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Biophysical constraints of optogenetic inhibition at presynaptic terminals
We investigated the efficacy of optogenetic inhibition at presynaptic terminals using halorhodopsin, archaerhodopsin and chloride-conducting channelrhodopsins. Precisely timed activation of both archaerhodopsin and halorhodpsin at presynaptic terminals attenuated evoked release. However, sustained a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926958/ https://www.ncbi.nlm.nih.gov/pubmed/26950004 http://dx.doi.org/10.1038/nn.4266 |
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author | Mahn, Mathias Prigge, Matthias Ron, Shiri Levy, Rivka Yizhar, Ofer |
author_facet | Mahn, Mathias Prigge, Matthias Ron, Shiri Levy, Rivka Yizhar, Ofer |
author_sort | Mahn, Mathias |
collection | PubMed |
description | We investigated the efficacy of optogenetic inhibition at presynaptic terminals using halorhodopsin, archaerhodopsin and chloride-conducting channelrhodopsins. Precisely timed activation of both archaerhodopsin and halorhodpsin at presynaptic terminals attenuated evoked release. However, sustained archaerhodopsin activation was paradoxically associated with increased spontaneous release. Activation of chloride-conducting channelrhodopsins triggered neurotransmitter release upon light onset. Our results indicate that the biophysical properties of presynaptic terminals dictate unique boundary conditions for optogenetic manipulation. |
format | Online Article Text |
id | pubmed-4926958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-49269582016-09-22 Biophysical constraints of optogenetic inhibition at presynaptic terminals Mahn, Mathias Prigge, Matthias Ron, Shiri Levy, Rivka Yizhar, Ofer Nat Neurosci Article We investigated the efficacy of optogenetic inhibition at presynaptic terminals using halorhodopsin, archaerhodopsin and chloride-conducting channelrhodopsins. Precisely timed activation of both archaerhodopsin and halorhodpsin at presynaptic terminals attenuated evoked release. However, sustained archaerhodopsin activation was paradoxically associated with increased spontaneous release. Activation of chloride-conducting channelrhodopsins triggered neurotransmitter release upon light onset. Our results indicate that the biophysical properties of presynaptic terminals dictate unique boundary conditions for optogenetic manipulation. 2016-03-07 2016-04 /pmc/articles/PMC4926958/ /pubmed/26950004 http://dx.doi.org/10.1038/nn.4266 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Mahn, Mathias Prigge, Matthias Ron, Shiri Levy, Rivka Yizhar, Ofer Biophysical constraints of optogenetic inhibition at presynaptic terminals |
title | Biophysical constraints of optogenetic inhibition at presynaptic terminals |
title_full | Biophysical constraints of optogenetic inhibition at presynaptic terminals |
title_fullStr | Biophysical constraints of optogenetic inhibition at presynaptic terminals |
title_full_unstemmed | Biophysical constraints of optogenetic inhibition at presynaptic terminals |
title_short | Biophysical constraints of optogenetic inhibition at presynaptic terminals |
title_sort | biophysical constraints of optogenetic inhibition at presynaptic terminals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926958/ https://www.ncbi.nlm.nih.gov/pubmed/26950004 http://dx.doi.org/10.1038/nn.4266 |
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