20892, USA.
Nat Rev Neurosci. 2006 Jun;7(6):423-36. doi: 10.1038/nrn1928.
Activity-dependent release of ATP from synapses, axons and glia activates purinergic membrane receptors that modulate intracellular calcium and cyclic AMP. This enables glia to detect neural activity and communicate among other glial cells by releasing ATP through membrane channels and vesicles. Through purinergic signalling, impulse activity regulates glial proliferation, motility, survival, differentiation and myelination, and facilitates interactions between neurons, and vascular and immune system cells. Interactions among purinergic, growth factor and cytokine signalling regulate synaptic strength, development and responses to injury. We review the involvement of ATP and adenosine receptors in neuron-glia signalling, including the release and hydrolysis of ATP, how the receptors signal, the pharmacological tools used to study them, and their functional significance.
依赖于活动的ATP从突触、轴突和神经胶质细胞释放,激活嘌呤能膜受体,调节细胞内钙和环磷酸腺苷。这使得神经胶质细胞能够检测神经活动,并通过膜通道和囊泡释放ATP在其他神经胶质细胞之间进行通信。通过嘌呤能信号传导,冲动活动调节神经胶质细胞的增殖、运动、存活、分化和髓鞘形成,并促进神经元与血管及免疫系统细胞之间的相互作用。嘌呤能、生长因子和细胞因子信号传导之间的相互作用调节突触强度、发育和对损伤的反应。我们综述了ATP和腺苷受体在神经元-神经胶质细胞信号传导中的作用,包括ATP的释放和水解、受体如何发出信号、用于研究它们的药理学工具及其功能意义。