Multifocal fluorescence video-rate imaging of centimetre-wide arbitrarily shaped brain surfaces at micrometric resolution

被引:9
|
作者
Xie, Hao [1 ,2 ]
Han, Xiaofei [1 ,2 ]
Xiao, Guihua [3 ]
Xu, Hanyun [4 ]
Zhang, Yuanlong [1 ,2 ]
Zhang, Guoxun [1 ,2 ]
Li, Qingwei [5 ]
He, Jing [1 ,2 ]
Zhu, Dan [6 ]
Yu, Xinguang [4 ]
Dai, Qionghai [1 ,2 ,3 ,7 ]
机构
[1] Tsinghua Univ, Dept Automat, Beijing, Peoples R China
[2] Tsinghua Univ, Inst Brain & Cognit Sci, Beijing, Peoples R China
[3] Tsinghua Univ, Beijing Natl Res Ctr Informat Sci & Technol, Beijing, Peoples R China
[4] First Med Ctr Chinese PLA Gen Hosp, Dept Neurosurg, Beijing, Peoples R China
[5] Tsinghua Univ, Sch Med, Beijing, Peoples R China
[6] Huazhong Univ Sci & Technol, Britton Chance Ctr Biomed Photon, MoE Key Lab Biomed Photon, Wuhan Natl Lab Optoelect Adv Biomed Imaging Facil, Wuhan, Peoples R China
[7] Tsinghua Univ, IDG McGovern Inst Brain Res, Beijing, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
EXTENDED DEPTH; FIELD; MICROSCOPY; REVEALS; SIGNALS; NEURONS; INJURY; SPACE; PLANE; LIMIT;
D O I
10.1038/s41551-023-01155-6
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Fluorescence microscopy allows for the high-throughput imaging of cellular activity across brain areas in mammals. However, capturing rapid cellular dynamics across the curved cortical surface is challenging, owing to trade-offs in image resolution, speed, field of view and depth of field. Here we report a technique for wide-field fluorescence imaging that leverages selective illumination and the integration of focal areas at different depths via a spinning disc with varying thickness to enable video-rate imaging of previously reconstructed centimetre-scale arbitrarily shaped surfaces at micrometre-scale resolution and at a depth of field of millimetres. By implementing the technique in a microscope capable of acquiring images at 1.68 billion pixels per second and resolving 16.8 billion voxels per second, we recorded neural activities and the trajectories of neutrophils in real time on curved cortical surfaces in live mice. The technique can be integrated into many microscopes and macroscopes, in both reflective and fluorescence modes, for the study of multiscale cellular interactions on arbitrarily shaped surfaces. A wide-field fluorescence microscope leveraging a spinning disc and high-speed cameras enables the recording of neural activities and neutrophil trajectories at micrometric resolution on curved cortical surfaces in live mice.
引用
收藏
页码:740 / 753
页数:23
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