Recording Neural Activity in Unrestrained Animals with Three-Dimensional Tracking Two-Photon Microscopy

被引:28
作者
Karagyozov, Doycho [1 ]
Skanata, Mirna Mihovilovic [1 ]
Lesar, Amanda [1 ]
Gershow, Marc [1 ,2 ,3 ]
机构
[1] NYU, Dept Phys, 4 Washington Pl, New York, NY 10003 USA
[2] NYU, Ctr Neural Sci, New York, NY 10003 USA
[3] NYU, Inst Neurosci, New York, NY 10003 USA
来源
CELL REPORTS | 2018年 / 25卷 / 05期
基金
美国国家科学基金会;
关键词
SINGLE-PARTICLE TRACKING; CELLULAR RESOLUTION; DROSOPHILA; CHEMOTAXIS; DYNAMICS; RESOURCE; CIRCUIT; CELLS; GAL4;
D O I
10.1016/j.celrep.2018.10.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Optical recordings of neural activity in behaving animals can reveal the neural correlates of decision making, but brain motion, which often accompanies behavior, compromises these measurements. Two-photon point-scanning microscopy is especially sensitive to motion artifacts, and two-photon recording of activity has required rigid coupling between the brain and microscope. We developed a two-photon tracking microscope with extremely low-latency (360 ms) feedback implemented in hardware. This microscope can maintain continuous focus on neurons moving with velocities of 3 mm/s and accelerations of 1 m/s(2) both in-plane and axially. We recorded calcium dynamics of motor neurons and inter-neurons in unrestrained freely behaving fruit fly larvae, correlating neural activity with stimulus presentations and behavioral outputs, and we measured light-induced depolarization of a visual interneuron in a moving animal using a genetically encoded voltage indicator. Our technique can be extended to stabilize recordings in a variety of moving substrates.
引用
收藏
页码:1371 / +
页数:23
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