Millisecond-Timescale Optical Control of Neural Dynamics in the Nonhuman Primate Brain

被引:378
作者
Han, Xue [1 ]
Qian, Xiaofeng [1 ]
Bernstein, Jacob G. [1 ]
Zhou, Hui-hui [2 ]
Franzesi, Giovanni Talei [1 ]
Stern, Patrick [3 ]
Bronson, Roderick T. [3 ]
Graybiel, Ann M. [2 ]
Desimone, Robert [2 ]
Boyden, Edward S. [1 ,2 ,4 ]
机构
[1] MIT, Media Lab, Synthet Neurobiol Grp, Cambridge, MA 02139 USA
[2] MIT, McGovern Inst, Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
[3] MIT, Koch Ctr Canc Res, Cambridge, MA 02139 USA
[4] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
SENSORY-MOTOR CORTEX; MAMMALIAN NEURONS; VISUAL-CORTEX; GABA NEURONS; IN-VIVO; PROTEIN; CHANNELS; HYPERPOLARIZATION; MICROSTIMULATION; INHIBITION;
D O I
10.1016/j.neuron.2009.03.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To understand how brain states and behaviors are generated by neural circuits, it would be useful to be able to perturb precisely the activity of specific cell types and pathways in the nonhuman primate nervous system. We used lentivirus to target the light-activated cation channel channelrhodopsin-2 (ChR2) specifically to excitatory neurons of the macaque frontal cortex. Using a laser-coupled optical fiber in conjunction with a recording microelectrode, we showed that activation of excitatory neurons resulted in well-timed excitatory and suppressive influences on neocortical neural networks. ChR2 was safely expressed, and could mediate optical neuromodulation, in primate neocortex over many months. These findings highlight a methodology for investigating the causal role of specific cell types in nonhuman primate neural computation, cognition, and behavior, and open up the possibility of a new generation of ultraprecise neurological and psychiatric therapeutics via cell-type-specific optical neural control prosthetics.
引用
收藏
页码:191 / 198
页数:8
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