Sneve Madison A, Piatkevich Kiryl D
Department of Brain and Cognitive Sciences, MIT, Cambridge, MA, United States.
School of Life Sciences, Westlake University, Hangzhou, China.
Front Synaptic Neurosci. 2022 Jan 18;13:754814. doi: 10.3389/fnsyn.2021.754814. eCollection 2021.
Mapping and determining the molecular identity of individual synapses is a crucial step towards the comprehensive reconstruction of neuronal circuits. Throughout the history of neuroscience, microscopy has been a key technology for mapping brain circuits. However, subdiffraction size and high density of synapses in brain tissue make this process extremely challenging. Electron microscopy (EM), with its nanoscale resolution, offers one approach to this challenge yet comes with many practical limitations, and to date has only been used in very small samples such as , tadpole larvae, fruit fly brain, or very small pieces of mammalian brain tissue. Moreover, EM datasets require tedious data tracing. Light microscopy in combination with tissue expansion physical magnification-known as expansion microscopy (ExM)-offers an alternative approach to this problem. ExM enables nanoscale imaging of large biological samples, which in combination with multicolor neuronal and synaptic labeling offers the unprecedented capability to trace and map entire neuronal circuits in fully automated mode. Recent advances in new methods for synaptic staining as well as new types of optical molecular probes with superior stability, specificity, and brightness provide new modalities for studying brain circuits. Here we review advanced methods and molecular probes for fluorescence staining of the synapses in the brain that are compatible with currently available expansion microscopy techniques. In particular, we will describe genetically encoded probes for synaptic labeling in mice, zebrafish, fruit flies, and , which enable the visualization of post-synaptic scaffolds and receptors, presynaptic terminals and vesicles, and even a snapshot of the synaptic activity itself. We will address current methods for applying these probes in ExM experiments, as well as appropriate vectors for the delivery of these molecular constructs. In addition, we offer experimental considerations and limitations for using each of these tools as well as our perspective on emerging tools.
绘制并确定单个突触的分子特性是全面重建神经回路的关键一步。在神经科学的发展历程中,显微镜技术一直是绘制脑回路的关键技术。然而,脑组织中突触的亚衍射尺寸和高密度使得这一过程极具挑战性。电子显微镜(EM)具有纳米级分辨率,为应对这一挑战提供了一种方法,但也存在许多实际限制,迄今为止仅用于非常小的样本,如蝌蚪幼虫、果蝇大脑或非常小的哺乳动物脑组织切片。此外,EM数据集需要繁琐的数据追踪。结合组织扩张(物理放大)的光学显微镜——即扩张显微镜(ExM)——为解决这一问题提供了另一种方法。ExM能够对大型生物样本进行纳米级成像,与多色神经元和突触标记相结合,提供了以前所未有的能力以全自动模式追踪和绘制整个神经回路。突触染色新方法以及具有卓越稳定性、特异性和亮度的新型光学分子探针的最新进展为研究脑回路提供了新的模式。在这里,我们综述了与目前可用的扩张显微镜技术兼容的用于脑内突触荧光染色的先进方法和分子探针。特别是,我们将描述用于小鼠、斑马鱼、果蝇等突触标记的基因编码探针,这些探针能够可视化突触后支架和受体、突触前终末和囊泡,甚至突触活动本身的快照。我们将讨论在ExM实验中应用这些探针的当前方法,以及用于递送这些分子构建体的合适载体。此外,我们还提供了使用这些工具的实验注意事项和局限性,以及我们对新兴工具的看法。