Kim Tony Hyun, Zhang Yanping, Lecoq Jérôme, Jung Juergen C, Li Jane, Zeng Hongkui, Niell Cristopher M, Schnitzer Mark J
James H. Clark Center for Biomedical Engineering and Sciences, Stanford University, Stanford, CA 94305, USA; CNC Program, Stanford University, Stanford, CA 94305, USA.
James H. Clark Center for Biomedical Engineering and Sciences, Stanford University, Stanford, CA 94305, USA; CNC Program, Stanford University, Stanford, CA 94305, USA; Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.
Cell Rep. 2016 Dec 20;17(12):3385-3394. doi: 10.1016/j.celrep.2016.12.004.
A major technological goal in neuroscience is to enable the interrogation of individual cells across the live brain. By creating a curved glass replacement to the dorsal cranium and surgical methods for its installation, we developed a chronic mouse preparation providing optical access to an estimated 800,000-1,100,000 individual neurons across the dorsal surface of neocortex. Post-surgical histological studies revealed comparable glial activation as in control mice. In behaving mice expressing a Ca indicator in cortical pyramidal neurons, we performed Ca imaging across neocortex using an epi-fluorescence macroscope and estimated that 25,000-50,000 individual neurons were accessible per mouse across multiple focal planes. Two-photon microscopy revealed dendritic morphologies throughout neocortex, allowed time-lapse imaging of individual cells, and yielded estimates of >1 million accessible neurons per mouse by serial tiling. This approach supports a variety of optical techniques and enables studies of cells across >30 neocortical areas in behaving mice.
神经科学的一个主要技术目标是能够在活体大脑中对单个细胞进行检测。通过制作一个用于替换颅骨背侧的弧形玻璃以及安装它的手术方法,我们开发了一种慢性小鼠制备方法,可通过光学手段观察新皮层背表面估计80万至110万个单个神经元。术后组织学研究显示,胶质细胞激活情况与对照小鼠相当。在皮层锥体神经元中表达钙指示剂的行为小鼠中,我们使用落射荧光宏观显微镜对整个新皮层进行钙成像,估计每只小鼠在多个焦平面上可观察到25,000至50,000个单个神经元。双光子显微镜揭示了整个新皮层的树突形态,允许对单个细胞进行延时成像,并通过连续平铺估计每只小鼠可观察到超过100万个可及神经元。这种方法支持多种光学技术,并能够在行为小鼠中对超过30个新皮层区域的细胞进行研究。