Remote control of neuronal activity with a light-gated glutamate receptor

被引:242
作者
Szobota, Stephanie
Gorostiza, Pau
Del Bene, Filippo
Wyart, Claire
Fortin, Doris L.
Kolstad, Kathleen D.
Tulyathan, Orapim
Volgraf, Matthew
Numano, Rika
Aaron, Holly L.
Scott, Ethan K.
Kramer, Richard H.
Flannery, John
Baier, Herwig
Trauner, Dirk
Isacoff, Ehud Y. [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Biophys Grad Program, Berkeley, CA 94720 USA
[3] Univ Calif San Francisco, Dept Physiol, Program Neurosci, San Francisco, CA 94158 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
[5] Univ Calif Berkeley, Lawrence Berkeley Lab, Phys Biosci Div, Berkeley, CA 94720 USA
关键词
D O I
10.1016/j.neuron.2007.05.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The ability to stimulate select neurons in isolated tissue and in living animals is important for investigating their role in circuits and behavior. We show that the engineered light-gated ionotropic glutamate receptor (LiGluR), when introduced into neurons, enables remote control of their activity. Trains of action potentials are optimally evoked and extinguished by 380 nm and 500 nm light, respectively, while intermediate wavelengths provide graded control over the amplitude of depolarization. Light pulses of 1-5 ms in duration at similar to 380 nm trigger precisely timed action potentials and EPSP-like responses or can evoke sustained depolarizations that persist for minutes in the dark until extinguished by a short pulse of similar to 500 nm light. When introduced into sensory neurons in zebrafish larvae, activation of LiGluR reversibly blocks the escape response to touch. Our studies show that LiGluR provides robust control over neuronal activity, enabling the dissection and manipulation of neural circuitry in vivo.
引用
收藏
页码:535 / 545
页数:11
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