Innovations in ex vivo Light Sheet Fluorescence Microscopy

被引:8
|
作者
Delgado-Rodriguez, Pablo [1 ]
Jordan Brooks, Claire [1 ]
Jose Vaquero, Juan [1 ,2 ]
Munoz-Barrutia, Arrate [1 ,2 ]
机构
[1] Univ Carlos III Madrid, Dept Bioingn & Ingn Aerosp, Madrid, Spain
[2] Inst Invest Sanitaria Gregorio Maranon, Madrid, Spain
关键词
Microscopy; Fluorescence; Architecture; Image analysis; Quantification; Multimodal; OPTICAL PROJECTION TOMOGRAPHY; ILLUMINATION MICROSCOPY; WHOLE-BRAIN; TISSUE; SCALE; ULTRAMICROSCOPY; RECONSTRUCTION; EXCITATION; REVEALS; DEEP;
D O I
10.1016/j.pbiomolbio.2021.07.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Light Sheet Fluorescence Microscopy (LSFM) has revolutionized how optical imaging of biological specimens can be performed as this technique allows to produce 3D fluorescence images of entire samples with a high spatiotemporal resolution. In this manuscript, we aim to provide readers with an overview of the field of LSFM on ex vivo samples. Recent advances in LSFM architectures have made the technique widely accessible and have improved its acquisition speed and resolution, among other features. These developments are strongly supported by quantitative analysis of the huge image volumes produced thanks to the boost in computational capacities, the advent of Deep Learning techniques, and by the combination of LSFM with other imaging modalities. Namely, LSFM allows for the characterization of biological structures, disease manifestations and drug effectivity studies. This information can ultimately serve to develop novel diagnostic procedures, treatments and even to model the organs physiology in healthy and pathological conditions. (c) 2021 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:37 / 51
页数:15
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