Ultra-compact fiber-optic two-photon microscope for functional fluorescence imaging in vivo

被引:224
作者
Engelbrecht, Christoph J. [1 ]
Johnston, Richard S. [2 ,3 ]
Seibel, Eric J. [2 ,3 ]
Helmchen, Fritjof [1 ]
机构
[1] Univ Zurich, Brain Res Inst, Dept Neurophysiol, CH-8057 Zurich, Switzerland
[2] Univ Washington, Dept Mech Engn, Seattle, WA 98195 USA
[3] Univ Washington, Human Photon Lab, Seattle, WA 98195 USA
关键词
D O I
10.1364/OE.16.005556
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We present a small, lightweight two-photon fiberscope and demonstrate its suitability for functional imaging in the intact brain. Our device consists of a hollow-core photonic crystal fiber for efficient delivery of near-IR femtosecond laser pulses, a spiral fiber-scanner for resonant beam steering, and a gradient-index lens system for fluorescence excitation, dichroic beam splitting, and signal collection. Fluorescence light is remotely detected using a standard photomultiplier tube. All optical components have 1 mm dimensions and the microscope's headpiece weighs only 0.6 grams. The instrument achieves micrometer resolution at frame rates of typically 25 Hz with a field-of-view of up to 200 microns. We demonstrate functional imaging of calcium signals in Purkinje cell dendrites in the cerebellum of anesthetized rats. The microscope will be easily portable by a rat or mouse and thus should enable functional imaging in freely behaving animals. (C) 2008 Optical Society of America.
引用
收藏
页码:5556 / 5564
页数:9
相关论文
共 38 条
[1]   Cortical calcium waves in resting newborn mice [J].
Adelsberger, H ;
Garaschuk, O ;
Konnerth, A .
NATURE NEUROSCIENCE, 2005, 8 (08) :988-990
[2]  
Cardoso J-F, BLIND SOURCE SEPARAT
[3]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[4]   Photon upmanship: Why multiphoton imaging is more than a gimmick [J].
Denk, W ;
Svoboda, K .
NEURON, 1997, 18 (03) :351-357
[5]   Imaging large-scale neural activity with cellular resolution in awake, mobile mice [J].
Dombeck, Daniel A. ;
Khabbaz, Anton N. ;
Collman, Forrest ;
Adelman, Thomas L. ;
Tank, David W. .
NEURON, 2007, 56 (01) :43-57
[6]   Resolution enhancement in a light-sheet-based microscope (SPIM) [J].
Engelbrecht, Christoph J. ;
Stelzer, Ernst H. K. .
OPTICS LETTERS, 2006, 31 (10) :1477-1479
[7]   Fiber-optic fluorescence imaging [J].
Flusberg, BA ;
Cocker, ED ;
Piyawattanametha, W ;
Jung, JC ;
Cheung, ELM ;
Schnitzer, MJ .
NATURE METHODS, 2005, 2 (12) :941-950
[8]   In vivo brain imaging using a portable 3.9 gram two-photon fluorescence microendoscope [J].
Flusberg, BA ;
Lung, JC ;
Cocker, ED ;
Anderson, EP ;
Schnitzer, MJ .
OPTICS LETTERS, 2005, 30 (17) :2272-2274
[9]   Fibre-optic nonlinear optical microscopy and endoscopy [J].
Fu, L. ;
Gu, M. .
JOURNAL OF MICROSCOPY, 2007, 226 (03) :195-206
[10]   Nonlinear optical endoscopy based on a double-clad photonic crystal fiber and a MEMS mirror [J].
Fu, L ;
Jain, A ;
Xie, HK ;
Cranfield, C ;
Gu, M .
OPTICS EXPRESS, 2006, 14 (03) :1027-1032