Department of Biology, The Picower Institute for Learning and Memory, Massachusetts Institute of Technology (MIT), Bldg. 46-3243, 43 Vassar St., Cambridge, MA, 02139, USA.
Department of Brain and Cognitive Sciences, The Picower Institute for Learning and Memory, Massachusetts Institute of Technology (MIT), Bldg. 46-3243, 43 Vassar St., Cambridge, MA, 02139, USA.
Cell Mol Life Sci. 2021 May;78(9):4335-4364. doi: 10.1007/s00018-021-03788-9. Epub 2021 Feb 22.
The Synaptotagmin (SYT) family of proteins play key roles in regulating membrane trafficking at neuronal synapses. Using both Ca-dependent and Ca-independent interactions, several SYT isoforms participate in synchronous and asynchronous fusion of synaptic vesicles (SVs) while preventing spontaneous release that occurs in the absence of stimulation. Changes in the function or abundance of the SYT1 and SYT7 isoforms alter the number and route by which SVs fuse at nerve terminals. Several SYT family members also regulate trafficking of other subcellular organelles at synapses, including dense core vesicles (DCV), exosomes, and postsynaptic vesicles. Although SYTs are linked to trafficking of multiple classes of synaptic membrane compartments, how and when they interact with lipids, the SNARE machinery and other release effectors are still being elucidated. Given mutations in the SYT family cause disorders in both the central and peripheral nervous system in humans, ongoing efforts are defining how these proteins regulate vesicle trafficking within distinct neuronal compartments. Here, we review the Drosophila SYT family and examine their role in synaptic communication. Studies in this invertebrate model have revealed key similarities and several differences with the predicted activity of their mammalian counterparts. In addition, we highlight the remaining areas of uncertainty in the field and describe outstanding questions on how the SYT family regulates membrane trafficking at nerve terminals.
突触结合蛋白(SYT)家族的蛋白在调节神经元突触的膜转运中发挥着关键作用。通过 Ca 依赖性和非依赖性相互作用,几种 SYT 异构体参与突触小泡(SV)的同步和异步融合,同时防止在没有刺激的情况下发生的自发释放。SYT1 和 SYT7 异构体的功能或丰度的变化改变了 SV 在神经末梢融合的数量和途径。几种 SYT 家族成员还调节突触处其他亚细胞细胞器的运输,包括致密核心囊泡(DCV)、外泌体和突触后囊泡。尽管 SYTs 与多种类型的突触膜隔室的转运有关,但它们如何以及何时与脂质、SNARE 机制和其他释放效应器相互作用仍在阐明之中。鉴于 SYT 家族的突变会导致人类中枢和周围神经系统的疾病,目前正在努力定义这些蛋白如何在不同的神经元隔室中调节囊泡转运。在这里,我们回顾了果蝇 SYT 家族,并研究了它们在突触通讯中的作用。在这个无脊椎动物模型中的研究揭示了与它们的哺乳动物对应物的预测活性的关键相似性和几个差异。此外,我们还强调了该领域中仍然存在的不确定性,并描述了关于 SYT 家族如何调节神经末梢处的膜转运的悬而未决的问题。