A visualization pipeline for in vivo two-photon volumetric astrocytic calcium imaging.

用于体内双光子体积星形胶质细胞钙成像的可视化流程

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作者:Sun Qian, Hu Yusi, Deng Saiyue, Xiong Yanyu, Huang Zhili
Astrocytes, the multi-functional glial cells with the most abundant population in the brain, integrate information across their territories to regulate neuronal synaptic and cerebrovascular activities. Astrocytic calcium (Ca (2+)) signaling is the major readout of cellular functional state of astrocytes. The conventional two-photon in vivo imaging usually focuses on a single horizontal focal plane to capture the astrocytic Ca (2+) signals, which leaves >80% spatial information undetected. To fully probe the Ca (2+) activity across the whole astrocytic territory, we developed a pipeline for imaging and visualizing volumetric astrocytic Ca (2+) time-lapse images. With the pipeline, we discovered a new signal distribution pattern from three-dimensional (3D) astrocytic Ca (2+) imaging data of mice under isoflurane anesthetic states. The tools developed in this study enable a better understanding of the spatiotemporal patterns of astrocytic activity in 3D space.

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