Cunningham Karen L, Littleton J Troy
The Picower Institute for Learning and Memory, Department of Biology, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, United States.
Front Mol Neurosci. 2023 Jan 13;15:1116729. doi: 10.3389/fnmol.2022.1116729. eCollection 2022.
Voltage-gated Ca channels (VGCCs) mediate Ca influx to trigger neurotransmitter release at specialized presynaptic sites termed active zones (AZs). The abundance of VGCCs at AZs regulates neurotransmitter release probability ( ), a key presynaptic determinant of synaptic strength. Given this functional significance, defining the processes that cooperate to establish AZ VGCC abundance is critical for understanding how these mechanisms set synaptic strength and how they might be regulated to control presynaptic plasticity. VGCC abundance at AZs involves multiple steps, including channel biosynthesis (transcription, translation, and trafficking through the endomembrane system), forward axonal trafficking and delivery to synaptic terminals, incorporation and retention at presynaptic sites, and protein recycling. Here we discuss mechanisms that control VGCC abundance at synapses, highlighting findings from invertebrate and vertebrate models.
电压门控钙通道(VGCCs)介导钙离子内流,从而在称为活性区(AZs)的特殊突触前位点触发神经递质释放。活性区的电压门控钙通道丰度调节神经递质释放概率(),这是突触强度的一个关键突触前决定因素。鉴于其功能重要性,确定协同建立活性区电压门控钙通道丰度的过程对于理解这些机制如何设定突触强度以及如何对其进行调节以控制突触前可塑性至关重要。活性区的电压门控钙通道丰度涉及多个步骤,包括通道生物合成(转录、翻译以及通过内膜系统的运输)、正向轴突运输并递送至突触终末、在突触前位点的整合与保留以及蛋白质循环利用。在此,我们讨论控制突触处电压门控钙通道丰度的机制,并重点介绍来自无脊椎动物和脊椎动物模型的研究结果。