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活体小鼠神经肌肉突触的共聚焦显微内镜检查

Confocal Microendoscopy of Neuromuscular Synapses in Living Mice.

作者信息

Blanco Gonzalo, Ribchester Richard R

机构信息

Department of Biology, University of York, Heslington, York, United Kingdom.

Euan MacDonald Centre for Motor Neurone Disease Research, University of Edinburgh, Edinburgh, United Kingdom.

出版信息

Curr Protoc Mouse Biol. 2012 Mar 1;2(1):1-8. doi: 10.1002/9780470942390.mo110144.

Abstract

Here we describe a step-by-step method for vital imaging of neuromuscular junctions (NMJ) and axons using fiber-optic confocal microendoscopy (CME). A commercially available system, the Cellvizio Lab, can be applied to transgenic mouse lines expressing yellow fluorescent protein in all or pseudorandom sub-subsets of motor neurons. Microscopic imaging in vivo is achieved by means of a flexible optical fiber probe that excites and collects the emitted light from fluorescently labeled structures. The hand-held probe is introduced through small skin incisions to visualize nerves and neuromuscular junctions from superficial muscles. Interpolation software then reconstructs the images in real time. The images are of sufficient quality to permit screening of axonal and neuromuscular synaptic integrity and other aspects of their phenotype in live animals. Curr. Protoc. Mouse Biol. 2:1-8 © 2012 by John Wiley & Sons, Inc.

摘要

在此,我们描述了一种使用光纤共聚焦显微内镜(CME)对神经肌肉接头(NMJ)和轴突进行活体成像的分步方法。一种市售系统Cellvizio Lab,可应用于在所有运动神经元或伪随机亚组运动神经元中表达黄色荧光蛋白的转基因小鼠品系。通过柔性光纤探头激发并收集来自荧光标记结构发出的光,实现体内显微成像。手持探头通过小的皮肤切口插入,以可视化浅表肌肉中的神经和神经肌肉接头。然后,插值软件实时重建图像。这些图像质量足以在活体动物中筛查轴突和神经肌肉突触的完整性及其表型的其他方面。《小鼠生物学实验指南》第2卷:1 - 8页 2012年 约翰威立国际出版公司版权所有

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