Max Planck Institute for Biological Intelligence, Martinsried, Germany.
Max Planck Institute for Neurobiology of Behavior - caesar, Bonn, Germany.
Nat Methods. 2022 Nov;19(11):1357-1366. doi: 10.1038/s41592-022-01621-0. Epub 2022 Oct 24.
Dense reconstruction of synaptic connectivity requires high-resolution electron microscopy images of entire brains and tools to efficiently trace neuronal wires across the volume. To generate such a resource, we sectioned and imaged a larval zebrafish brain by serial block-face electron microscopy at a voxel size of 14 × 14 × 25 nm. We segmented the resulting dataset with the flood-filling network algorithm, automated the detection of chemical synapses and validated the results by comparisons to transmission electron microscopic images and light-microscopic reconstructions. Neurons and their connections are stored in the form of a queryable and expandable digital address book. We reconstructed a network of 208 neurons involved in visual motion processing, most of them located in the pretectum, which had been functionally characterized in the same specimen by two-photon calcium imaging. Moreover, we mapped all 407 presynaptic and postsynaptic partners of two superficial interneurons in the tectum. The resource developed here serves as a foundation for synaptic-resolution circuit analyses in the zebrafish nervous system.
突触连接的密集重建需要整个大脑的高分辨率电子显微镜图像和高效追踪神经元的工具。为了生成这样的资源,我们通过连续块面电子显微镜以 14×14×25nm 的体素大小对幼虫斑马鱼的大脑进行了切片和成像。我们使用填充网络算法对生成的数据集进行分割,自动检测化学突触,并通过与透射电子显微镜图像和明场显微镜重建的比较来验证结果。神经元及其连接以可查询和可扩展的数字通讯录的形式存储。我们重建了一个涉及视觉运动处理的 208 个神经元的网络,其中大多数位于顶盖中,在同一标本中,通过双光子钙成像对其进行了功能表征。此外,我们还绘制了 407 个前突触和两个顶盖中的浅层中间神经元的后突触伙伴。这里开发的资源是在斑马鱼神经系统中进行突触分辨率的电路分析的基础。