Ting Jonathan T, Lee Brian R, Chong Peter, Soler-Llavina Gilberto, Cobbs Charles, Koch Christof, Zeng Hongkui, Lein Ed
Cell Types Program, Allen Institute for Brain Science;
Cell Types Program, Allen Institute for Brain Science.
J Vis Exp. 2018 Feb 26(132):53825. doi: 10.3791/53825.
This protocol is a practical guide to the N-methyl-D-glucamine (NMDG) protective recovery method of brain slice preparation. Numerous recent studies have validated the utility of this method for enhancing neuronal preservation and overall brain slice viability. The implementation of this technique by early adopters has facilitated detailed investigations into brain function using diverse experimental applications and spanning a wide range of animal ages, brain regions, and cell types. Steps are outlined for carrying out the protective recovery brain slice technique using an optimized NMDG artificial cerebrospinal fluid (aCSF) media formulation and enhanced procedure to reliably obtain healthy brain slices for patch clamp electrophysiology. With this updated approach, a substantial improvement is observed in the speed and reliability of gigaohm seal formation during targeted patch clamp recording experiments while maintaining excellent neuronal preservation, thereby facilitating challenging experimental applications. Representative results are provided from multi-neuron patch clamp recording experiments to assay synaptic connectivity in neocortical brain slices prepared from young adult transgenic mice and mature adult human neurosurgical specimens. Furthermore, the optimized NMDG protective recovery method of brain slicing is compatible with both juvenile and adult animals, thus resolving a limitation of the original methodology. In summary, a single media formulation and brain slicing procedure can be implemented across various species and ages to achieve excellent viability and tissue preservation.
本方案是脑片制备的N-甲基-D-葡萄糖胺(NMDG)保护性恢复方法的实用指南。最近的大量研究证实了该方法在增强神经元保存和提高脑片整体活力方面的效用。早期采用者对该技术的应用,促进了使用各种实验应用,并涵盖广泛动物年龄、脑区和细胞类型的脑功能详细研究。文中概述了使用优化的NMDG人工脑脊液(aCSF)培养基配方和改进程序来实施保护性恢复脑片技术的步骤,以便可靠地获得用于膜片钳电生理学的健康脑片。采用这种更新的方法,在靶向膜片钳记录实验中,千兆欧封接形成的速度和可靠性有了显著提高,同时保持了优异的神经元保存,从而便于开展具有挑战性的实验应用。提供了来自多神经元膜片钳记录实验的代表性结果,以分析从年轻成年转基因小鼠和成熟成年人类神经外科标本制备的新皮质脑片中的突触连接性。此外,优化的NMDG脑片保护性恢复方法适用于幼年和成年动物,从而解决了原始方法的一个局限性。总之,单一的培养基配方和脑片制备程序可应用于各种物种和年龄,以实现优异的活力和组织保存。