Laboratory for Optics and Biosciences, Ecole polytechnique, CNRS, INSERM, IP Paris, Palaiseau, 91128, France.
Sorbonne Université, INSERM, CNRS, Institut de la Vision, 17 rue Moreau, Paris, 75012, France.
Nat Commun. 2019 Apr 10;10(1):1662. doi: 10.1038/s41467-019-09552-9.
Large-scale microscopy approaches are transforming brain imaging, but currently lack efficient multicolor contrast modalities. We introduce chromatic multiphoton serial (ChroMS) microscopy, a method integrating one-shot multicolor multiphoton excitation through wavelength mixing and serial block-face image acquisition. This approach provides organ-scale micrometric imaging of spectrally distinct fluorescent proteins and label-free nonlinear signals with constant micrometer-scale resolution and sub-micron channel registration over the entire imaged volume. We demonstrate tridimensional (3D) multicolor imaging over several cubic millimeters as well as brain-wide serial 2D multichannel imaging. We illustrate the strengths of this method through color-based 3D analysis of astrocyte morphology and contacts in the mouse cerebral cortex, tracing of individual pyramidal neurons within densely Brainbow-labeled tissue, and multiplexed whole-brain mapping of axonal projections labeled with spectrally distinct tracers. ChroMS will be an asset for multiscale and system-level studies in neuroscience and beyond.
大规模显微镜方法正在改变脑成像,但目前缺乏高效的多色对比模式。我们引入了色相差分双光子序列(ChroMS)显微镜,这是一种通过波长混合和串行块面图像采集实现单次多色双光子激发的方法。该方法可提供具有恒定微米级分辨率的器官尺度微尺度成像,以及整个成像体积中具有亚微米通道注册的光谱上不同的荧光蛋白和无标记非线性信号。我们展示了几立方毫米的三维(3D)多色成像以及全脑范围的二维多通道串行成像。我们通过基于颜色的 3D 分析来展示这种方法的优势,分析了小鼠大脑皮层中的星形胶质细胞形态和接触,在密集的 Brainbow 标记组织中追踪单个锥体神经元,以及用光谱上不同的示踪剂标记的轴突投射的多路复用全脑映射。ChroMS 将成为神经科学及其他领域的多尺度和系统级研究的有力工具。