| Literature DB >> 26158018 |
M Caroline Müllenbroich1, Ludovico Silvestri2, Leonardo Onofri3, Irene Costantini4, Marcel Van't Hoff1, Leonardo Sacconi2, Giulio Iannello5, Francesco S Pavone6.
Abstract
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.Entities:
Keywords: data management; high-throughput imaging; light-sheet microscopy; selective plane illumination microscopy; software management; whole brain imaging
Year: 2015 PMID: 26158018 PMCID: PMC4484248 DOI: 10.1117/1.NPh.2.4.041404
Source DB: PubMed Journal: Neurophotonics ISSN: 2329-423X Impact factor: 3.593