Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK.
Methods Mol Biol. 2021;2188:243-257. doi: 10.1007/978-1-0716-0818-0_12.
Cultured hippocampal slices from rodents, in which the architecture and functional properties of the hippocampal network are largely preserved, have proved to be a powerful substrate for studying healthy and pathological neuronal mechanisms. Here, we delineate the membrane-interface method for maintaining organotypic slices in culture for several weeks. The protocol includes procedures for dissecting hippocampus from rat brain, and collecting slices using a vibratome. This method provides the experimenter with easy access to both the brain tissue and culture medium, which facilitates genetic and pharmacological manipulations and enables experiments that incorporate imaging and electrophysiology. The method is generally applicable to rats of different ages, and to different brain regions, and can be modified for culture of slices from other species including mice.
原代培养的啮齿动物海马脑片在很大程度上保留了海马网络的结构和功能特性,已被证明是研究健康和病理神经元机制的有力基质。在这里,我们描述了一种用于培养器官型脑片数周的膜-界面方法。该方案包括从大鼠大脑中分离海马体和使用振动切片机收集切片的步骤。该方法为实验者提供了方便进入脑组织和培养液的途径,便于进行基因和药理学操作,并能够进行结合成像和电生理学的实验。该方法通常适用于不同年龄的大鼠和不同的脑区,也可以进行修改以培养包括小鼠在内的其他物种的脑片。