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从蝌蚪神经元中进行原位全细胞膜片钳记录。

Making In Situ Whole-Cell Patch-Clamp Recordings from Tadpole Neurons.

机构信息

School of Psychology and Neuroscience, St Andrews, Fife, KY16 9TS, United Kingdom

出版信息

Cold Spring Harb Protoc. 2021 Oct 1;2021(10):pdb.prot106856. doi: 10.1101/pdb.prot106856.

Abstract

tadpoles have been an excellent, simple vertebrate model for studying the basic organization and physiology of the spinal cord and motor centers in the brainstem. In the past, intracellular recordings from the spinal and brainstem neurons were primarily made using sharp electrodes, although whole-cell patch-clamp technology has been around since the early 1980s. In this protocol, I describe the dissections and procedures needed for in situ whole-cell patch-clamp recording, which has become routine in tadpole neurophysiology since the early 2000s. The critical step in the dissections is to delicately remove some ependymal cells lining the tadpole neurocoele in order to expose clean neuronal somata without severing axon tracts. Whole-cell recordings can then be made from the somata in either current- or voltage-clamp mode.

摘要

蝌蚪一直是研究脊髓和脑干运动中枢基本组织和生理学的极佳的、简单的脊椎动物模型。过去,主要使用尖锐电极从脊髓和脑干神经元中进行细胞内记录,尽管全细胞膜片钳技术自 20 世纪 80 年代初就已问世。在本方案中,我描述了原位全细胞膜片钳记录所需的解剖和程序,自 21 世纪初以来,该技术已成为蝌蚪神经生理学中的常规方法。解剖过程中的关键步骤是小心地去除一些覆盖在蝌蚪神经腔中的室管膜细胞,以便在不切断轴突束的情况下暴露干净的神经元胞体。然后可以在电流或电压钳模式下从胞体上进行全细胞膜片钳记录。

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