Optical control of neuronal excitation and inhibition using a single opsin protein, ChR2

The effect of electrical stimulation on neuronal membrane potential is frequency dependent. Low frequency electrical stimulation can evoke action potentials, whereas high frequency stimulation can inhibit action potential transmission. Optical stimulation of channelrhodopsin-2 (ChR2) expressed in ne...

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Bibliographic Details
Main Authors: Liske, Holly (Author), Qian, Xiang (Author), Deisseroth, Karl (Author), Delp, Scott (Author), Anikeeva, Polina Olegovna (Contributor)
Other Authors: Massachusetts Institute of Technology. Department of Materials Science and Engineering (Contributor)
Format: Article
Language:English
Published: Nature Publishing Group, 2014-02-19T17:40:29Z.
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Online Access:Get fulltext
LEADER 01857 am a22002293u 4500
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042 |a dc 
100 1 0 |a Liske, Holly  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Materials Science and Engineering  |e contributor 
100 1 0 |a Anikeeva, Polina Olegovna  |e contributor 
700 1 0 |a Qian, Xiang  |e author 
700 1 0 |a Deisseroth, Karl  |e author 
700 1 0 |a Delp, Scott  |e author 
700 1 0 |a Anikeeva, Polina Olegovna  |e author 
245 0 0 |a Optical control of neuronal excitation and inhibition using a single opsin protein, ChR2 
260 |b Nature Publishing Group,   |c 2014-02-19T17:40:29Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/85011 
520 |a The effect of electrical stimulation on neuronal membrane potential is frequency dependent. Low frequency electrical stimulation can evoke action potentials, whereas high frequency stimulation can inhibit action potential transmission. Optical stimulation of channelrhodopsin-2 (ChR2) expressed in neuronal membranes can also excite action potentials. However, it is unknown whether optical stimulation of ChR2-expressing neurons produces a transition from excitation to inhibition with increasing light pulse frequencies. Here we report optical inhibition of motor neuron and muscle activity in vivo in the cooled sciatic nerves of Thy1-ChR2-EYFP mice. We also demonstrate all-optical single-wavelength control of neuronal excitation and inhibition without co-expression of inhibitory and excitatory opsins. This all-optical system is free from stimulation-induced electrical artifacts and thus provides a new approach to investigate mechanisms of high frequency inhibition in neuronal circuits in vivo and in vitro. 
520 |a National Institutes of Health (U.S.) (Grant RO1NS080954) 
546 |a en_US 
655 7 |a Article 
773 |t Scientific Reports