Kilohertz frame-rate two-photon tomography

被引:113
作者
Kazemipour, Abbas [1 ,2 ]
Novak, Ondrej [1 ,3 ]
Flickinger, Daniel [1 ]
Marvin, Jonathan S. [1 ]
Abdelfattah, Ahmed S. [1 ]
King, Jonathan [4 ]
Borden, Philip M. [1 ]
Kim, Jeong Jun [1 ]
Al-Abdullatif, Sarah H. [5 ]
Deal, Parker E. [5 ]
Miller, Evan W. [5 ,6 ,7 ]
Schreiter, Eric R. [1 ]
Druckmann, Shaul [1 ,2 ]
Svoboda, Karel [1 ]
Looger, Loren L. [1 ]
Podgorski, Kaspar [1 ]
机构
[1] Howard Hughes Med Inst, Janelia Res Campus, Ashburn, VA 20147 USA
[2] Stanford Univ, Dept Neuroradiol, Stanford, CA 94305 USA
[3] Charles Univ Prague, Med Fac 2, Prague, Czech Republic
[4] Vidrio Technol, Ashburn, VA USA
[5] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[6] Univ Calif Berkeley, Dept Mol & Cell Biol, 229 Stanley Hall, Berkeley, CA 94720 USA
[7] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
FLUORESCENCE MICROSCOPY; CALCIUM TRANSIENTS; NMDA RECEPTORS; SINGLE SPINES; RESOLUTION; VOLTAGE; LIGHT; DECONVOLUTION; NEURONS; GLUTAMATE;
D O I
10.1038/s41592-019-0493-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Point-scanning two-photon microscopy enables high-resolution imaging within scattering specimens such as the mammalian brain, but sequential acquisition of voxels fundamentally limits its speed. We developed a two-photon imaging technique that scans lines of excitation across a focal plane at multiple angles and computationally recovers high-resolution images, attaining voxel rates of over 1 billion Hz in structured samples. Using a static image as a prior for recording neural activity, we imaged visually evoked and spontaneous glutamate release across hundreds of dendritic spines in mice at depths over 250 mu m and frame rates over 1 kHz. Dendritic glutamate transients in anesthetized mice are synchronized within spatially contiguous domains spanning tens of micrometers at frequencies ranging from 1-100 Hz. We demonstrate millisecond-resolved recordings of acetylcholine and voltage indicators, three-dimensional single-particle tracking and imaging in densely labeled cortex. Our method surpasses limits on the speed of raster-scanned imaging imposed by fluorescence lifetime.
引用
收藏
页码:778 / +
页数:13
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