Optogenetic manipulation of neural activity in freely moving Caenorhabditis elegans

被引:97
|
作者
Leifer, Andrew M. [1 ,2 ]
Fang-Yen, Christopher [1 ,2 ,3 ]
Gershow, Marc [1 ,2 ]
Alkema, Mark J. [4 ]
Samuel, Aravinthan D. T. [1 ,2 ]
机构
[1] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
[2] Harvard Univ, Ctr Brain Sci, Cambridge, MA 02138 USA
[3] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
[4] Univ Massachusetts, Sch Med, Dept Neurobiol, Worcester, MA USA
基金
美国国家科学基金会;
关键词
OPTICAL INTERROGATION; CHANNELRHODOPSIN-2; LOCOMOTION; CIRCUIT; CELLS;
D O I
10.1038/NMETH.1554
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We present an optogenetic illumination system capable of real-time light delivery with high spatial resolution to specified targets in freely moving Caenorhabditis elegans. A tracking microscope records the motion of an unrestrained worm expressing channelrhodopsin-2 or halorhodopsin in specific cell types. Image processing software analyzes the worm's position in each video frame, rapidly estimates the locations of targeted cells and instructs a digital micromirror device to illuminate targeted cells with laser light of the appropriate wavelengths to stimulate or inhibit activity. Because each cell in an unrestrained worm is a rapidly moving target, our system operates at high speed (similar to 50 frames per second) to provide high spatial resolution (similar to 30 mu m). To test the accuracy, flexibility and utility of our system, we performed optogenetic analyses of the worm motor circuit, egg-laying circuit and mechanosensory circuits that have not been possible with previous methods.
引用
收藏
页码:147 / U71
页数:8
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