Comprehensive optical and data management infrastructure for high-throughput light-sheet microscopy of whole mouse brains

被引:16
|
作者
Muellenbroich, M. Caroline [1 ,2 ]
Silvestri, Ludovico [1 ,3 ]
Onofri, Leonardo [1 ,4 ]
Costantini, Irene [1 ]
van't Hoff, Marcel [1 ,2 ]
Sacconi, Leonardo [1 ,3 ]
Iannello, Giulio [4 ]
Pavone, Francesco S. [1 ,2 ,3 ,5 ]
机构
[1] Univ Florence, European Lab Nonlinear Spect, Via Nello Carrara 1, I-50019 Sesto Fiorentino, Italy
[2] Univ Florence, Dept Phys & Astron, I-50019 Sesto Fiorentino, Italy
[3] CNR, Natl Inst Opt, I-50019 Sesto Fiorentino, Italy
[4] Univ Campus Biomed Rome, I-00128 Rome, Italy
[5] Int Ctr Computat Neurophoton, I-50019 Sesto Fiorentino, Italy
关键词
light-sheet microscopy; selective plane illumination microscopy; whole brain imaging; data management; software management; high-throughput imaging; PLANE ILLUMINATION MICROSCOPY; INDUCED ABERRATIONS; SCALE; RESOLUTION; SYSTEMS; IMAGES; CELLS;
D O I
10.1117/1.NPh.2.4.041404
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Comprehensive mapping and quantification of neuronal projections in the central nervous system requires high-throughput imaging of large volumes with microscopic resolution. To this end, we have developed a confocal light-sheet microscope that has been optimized for three-dimensional (3-D) imaging of structurally intact clarified whole-mount mouse brains. We describe the optical and electromechanical arrangement of the microscope and give details on the organization of the microscope management software. The software orchestrates all components of the microscope, coordinates critical timing and synchronization, and has been written in a versatile and modular structure using the LabVIEW language. It can easily be adapted and integrated to other microscope systems and has been made freely available to the light-sheet community. The tremendous amount of data routinely generated by light-sheet microscopy further requires novel strategies for data handling and storage. To complete the full imaging pipeline of our high-throughput microscope, we further elaborate on big data management from streaming of raw images up to stitching of 3-D datasets. The mesoscale neuroanatomy imaged at micron-scale resolution in those datasets allows characterization and quantification of neuronal projections in unsectioned mouse brains. (C) The Authors.
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收藏
页数:13
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