Aberration-free three-dimensional multiphoton imaging of neuronal activity at kHz rates

被引:143
作者
Botcherby, Edward J. [1 ]
Smith, Christopher W. [1 ]
Kohl, Michael M. [2 ,3 ]
Debarre, Delphine [1 ,4 ]
Booth, Martin J. [1 ]
Juskaitis, Rimas [1 ]
Paulsen, Ole [2 ,3 ]
Wilson, Tony [1 ]
机构
[1] Univ Oxford, Dept Engn Sci, Oxford OX1 3PJ, England
[2] Univ Oxford, Dept Physiol Anat & Genet, Oxford OX1 3PT, England
[3] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3EG, England
[4] Ecole Polytech, Lab Opt & Biosci, F-91128 Palaiseau, France
基金
英国惠康基金; 英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
fluorescence microscopy; multiphoton imaging; multiphoton microscopy; three-dimensional microscopy; 2-PHOTON; MICROSCOPY; DYNAMICS;
D O I
10.1073/pnas.1111662109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multiphoton microscopy is a powerful tool in neuroscience, promising to deliver important data on the spatiotemporal activity within individual neurons as well as in networks of neurons. A major limitation of current technologies is the relatively slow scan rates along the z direction compared to the kHz rates obtainable in the x and y directions. Here, we describe a custom-built microscope system based on an architecture that allows kHz scan rates over hundreds of microns in all three dimensions without introducing aberration. We further demonstrate how this high-speed 3D multiphoton imaging system can be used to study neuronal activity at millisecond resolution at the subcellular as well as the population level.
引用
收藏
页码:2919 / 2924
页数:6
相关论文
共 23 条
[1]  
[Anonymous], 2000, Principles of optics: electromagnetic theory of propagation, interference and diffraction of light
[2]   An optical technique for remote focusing in microscopy [J].
Botcherby, E. J. ;
Juskaitis, R. ;
Booth, M. J. ;
Wilson, T. .
OPTICS COMMUNICATIONS, 2008, 281 (04) :880-887
[3]   Aberration-free optical refocusing in high numerical aperture microscopy [J].
Botcherby, Edward J. ;
Juskaitis, Rimas ;
Booth, Martin J. ;
Wilson, Tony .
OPTICS LETTERS, 2007, 32 (14) :2007-2009
[4]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[5]   VISUALIZING UNSTAINED NEURONS IN LIVING BRAIN-SLICES BY INFRARED DIC-VIDEOMICROSCOPY [J].
DODT, HU ;
ZIEGLGANSBERGER, W .
BRAIN RESEARCH, 1990, 537 (1-2) :333-336
[6]   Targeted bulk-loading of fluorescent indicators for two-photon brain imaging in vivo [J].
Garaschuk, Olga ;
Milos, Ruxandra-Iulia ;
Konnerth, Arthur .
NATURE PROTOCOLS, 2006, 1 (01) :380-386
[7]   New angles on neuronal dendrites in vivo [J].
Goebel, Werner ;
Helmchen, Fritjof .
JOURNAL OF NEUROPHYSIOLOGY, 2007, 98 (06) :3770-3779
[8]   Imaging cellular network dynamics in three dimensions using fast 3D laser scanning [J].
Goebel, Werner ;
Kampa, Bjoern M. ;
Helmchen, Fritjof .
NATURE METHODS, 2007, 4 (01) :73-79
[9]   Fast two-layer two-photon imaging of neuronal cell populations using an electrically tunable lens [J].
Grewe, Benjamin F. ;
Voigt, Fabian F. ;
Van't Hoff, Marcel ;
Helmchen, Fritjof .
BIOMEDICAL OPTICS EXPRESS, 2011, 2 (07) :2035-2046
[10]   High-speed in vivo calcium imaging reveals neuronal network activity with near-millisecond precision [J].
Grewe, Benjamin F. ;
Langer, Dominik ;
Kasper, Hansjoerg ;
Kampa, Bjoern M. ;
Helmchen, Fritjof .
NATURE METHODS, 2010, 7 (05) :399-U91