Matsumoto Naoyuki, Yamamoto Nobuhiko
Department of Medical Neuroscience, Graduate School of Medical Sciences, Kanazawa University; Neuroscience Laboratories, Graduate School of Frontier Biosciences, Osaka University.
Neuroscience Laboratories, Graduate School of Frontier Biosciences, Osaka University;
J Vis Exp. 2018 Mar 28(133):56553. doi: 10.3791/56553.
Axon branching and synapse formation are crucial processes for establishing precise neuronal circuits. During development, sensory thalamocortical (TC) axons form branches and synapses in specific layers of the cerebral cortex. Despite the obvious spatial correlation between axon branching and synapse formation, the causal relationship between them is poorly understood. To address this issue, we recently developed a method for simultaneous imaging of branching and synapse formation of individual TC axons in organotypic cocultures. This protocol describes a method which consists of a combination of an organotypic coculture and electroporation. Organotypic cocultures of the thalamus and cerebral cortex facilitate gene manipulation and observation of axonal processes, preserving characteristic structures such as laminar configuration. Two distinct plasmids encoding DsRed and EGFP-tagged synaptophysin (SYP-EGFP) were co-transfected into a small number of thalamic neurons by an electroporation technique. This method allowed us to visualize individual axonal morphologies of TC neurons and their presynaptic sites simultaneously. The method also enabled long-term observation which revealed the causal relationship between axon branching and synapse formation.
轴突分支和突触形成是建立精确神经回路的关键过程。在发育过程中,感觉丘脑皮质(TC)轴突在大脑皮质的特定层形成分支和突触。尽管轴突分支与突触形成之间存在明显的空间相关性,但它们之间的因果关系却知之甚少。为了解决这个问题,我们最近开发了一种方法,用于在器官型共培养中同时成像单个TC轴突的分支和突触形成。本方案描述了一种由器官型共培养和电穿孔相结合的方法。丘脑和大脑皮质的器官型共培养有助于基因操作和轴突过程的观察,保留了诸如层状结构等特征性结构。通过电穿孔技术将两种分别编码DsRed和EGFP标记的突触素(SYP-EGFP)的不同质粒共转染到少数丘脑神经元中。这种方法使我们能够同时可视化TC神经元的单个轴突形态及其突触前位点。该方法还能够进行长期观察,揭示了轴突分支与突触形成之间的因果关系。