Laser microsurgery for presynaptic interrogation.

IF 13.1 1区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Hovy Ho-Wai Wong, Alanna J Watt, P Jesper Sjöström
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引用次数: 0

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.

突触前探查的激光显微外科。
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,可能会促进治疗方法的发展。然而,突触是微米大小的功能结构,涉及许多神经元过程,其中的挑战是在相对完整的微电路中破译突触前和突触后间隔的差异信号。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。在找到连接后,利用飞秒激光脉冲以微米级的精度将突触前轴突与细胞体分离。这种显微解剖方法在至少100 μ m的深度内是有效的。孤立轴突的起始部分在细胞外被刺激和激活,释放神经递质,这是通过受体全细胞神经元检测到的,并被记录下来。这种方法是替代轴突膜片钳记录,这是短期的和困难的。结合药理学和基因操作,我们的方法可以对完整突触中的区隔信号进行询问。激光照射总时间为几秒,显微手术时间为5-10分钟,可以在一次实验中对多个突触进行检测。我们的方案提供了一种工具来研究相对完整的脑组织中的室特异性信号,从而更全面地了解神经元突触。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nature Protocols
Nature Protocols 生物-生化研究方法
CiteScore
29.10
自引率
0.70%
发文量
128
审稿时长
4 months
期刊介绍: Nature Protocols focuses on publishing protocols used to address significant biological and biomedical science research questions, including methods grounded in physics and chemistry with practical applications to biological problems. The journal caters to a primary audience of research scientists and, as such, exclusively publishes protocols with research applications. Protocols primarily aimed at influencing patient management and treatment decisions are not featured. The specific techniques covered encompass a wide range, including but not limited to: Biochemistry, Cell biology, Cell culture, Chemical modification, Computational biology, Developmental biology, Epigenomics, Genetic analysis, Genetic modification, Genomics, Imaging, Immunology, Isolation, purification, and separation, Lipidomics, Metabolomics, Microbiology, Model organisms, Nanotechnology, Neuroscience, Nucleic-acid-based molecular biology, Pharmacology, Plant biology, Protein analysis, Proteomics, Spectroscopy, Structural biology, Synthetic chemistry, Tissue culture, Toxicology, and Virology.
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