Departments of Neurology and Physiology, Graduate Programs in Neuroscience and Cell Biology, Kavli Institute for Fundamental Neuroscience, Weill Institute for the Neurosciences, UCSF School of Medicine, San Francisco, CA 94143, USA.
Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Neuron. 2019 May 22;102(4):786-800.e5. doi: 10.1016/j.neuron.2019.03.031. Epub 2019 Apr 16.
In contrast to temporal coding by synaptically acting neurotransmitters such as glutamate, neuromodulators such as monoamines signal changes in firing rate. The two modes of signaling have been thought to reflect differences in release by different cells. We now find that midbrain dopamine neurons release glutamate and dopamine with different properties that reflect storage in different synaptic vesicles. The vesicles differ in release probability, coupling to presynaptic Ca channels and frequency dependence. Although previous work has attributed variation in these properties to differences in location or cytoskeletal association of synaptic vesicles, the release of different transmitters shows that intrinsic differences in vesicle identity drive different modes of release. Indeed, dopamine but not glutamate vesicles depend on the adaptor protein AP-3, revealing an unrecognized linkage between the pathway of synaptic vesicle recycling and the properties of exocytosis. Storage of the two transmitters in different vesicles enables the transmission of distinct signals.
与通过突触作用的神经递质(如谷氨酸)进行的时间编码相反,神经调质(如单胺类物质)信号传递放电率的变化。这两种信号传递方式被认为反映了不同细胞释放的差异。我们现在发现,中脑多巴胺神经元以反映不同突触小泡储存的不同特性释放谷氨酸和多巴胺。这些小泡在释放概率、与突触前 Ca 通道的偶联以及频率依赖性方面存在差异。尽管以前的工作将这些特性的变化归因于突触小泡位置或细胞骨架关联的差异,但不同递质的释放表明,小泡身份的内在差异驱动着不同的释放模式。事实上,多巴胺小泡而不是谷氨酸小泡依赖衔接蛋白 AP-3,这揭示了突触小泡再循环途径和胞吐作用特性之间未被认识的联系。两种递质在不同小泡中的储存使不同信号的传递成为可能。