Zhang Shiliang, Morales Marisela
National Institute on Drug Abuse, Intramural Research Program, Confocal and Electron Microscopy Core, Baltimore, Maryland.
National Institute on Drug Abuse, Intramural Research Program, Neuronal Networks Section, Baltimore, Maryland.
Curr Protoc Neurosci. 2019 Jun;88(1):e70. doi: 10.1002/cpns.70.
At the ultrastructural level, axon terminals containing synaptic vesicles are clearly observed. These axon terminals (presynaptic component of a synapse) may be seen establishing contacts (synapses) with cell bodies, axons, or dendrites (postsynaptic component of a synapse). By a combination of ultrastructural analysis and immunodetection of molecules, it is possible to determine the subcellular distribution of specific cellular markers (i.e., enzymes), neurotransmitters (within synaptic vesicles), vesicular transporters (in association with vesicles), and receptors (within the presynaptic or postsynaptic component of a synapse). Here we will provide detailed protocols that facilitate the ultrastructural detection of cellular markers, receptors, and vesicular transporters. These protocols include brain ultrastructural immunodetection of one, two, or three different types of molecules prior to brain tissue processing for ultrastructural analysis (pre-embedding immunolabeling), brain molecular immunodetection after tissue processing for ultrastructural analysis (post-embedding immunolabeling), or molecular immunodetection in purified synaptic vesicles. Published 2019. This article is a US Government work and is in the public domain in the USA.
在超微结构水平上,可以清晰地观察到含有突触小泡的轴突终末。这些轴突终末(突触的突触前成分)可见与细胞体、轴突或树突(突触的突触后成分)建立联系(突触)。通过超微结构分析和分子免疫检测相结合的方法,能够确定特定细胞标志物(如酶)、神经递质(在突触小泡内)、囊泡转运体(与囊泡相关)以及受体(在突触的突触前或突触后成分内)的亚细胞分布。在此,我们将提供详细的实验方案,以促进对细胞标志物、受体和囊泡转运体的超微结构检测。这些方案包括在脑组织进行超微结构分析处理之前对一、二或三种不同类型分子进行脑超微结构免疫检测(包埋前免疫标记)、在脑组织进行超微结构分析处理之后进行脑分子免疫检测(包埋后免疫标记),或在纯化的突触小泡中进行分子免疫检测。2019年发表。本文为美国政府作品,在美国属于公共领域。