Transcranial optogenetic stimulation for functional mapping of the motor cortex

被引:86
|
作者
Hira, Riichiro [1 ,2 ,3 ]
Honkura, Naoki [1 ,2 ]
Noguchi, Jun [1 ,2 ]
Maruyama, Yoshio [3 ]
Augustine, George J. [4 ,5 ,6 ]
Kasai, Haruo [1 ,2 ]
Matsuzaki, Masanori [1 ,2 ,7 ]
机构
[1] Univ Tokyo, Lab Struct Physiol, Ctr Dis Biol & Integrat Med, Grad Sch Med,Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Ctr NanoBio Integrat, Tokyo 1130033, Japan
[3] Tohoku Univ, Sch Med, Dept Physiol, Sendai, Miyagi 980, Japan
[4] Duke Univ, Dept Neurobiol, Durham, NC USA
[5] Duke NUS Grad Med Sch, Program Neurosci & Behav Disorders, Lab Synapt Circuitry, Singapore 169547, Singapore
[6] ASTAR, Duke, NUS Neurosci Res Partnership, Singapore 138673, Singapore
[7] Japan Sci & Technol Agcy, PRESTO, Saitama, Japan
基金
美国国家卫生研究院;
关键词
Channelrhodopsin-2; Motor cortex; Mapping; Photostimulation; IN-VIVO; TRANSGENIC MICE; MICROSTIMULATION; RAT; CHANNELRHODOPSIN-2; ACTIVATION; PLASTICITY; NEURONS; CHANNEL;
D O I
10.1016/j.jneumeth.2009.02.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We developed a method that uses Channelrhodopsin-2 (ChR2) for transcranial optogenetic stimulation. This method is based on scanning a light beam over the brain, thereby photostimulating ChR2-expressing neurons in intact mice. As a proof of principle, we applied this technique to the motor cortex of transgenic mice expressing ChR2 in cortical pyramidal cells. Photostimulation induced limb movements that were time-locked with millisecond precision and could be induced at frequencies up to 20 Hz. By scanning this light beam, we could map the distribution of neurons associated with limb movement. With this approach we could simultaneously define motor maps controlling two limbs and could reproducibly generate such cortical motor maps over periods of weeks. This method allows non-invasive mapping of brain circuitry in living animals and could help define the connection between behavior and brain circuitry. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:258 / 263
页数:6
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