Tim Indersmitten, Tamara Berdyyeva, Leah Aluisio, Timothy Lovenberg, Pascal Bonaventure, Ryan M. Wyatt
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引用次数: 3
Abstract
Imaging neuronal activity in awake behaving mice with miniature fluorescence microscopes requires the implementation of a variety of procedures. Surgeries are performed to gain access to the cell population of interest and to implant microscope components. After a recovery period, mice are trained to exhibit a desired behavior. Finally, neuronal activity is imaged and synchronized with that behavior. To take full advantage of the technology, selection of the calcium indicator and experimental design must be carefully considered. In this article, we explain the procedures and considerations that are critical for obtaining high-quality calcium imaging data. As an example, we describe how to utilize miniature fluorescence microscopy to image hippocampal place cell activity during linear track running in Thy1.GCaMP6f transgenic mice. © 2018 by John Wiley & Sons, Inc.
利用微型荧光显微镜成像海马位置细胞集合功能。GCaMP6f转基因小鼠
用微型荧光显微镜成像清醒行为小鼠的神经元活动需要实施各种程序。手术是为了获得感兴趣的细胞群和植入显微镜组件。经过一段恢复期后,老鼠被训练表现出期望的行为。最后,神经元活动被成像,并与这种行为同步。为了充分发挥该技术的优势,必须认真考虑钙指示剂的选择和实验设计。在本文中,我们解释了获得高质量钙成像数据的关键程序和注意事项。作为一个例子,我们描述了如何利用微型荧光显微镜成像海马位置细胞活动在线性轨道运行在Thy1。GCaMP6f转基因小鼠。©2018 by John Wiley &儿子,Inc。
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