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利用光学透明技术快速可视化脑组织中的神经元。

Quick visualization of neurons in brain tissues using an optical clearing technique.

作者信息

Sato Yu, Miyawaki Takeyuki, Ouchi Ayako, Noguchi Asako, Yamaguchi Shun, Ikegaya Yuji

机构信息

Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.

Department of Morphological Neuroscience, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu City, Gifu, 501-1194, Japan.

出版信息

Anat Sci Int. 2019 Mar;94(2):199-208. doi: 10.1007/s12565-018-00473-z. Epub 2019 Jan 1.

Abstract

Neurons are classified into several morphological types according to the locations of their somata and the branching patterns of their axons and dendrites. Recent studies suggest that these morphological features are related to their physiological properties, including firing characteristics, responses to neuromodulators, and wiring patterns. Therefore, rapid morphological identification of electrophysiologically recorded neurons promises to advance our understanding of neuronal circuits. One of the most common anatomical cell identification methods is neuronal reconstruction with biocytin delivered through whole-cell patch-clamp pipettes. However, conventional reconstruction methods usually take longer than 24 h and limit the throughput of electrophysiological experiments. Here, we developed a quick, simple cell reconstruction method by optimizing the tissue clearing protocol ScaleSQ. We found that adding 200 mM NaCl almost entirely prevented tissue swelling without compromising optical clearing ability. This solution, termed IsoScaleSQ, allowed us to increase the transparency of the gray matter of 500-µm-thick slices within 30 min, meaning that the total time required to reconstruct whole-cell recorded neurons was reduced to 1 h. This novel method will improve the efficacy and effectiveness of electrophysiological experiments linked to cell morphology.

摘要

神经元根据其胞体位置以及轴突和树突的分支模式被分为几种形态类型。最近的研究表明,这些形态特征与其生理特性相关,包括放电特性、对神经调质的反应以及连接模式。因此,对通过电生理记录的神经元进行快速形态学识别有望促进我们对神经回路的理解。最常见的解剖学细胞识别方法之一是通过全细胞膜片钳移液管注入生物胞素进行神经元重建。然而,传统的重建方法通常需要超过24小时,限制了电生理实验的通量。在这里,我们通过优化组织透明化方案ScaleSQ开发了一种快速、简单的细胞重建方法。我们发现添加200 mM氯化钠几乎完全防止了组织肿胀,同时不影响光学透明能力。这种溶液称为IsoScaleSQ,使我们能够在30分钟内提高500微米厚切片灰质的透明度,这意味着重建全细胞记录神经元所需的总时间减少到1小时。这种新方法将提高与细胞形态相关的电生理实验的效率和效果。

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