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

被引:139
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
英国工程与自然科学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会;
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
    Botcherby, E. J.
    Juskaitis, R.
    Booth, M. J.
    Wilson, T.
    [J]. OPTICS COMMUNICATIONS, 2008, 281 (04) : 880 - 887
  • [3] Aberration-free optical refocusing in high numerical aperture microscopy
    Botcherby, Edward J.
    Juskaitis, Rimas
    Booth, Martin J.
    Wilson, Tony
    [J]. OPTICS LETTERS, 2007, 32 (14) : 2007 - 2009
  • [4] 2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY
    DENK, W
    STRICKLER, JH
    WEBB, WW
    [J]. SCIENCE, 1990, 248 (4951) : 73 - 76
  • [5] VISUALIZING UNSTAINED NEURONS IN LIVING BRAIN-SLICES BY INFRARED DIC-VIDEOMICROSCOPY
    DODT, HU
    ZIEGLGANSBERGER, W
    [J]. BRAIN RESEARCH, 1990, 537 (1-2) : 333 - 336
  • [6] Targeted bulk-loading of fluorescent indicators for two-photon brain imaging in vivo
    Garaschuk, Olga
    Milos, Ruxandra-Iulia
    Konnerth, Arthur
    [J]. NATURE PROTOCOLS, 2006, 1 (01) : 380 - 386
  • [7] New angles on neuronal dendrites in vivo
    Goebel, Werner
    Helmchen, Fritjof
    [J]. JOURNAL OF NEUROPHYSIOLOGY, 2007, 98 (06) : 3770 - 3779
  • [8] Imaging cellular network dynamics in three dimensions using fast 3D laser scanning
    Goebel, Werner
    Kampa, Bjoern M.
    Helmchen, Fritjof
    [J]. NATURE METHODS, 2007, 4 (01) : 73 - 79
  • [9] Fast two-layer two-photon imaging of neuronal cell populations using an electrically tunable lens
    Grewe, Benjamin F.
    Voigt, Fabian F.
    Van't Hoff, Marcel
    Helmchen, Fritjof
    [J]. BIOMEDICAL OPTICS EXPRESS, 2011, 2 (07): : 2035 - 2046
  • [10] High-speed in vivo calcium imaging reveals neuronal network activity with near-millisecond precision
    Grewe, Benjamin F.
    Langer, Dominik
    Kasper, Hansjoerg
    Kampa, Bjoern M.
    Helmchen, Fritjof
    [J]. NATURE METHODS, 2010, 7 (05) : 399 - U91