Y. Choe, D. Mayerich, Jaerock Kwon, Daniel E. Miller, Ji Ryang Chung, C. Sung, J. Keyser, L. Abbott
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引用次数: 14
摘要
在本文中,我们将回顾一种新的显微镜模式,称为刀口扫描显微镜(KESM),我们已经发展了12年(自1999年以来),并讨论其与连接组学和神经网络研究的相关性。KESM的工作原理是同时对嵌入在硬聚合物树脂中的小动物大脑进行切片和成像,以便在约1 cm3的组织体积上实现接近各向同性的亚微米体素尺寸(0.6 μ m × 0.7 μ m × 1.0 μ m),足以容纳整个小鼠大脑。在这个分辨率下,可以看到树突、树突棘和轴突等形态学细节(对于像高尔基体这样的稀疏斑点)。KESM已成功用于扫描用高尔基体(神经元形态学)、尼氏体(体细胞)和印度墨水(脉管系统)染色的整个小鼠大脑,为小鼠大脑内微结构的系统级结构布局提供了前所未有的见解。在本文中,我们将展示来自KESM的全脑规模数据集,并讨论这些详细的系统级数据给连接组学和神经网络研究带来的挑战和机遇。
Knife-edge scanning microscopy for connectomics research
In this paper, we will review a novel microscopy modality called Knife-Edge Scanning Microscopy (KESM) that we have developed over the past twelve years (since 1999) and discuss its relevance to connectomics and neural networks research. The operational principle of KESM is to simultaneously section and image small animal brains embedded in hard polymer resin so that a near-isotropic, sub-micrometer voxel size of 0.6 µm × 0.7 µm × 1.0 µm can be achieved over ∼1 cm3 volume of tissue which is enough to hold an entire mouse brain. At this resolution, morphological details such as dendrites, dendritic spines, and axons are visible (for sparse stains like Golgi). KESM has been successfully used to scan whole mouse brains stained in Golgi (neuronal morphology), Nissl (somata), and India ink (vasculature), providing unprecedented insights into the system-level architectural layout of microstructures within the mouse brain. In this paper, we will present whole-brain-scale data sets from KESM and discuss challenges and opportunities posed to connectomics and neural networks research by such detailed yet system-level data.