High-speed two-photon microscopy with adaptive line-excitation

被引:0
|
作者
Li, Yunyang [1 ]
Guo, Shu [1 ]
Mattison, Ben [2 ,3 ]
Hu, Junjie [1 ]
Man, Kwun Nok Mimi [4 ,5 ]
Yang, Weijian [1 ,3 ]
机构
[1] Univ Calif Davis, Dept Elect & Comp Engn, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Biomed Engn, Davis, CA 95616 USA
[3] Univ Calif Davis, Biomed Engn Grad Grp, Davis, CA 95616 USA
[4] Univ Calif Davis, Dept Biochem & Mol Med, Davis, CA 95616 USA
[5] Max Planck Florida Inst Neurosci, Jupiter, FL 33458 USA
来源
OPTICA | 2024年 / 11卷 / 08期
基金
美国国家科学基金会;
关键词
MULTIPHOTON MICROSCOPY; CALCIUM;
D O I
10.1364/OPTICA.529930
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We present a two-photon fluorescence microscope designed for high-speed imaging of neural activity at cellular resolution. Our microscope uses an adaptive sampling scheme with line illumination. Instead of building images pixel by pixel via scanning a diffraction-limited spot across the sample, our scheme only illuminates the regions of interest (i.e., neuronal cell bodies) and samples a large area of them in a single measurement. Such a scheme significantly increases the imaging speed and reduces the overall laser power on the brain tissue. Using this approach, we performed high-speed imaging of the neuronal activity in mouse cortex in vivo. Our method provides a sampling strategy in laser-scanning two-photon microscopy and will be powerful for high-throughput imaging of neural activity.
引用
收藏
页码:1138 / 1145
页数:8
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