Micromirror structured illumination microscope for high-speed in vivo drosophila brain imaging

被引:9
作者
Masson, A. [1 ]
Pedrazzani, M. [1 ]
Benrezzak, S. [1 ]
Tchenio, P. [1 ,2 ]
Preat, T. [2 ]
Nutarelli, D. [1 ]
机构
[1] Univ Paris 11, CNRS, ENS Cachan, Lab Aime Cotton, F-91405 Orsay, France
[2] ESPCI, CNRS, Unite Neurobiol, F-75005 Paris, France
来源
OPTICS EXPRESS | 2014年 / 22卷 / 02期
关键词
TARGETED GENE-EXPRESSION; VOLTAGE-SENSITIVE DYES; MUSHROOM BODY; DYNAMICS; LIGHT;
D O I
10.1364/OE.22.001243
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Genetic tools and especially genetically encoded fluorescent reporters have given a special place to optical microscopy in drosophila neurobiology research. In order to monitor neural networks activity, high speed and sensitive techniques, with high spatial resolution are required. Structured illumination microscopies are wide-field approaches with optical sectioning ability. Despite the large progress made with the introduction of the HiLo principle, they did not meet the criteria of speed and/or spatial resolution for drosophila brain imaging. We report on a new implementation that took advantage of micromirror matrix technology to structure the illumination. Thus, we showed that the developed instrument exhibits a spatial resolution close to that of confocal microscopy but it can record physiological responses with a speed improved by more than an order a magnitude. (C) 2014 Optical Society of America
引用
收藏
页码:1243 / 1256
页数:14
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