Lu Xiaotang, Wu Yuelong, Schalek Richard L, Meirovitch Yaron, Berger Daniel R, Lichtman Jeff W
Department of Molecular and Cellular Biology and The Center for Brain Science, Harvard University, Cambridge, Massachusetts, 02138, USA.
bioRxiv. 2023 Sep 27:2023.09.26.558265. doi: 10.1101/2023.09.26.558265.
Mapping the complete synaptic connectivity of a mammalian brain would be transformative, revealing the pathways underlying perception, behavior, and memory. Serial section electron microscopy, via membrane staining using osmium tetroxide, is ideal for visualizing cells and synaptic connections but, in whole brain samples, faces significant challenges related to chemical treatment and volume changes. These issues can adversely affect both the ultrastructural quality and macroscopic tissue integrity. By leveraging time-lapse X-ray imaging and brain proxies, we have developed a 12-step protocol, ODeCO, that effectively infiltrates osmium throughout an entire mouse brain while preserving ultrastructure without any cracks or fragmentation, a necessary prerequisite for constructing the first comprehensive mouse brain connectome.
绘制哺乳动物大脑的完整突触连接图谱将具有变革性意义,能揭示感知、行为和记忆背后的神经通路。通过使用四氧化锇进行膜染色的连续切片电子显微镜技术,非常适合用于观察细胞和突触连接,但在全脑样本中,面临着与化学处理和体积变化相关的重大挑战。这些问题会对超微结构质量和宏观组织完整性产生不利影响。通过利用延时X射线成像和脑替代物,我们开发了一种12步方案,即ODeCO,该方案能有效地将锇渗透到整个小鼠大脑中,同时保持超微结构完整无裂缝或破碎,这是构建首个全面的小鼠脑连接组的必要前提条件。