A calibrated optogenetic toolbox of stable zebrafish opsin lines

被引:39
作者
Antinucci, Paride [1 ]
Dumitrescu, Adna [2 ]
Deleuze, Charlotte [2 ]
Morley, Holly J. [1 ]
Leung, Kristie [1 ]
Hagley, Tom [1 ]
Kubo, Fumi [3 ,4 ]
Baier, Herwig [4 ]
Bianco, Isaac H. [1 ]
Wyart, Claire [2 ]
机构
[1] UCL, Dept Neurosci Physiol & Pharmacol, London, England
[2] Sorbonne Univ, Inst Cerveau & Moelle Epiniere ICM, Hop Pitie Salpetriere, CNRS,UPMC Univ Paris 06,INSERM, Paris, France
[3] Natl Insitute Genet, Ctr Frontier Res, Mishima, Shizuoka, Japan
[4] Max Planck Inst Neurobiol, Dept Genes Circuits Behav, Martinsried, Germany
基金
欧盟地平线“2020”; 英国惠康基金;
关键词
TARGETED GENE-EXPRESSION; CIRCUIT FUNCTION; OPTICAL CONTROL; IN-VIVO; NEURONS; TRANSPOSON; BEHAVIOR; DISSECTION; CHANNELRHODOPSINS; TRANSGENESIS;
D O I
10.7554/eLife.54937
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Optogenetic actuators with diverse spectral tuning, ion selectivity and kinetics are constantly being engineered providing powerful tools for controlling neural activity with subcellular resolution and millisecond precision. Achieving reliable and interpretable in vivo optogenetic manipulations requires reproducible actuator expression and calibration of photocurrents in target neurons. Here, we developed nine transgenic zebrafish lines for stable opsin expression and calibrated their efficacy in vivo. We first used high-throughput behavioural assays to compare opsin ability to elicit or silence neural activity. Next, we performed in vivo whole-cell electrophysiological recordings to quantify the amplitude and kinetics of photocurrents and test opsin ability to precisely control spiking. We observed substantial variation in efficacy, associated with differences in both opsin expression level and photocurrent characteristics, and identified conditions for optimal use of the most efficient opsins. Overall, our calibrated optogenetic toolkit will facilitate the design of controlled optogenetic circuit manipulations.
引用
收藏
页数:31
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