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用于突触前检测的激光显微手术。

Laser microsurgery for presynaptic interrogation.

作者信息

Wong Hovy Ho-Wai, Watt Alanna J, Sjöström P Jesper

机构信息

Centre for Research in Neuroscience, Brain Repair and Integrative Neuroscience Program, Department of Neurology and Neurosurgery, Department of Medicine, The Research Institute of the McGill University Health Centre, Montreal General Hospital, Montreal, Quebec, Canada.

School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.

出版信息

Nat Protoc. 2025 Feb 7. doi: 10.1038/s41596-024-01125-5.

Abstract

Synaptic connections among neurons are critical for information processing and memory storage in the brain, making them hotspots for neuropathologies. Understanding the physiology of synapses, therefore, may facilitate the development of therapeutic approaches. However, synapses are micrometer-sized functional structures involved in many neuronal processes, where the challenge is deciphering differential signaling in presynaptic and postsynaptic compartments of relatively intact microcircuits. Here we developed a method combining two-photon laser microsurgery with compartment-specific electrophysiological activation and readout to improve the specificity with which neuronal signaling is detected. After finding a connection, femtosecond laser pulses are used to sever the presynaptic axon from the cell body with micrometer precision. This microdissection method is effective to a depth of at least 100 µm. The initial segment of the isolated axon is extracellularly stimulated and activated to release neurotransmitters, as detected via a recipient whole-cell neuron, which is being recorded. This methodology is an alternative to axonal patch-clamp recordings, which are short-lasting and difficult. Together with pharmacology and genetic manipulation, our approach allows the interrogation of compartmentalized signaling in intact synapses. The total time of laser exposure is a few seconds and the microsurgery takes 5-10 min, which enables the interrogation of multiple synapses within an experiment. Our protocol provides a tool to investigate compartment-specific signaling in relatively intact brain tissue, enabling a more comprehensive understanding of neuronal synapses.

摘要

神经元之间的突触连接对于大脑中的信息处理和记忆存储至关重要,使其成为神经病理学的热点。因此,了解突触的生理学可能有助于开发治疗方法。然而,突触是参与许多神经元过程的微米级功能结构,挑战在于解读相对完整的微回路中突触前和突触后区室的差异信号。在这里,我们开发了一种将双光子激光显微手术与区室特异性电生理激活和读出相结合的方法,以提高检测神经元信号的特异性。找到连接后,使用飞秒激光脉冲以微米精度将突触前轴突与细胞体切断。这种显微切割方法在至少100 µm的深度内有效。分离轴突的起始段在细胞外被刺激并激活以释放神经递质,这通过正在记录的受体全细胞神经元进行检测。这种方法是轴突膜片钳记录的一种替代方法,轴突膜片钳记录持续时间短且困难。与药理学和基因操作一起,我们的方法允许对完整突触中的区室化信号进行研究。激光暴露的总时间为几秒钟,显微手术需要5 - 10分钟,这使得在一个实验中能够研究多个突触。我们的方案提供了一种工具,用于研究相对完整的脑组织中区室特异性信号,从而更全面地了解神经元突触。

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