Successful 3D imaging of cleared biological samples with light sheet fluorescence microscopy

被引:4
作者
Delage, Elise [1 ,2 ]
Guilbert, Thomas [3 ]
Yates, Frank [1 ,2 ]
机构
[1] SupBiotech, CellTechs Lab, Villejuif, France
[2] Univ Paris Saclay, Inst Francois Jacob Commissariatal Energie Atom& E, Serv Etud Pr & Infect Atyp, Fontenay Aux Roses, France
[3] Univ Paris, Inst Cochin, Inst Natl Sante & Rech Med U1016, Ctr Natl Rech Sci UMR 8104,UMR S1016, Paris, France
关键词
SINGLE-CELL RESOLUTION; ILLUMINATION MICROSCOPY; EXCITATION; GUIDE; DIMENSIONS;
D O I
10.1083/jcb.202307143
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In parallel with the development of tissue-clearing methods, over the last decade, light sheet fluorescence microscopy has contributed to major advances in various fields, such as cell and developmental biology and neuroscience. While biologists are increasingly integrating three-dimensional imaging into their research projects, their experience with the technique is not always up to their expectations. In response to a survey of specific challenges associated with sample clearing and labeling, image acquisition, and data analysis, we have critically assessed the recent literature to characterize the difficulties inherent to light sheet fluorescence microscopy applied to cleared biological samples and to propose solutions to overcome them. This review aims to provide biologists interested in light sheet fluorescence microscopy with a primer for the development of their imaging pipeline, from sample preparation to image analysis. Importantly, we believe that issues could be avoided with better anticipation of image analysis requirements, which should be kept in mind while optimizing sample preparation and acquisition parameters.
引用
收藏
页数:11
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