Ide Saya, Kajiwara Motoki, Imai Hirohiko, Shimono Masanori
Graduate School of Medicine and Faculty of Medicine, Kyoto University.
Graduate School of Informatics, Kyoto University.
J Vis Exp. 2019 May 12(147). doi: 10.3791/58911.
The human brain, being a multiscale system, has both macroscopic electrical signals, globally flowing along thick white-matter fiber bundles, and microscopic neuronal spikes, propagating along axons and dendrites. Both scales complement different aspects of human cognitive and behavioral functions. At the macroscopic level, MRI has been the current standard imaging technology, in which the smallest spatial resolution, voxel size, is 0.1-1 mm. Also, at the microscopic level, previous physiological studies were aware of nonuniform neuronal architectures within such voxels. This study develops a powerful way to accurately embed microscopic data into a macroscopic map by interfacing biological scientific research with technological advancements in 3D scanning technology. Since 3D scanning technology has mostly been used for engineering and industrial design until now, it is repurposed for the first time to embed microconnectomes into the whole brain while preserving natural spiking in living brain cells. In order to achieve this purpose, first, we constructed a scanning protocol to obtain accurate 3D images from living bio-organisms inherently challenging to image due to moist and reflective surfaces. Second, we trained to keep speed to prevent the degradation of living brain tissue, which is a key factor in retaining better conditions and recording more natural neuronal spikes from active neurons in the brain tissue. Two cortical surface images, independently extracted from two different imaging modules, namely MRI and 3D scanner surface images, surprisingly show a distance error of only 50 μm as mode value of the histogram. This accuracy is comparable in scale to the microscopic resolution of intercellular distances; also, it is stable among different individual mice. This new protocol, the 3D novel embedding overlapping (3D-NEO) protocol, bridges macroscopic and microscopic levels derived by this integrative protocol and accelerates new scientific findings to study comprehensive connectivity architectures (i.e., microconnectome).
人类大脑作为一个多尺度系统,既具有沿粗大的白质纤维束全局流动的宏观电信号,也具有沿轴突和树突传播的微观神经元尖峰。这两个尺度相辅相成,共同构成人类认知和行为功能的不同方面。在宏观层面,磁共振成像(MRI)一直是当前的标准成像技术,其最小空间分辨率即体素大小为0.1 - 1毫米。此外,在微观层面,先前的生理学研究已经意识到在这样的体素内神经元结构是不均匀的。本研究通过将生物科学研究与3D扫描技术的技术进步相结合,开发出一种强大的方法,能够将微观数据准确地嵌入宏观图谱中。由于到目前为止3D扫描技术大多用于工程和工业设计,所以首次将其重新用于在保留活脑细胞自然尖峰的同时将微观连接组嵌入整个大脑。为了实现这一目标,首先,我们构建了一个扫描协议,以从具有潮湿和反射表面、本身对成像具有挑战性的活生物体内获取准确的3D图像。其次,我们训练保持速度以防止活脑组织退化,这是保持更好条件并从脑组织中的活跃神经元记录更多自然神经元尖峰的关键因素。从两个不同的成像模块(即MRI和3D扫描仪表面图像)独立提取的两个皮质表面图像,令人惊讶地显示,直方图的众数距离误差仅为50微米。这个精度在尺度上与细胞间距离的微观分辨率相当;而且,在不同的个体小鼠之间也很稳定。这种新协议,即3D新型嵌入重叠(3D - NEO)协议,通过这种整合协议弥合了宏观和微观层面,并加速了对综合连接架构(即微观连接组)的新科学发现。