Random-access Two-photon Microscopy for Neural Activity Observation

被引:1
|
作者
Jiang Run-Hua [1 ]
Lu Xiao-Hua [1 ]
Li De-Rong [1 ]
Quan Ting-Wei [1 ]
Liu Xiu-Li [1 ]
Luo Qing-Ming [1 ]
Zeng Shao-Qun [1 ]
机构
[1] Huazhong Univ Sci & Technol, Britton Chance Ctr Biomed Photon, Wuhan Natl Lab Optoelect, Coll Life Sci & Technol, Wuhan 430074, Peoples R China
关键词
femtosecond laser; random-access scan; acousto-optic deflector; dispersion compensation; two-photon microscopy; calcium signal; spike reconstruction; LASER-SCANNING MICROSCOPY; ANGULAR-DISPERSION; TEMPORAL DISPERSION; FEMTOSECOND PULSES; NEURONAL-ACTIVITY; IN-VIVO; FLUORESCENCE MICROSCOPY; GAUSSIAN PULSES; HIGH-SPEED; COMPENSATION;
D O I
10.3724/SP.J.1206.2012.00234
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two-photon microscope has become an important instrument in neuroscience research. However, the current commercial instruments can hardly meet the need for the detection of neural signal in millisecond scale due to their low imaging rates. Fast random-access two-photon microscopy based on acousto-optic deflector (AOD) has the potential for increasing the observation speed while maintaining adequate signal to noise ratio (SNR). We summarize the latest related research progress. It is demonstrated from four parts, including the spatio-temporal evolution theory of the femtosecond laser after passing the angular dispersion devices, dispersion compensation method for AOD, random-access two-photon microscopy instrument, and calcium signal identification method in the instrument applications. In the end, the future development trends for random-access two-photon microscopy are discussed. The systematic and in-deep research on this technology will provide a new tool for the neural activity observation and boost the development of brain science.
引用
收藏
页码:505 / 512
页数:8
相关论文
共 41 条
  • [1] High-speed, random-access fluorescence microscopy .1. High-resolution optical recording with voltage-sensitive dyes and ion indicators
    Bullen, A
    Patel, SS
    Saggau, P
    [J]. BIOPHYSICAL JOURNAL, 1997, 73 (01) : 477 - 491
  • [2] 2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY
    DENK, W
    STRICKLER, JH
    WEBB, WW
    [J]. SCIENCE, 1990, 248 (4951) : 73 - 76
  • [3] Enhanced dispersion compensation capability of angular elements based on beam expansion
    Du, Rui
    Jiang, Runhua
    Fu, Ling
    [J]. OPTICS EXPRESS, 2009, 17 (19): : 16415 - 16422
  • [4] Nonlinear optical microscopy based on double-clad photonic crystal fibers
    Fu, L
    Gan, XS
    Gu, M
    [J]. OPTICS EXPRESS, 2005, 13 (14) : 5528 - 5534
  • [5] Double-clad photonic crystal fiber coupler for compact nonlinear optical microscopy imaging
    Fu, Ling
    Gu, Min
    [J]. OPTICS LETTERS, 2006, 31 (10) : 1471 - 1473
  • [6] In vivo calcium Imaging of neural network function
    Goebel, Werner
    Helmchen, Fritjof
    [J]. PHYSIOLOGY, 2007, 22 (06) : 358 - 365
  • [7] Population imaging of ongoing neuronal activity in the visual cortex of awake rats
    Greenberg, David S.
    Houweling, Arthur R.
    Kerr, Jason N. D.
    [J]. NATURE NEUROSCIENCE, 2008, 11 (07) : 749 - 751
  • [8] 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
  • [9] Optical probing of neuronal ensemble activity
    Grewe, Benjamin F.
    Helmchen, Fritjof
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 2009, 19 (05) : 520 - 529
  • [10] Deep tissue two-photon microscopy
    Helmchen, F
    Denk, W
    [J]. NATURE METHODS, 2005, 2 (12) : 932 - 940