Abstract
AbstractWe report on an Adaptive Optics (AO) Light-Sheet Fluorescence Microscope compatible with neuroimaging, based on direct wavefront sensing without the requirement of a guide star. We demonstrate fast AO correction, typically within 500ms, of in-depth aberrations of the live adultDrosophilabrain, enabling to double the contrast when imaging with structural or calcium sensors. We quantify the gain in terms of image quality on multiply neuronal structures part of the sleep network in theDrosophilabrain, at various depths, and discuss the optimization of key parameters driving AO such as the number of corrected modes and the photon budget. We present a first design of a compact AO add-on that is compatible with integration into most of reported Light-Sheet setups and neuroimaging.
Publisher
Cold Spring Harbor Laboratory
Reference39 articles.
1. Whole-brain functional imaging at cellular resolution using light-sheet microscopy;Nature Methods,2013
2. Thomas Panier , Sebastián A. Romano , Raphaël Olive , Thomas Pietri , Germán Sumbre , Raphaël Candelier , and Georges Debrégeas . Fast functional imaging of multiple brain regions in intact zebrafish larvae using Selective Plane Illumination Microscopy. Frontiers in Neural Circuits, 7, 2013.
3. Greenspan. Fast near-whole–brain imaging in adult Drosophila during responses to stimuli and behavior;PLOS Biology,2019
4. In vivo large-scale analysis of Drosophila neuronal calcium traces by automated tracking of single somata;Scientific Reports,2020
5. Optical Sectioning Deep Inside Live Embryos by Selective Plane Illumination Microscopy;Science,2004
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献