Guzikowski Natalie J, Kavalali Ege T
Department of Pharmacology, Vanderbilt University, Nashville, TN, United States.
Vanderbilt Brain Institute, Vanderbilt University, Nashville, TN, United States.
Front Synaptic Neurosci. 2021 Dec 22;13:796498. doi: 10.3389/fnsyn.2021.796498. eCollection 2021.
Synapses maintain synchronous, asynchronous, and spontaneous modes of neurotransmission through distinct molecular and biochemical pathways. Traditionally a single synapse was assumed to have a homogeneous organization of molecular components both at the active zone and post-synaptically. However, recent advancements in experimental tools and the further elucidation of the physiological significance of distinct forms of release have challenged this notion. In comparison to rapid evoked release, the physiological significance of both spontaneous and asynchronous neurotransmission has only recently been considered in parallel with synaptic structural organization. Active zone nanostructure aligns with postsynaptic nanostructure creating a precise trans-synaptic alignment of release sites and receptors shaping synaptic efficacy, determining neurotransmission reliability, and tuning plasticity. This review will discuss how studies delineating synaptic nanostructure create a picture of a molecularly heterogeneous active zone tuned to distinct forms of release that may dictate diverse synaptic functional outputs.
突触通过不同的分子和生化途径维持神经传递的同步、异步和自发模式。传统上,人们认为单个突触在活性区和突触后都具有分子成分的均匀组织。然而,实验工具的最新进展以及对不同释放形式生理意义的进一步阐明对这一概念提出了挑战。与快速诱发释放相比,自发和异步神经传递的生理意义直到最近才与突触结构组织一并被考虑。活性区纳米结构与突触后纳米结构对齐,形成释放位点和受体的精确跨突触对齐,塑造突触效能,决定神经传递可靠性,并调节可塑性。本综述将讨论描绘突触纳米结构的研究如何构建一幅分子异质性活性区的图景,该活性区针对不同的释放形式进行调整,可能决定多种突触功能输出。