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Mapping Synapses by Conjugate Light-Electron Array Tomography

机译:共轭光电子阵列层析成像的突触映射。

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摘要

Synapses of the mammalian CNS are diverse in size, structure, molecular composition, and function. Synapses in their myriad variations are fundamental to neural circuit development, homeostasis, plasticity, and memory storage. Unfortunately, quantitative analysis and mapping of the brain's heterogeneous synapse populations has been limited by the lack of adequate single-synapse measurement methods. Electron microscopy (EM) is the definitive means to recognize and measure individual synaptic contacts, but EM has only limited abilities to measure the molecular composition of synapses. This report describes conjugate array tomography (AT), a volumetric imaging method that integrates immunofluorescence and EM imaging modalities in voxel-conjugate fashion. We illustrate the use of conjugate AT to advance the proteometric measurement of EM-validated single-synapse analysis in a study of mouse cortex.
机译:哺乳动物中枢神经系统的突触的大小,结构,分子组成和功能各不相同。突触的无数变化是神经回路发展,体内平衡,可塑性和记忆存储的基础。不幸的是,由于缺乏足够的单突触测量方法,对大脑异质突触种群的定量分析和作图受到了限制。电子显微镜(EM)是识别和测量单个突触接触的确定手段,但是EM仅具有有限的能力来测量突触的分子组成。本报告介绍了共轭阵列层析成像(AT),这是一种以体素-共轭方式整合免疫荧光和EM成像方式的体积成像方法。我们在小鼠皮层研究中说明了使用缀合物AT来进行经EM验证的单突触分析的蛋白质计量测量。

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