Department of Cell and Molecular Biology.
Department of Cell and Molecular Biology
J Neurosci. 2020 Jun 24;40(26):4972-4980. doi: 10.1523/JNEUROSCI.2945-19.2020. Epub 2020 May 19.
Synaptic vesicles need to be recycled and refilled rapidly to maintain high-frequency synaptic transmission. However, little is known about the control of neurotransmitter transport into synaptic vesicles, which determines the contents of synaptic vesicles and the strength of synaptic transmission. Here, we report that Na substantially accumulated in the calyx of Held terminals of juvenile mice of either sex during high-frequency spiking. The activity-induced elevation of cytosolic Na activated vesicular Na/H exchanger, facilitated glutamate loading into synaptic vesicles, and increased quantal size of asynchronous released vesicles but did not affect the vesicle pool size or release probability. Consequently, presynaptic Na increased the EPSCs and was required to maintain the reliable high-frequency signal transmission from the presynaptic calyces to the postsynaptic medial nucleus of the trapezoid body (MNTB) neurons. Blocking Na/H exchange activity decreased the postsynaptic current and caused failures in postsynaptic firing. Therefore, during high-frequency synaptic transmission, when large amounts of glutamate are released, Na accumulated in the terminals, activated vesicular Na/H exchanger, and regulated glutamate loading as a function of the level of vesicle release. Auditory information is encoded by action potentials (APs) phase-locked to sound frequency at high rates. A large number of synaptic vesicles are released during high-frequency synaptic transmission; accordingly, synaptic vesicles need to be recycled and refilled rapidly. We have recently found that a Na/H exchanger expressed on synaptic vesicles promotes vesicle filling with glutamate. Here, we showed that when a large number of synaptic vesicles are released during high-frequency synaptic transmission, Na accumulates in axon terminals and facilitates glutamate uptake into synaptic vesicles. Na thus accelerates vesicle replenishment and sustains reliable synaptic transmission.
突触小泡需要快速回收和再填充以维持高频突触传递。然而,对于控制神经递质向突触小泡内运输的机制知之甚少,而该机制决定了突触小泡的内容物和突触传递的强度。在这里,我们报告在雄性和雌性幼鼠的 Held 终球中,高频放电期间大量 Na 在终球内积聚。活性诱导的胞质 Na 升高激活了囊泡 Na/H 交换体,促进了谷氨酸向突触小泡的装载,并增加了异步释放囊泡的量子大小,但不影响囊泡库大小或释放概率。因此,突触前 Na 增加了 EPSC,并需要维持来自突触前终球到梯形体中内侧核(MNTB)神经元的可靠高频信号传递。阻断 Na/H 交换活性会降低突触后电流,并导致突触后放电失败。因此,在高频突触传递期间,当大量谷氨酸释放时,Na 在终球内积聚,激活囊泡 Na/H 交换体,并根据囊泡释放的水平调节谷氨酸的装载。听觉信息通过与声音频率锁相的动作电位(APs)以高频率编码。在高频突触传递期间会释放大量的突触小泡;因此,需要快速回收和再填充突触小泡。我们最近发现,表达在突触小泡上的 Na/H 交换体促进了谷氨酸与小泡的结合。在这里,我们表明,在高频突触传递期间大量释放突触小泡时,Na 在轴突末梢内积聚并促进谷氨酸摄取到突触小泡中。因此,Na 加速了囊泡的补充并维持了可靠的突触传递。