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High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level

The precise annotation and accurate identification of neural structures are prerequisites for studying mammalian brain function. The orientation of neurons and neural circuits is usually determined by mapping brain images to coarse axial-sampling planar reference atlases. However, individual differe...

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Detalles Bibliográficos
Autores principales: Gong, Hui, Xu, Dongli, Yuan, Jing, Li, Xiangning, Guo, Congdi, Peng, Jie, Li, Yuxin, Schwarz, Lindsay A., Li, Anan, Hu, Bihe, Xiong, Benyi, Sun, Qingtao, Zhang, Yalun, Liu, Jiepeng, Zhong, Qiuyuan, Xu, Tonghui, Zeng, Shaoqun, Luo, Qingming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932192/
https://www.ncbi.nlm.nih.gov/pubmed/27374071
http://dx.doi.org/10.1038/ncomms12142
Descripción
Sumario:The precise annotation and accurate identification of neural structures are prerequisites for studying mammalian brain function. The orientation of neurons and neural circuits is usually determined by mapping brain images to coarse axial-sampling planar reference atlases. However, individual differences at the cellular level likely lead to position errors and an inability to orient neural projections at single-cell resolution. Here, we present a high-throughput precision imaging method that can acquire a co-localized brain-wide data set of both fluorescent-labelled neurons and counterstained cell bodies at a voxel size of 0.32 × 0.32 × 2.0 μm in 3 days for a single mouse brain. We acquire mouse whole-brain imaging data sets of multiple types of neurons and projections with anatomical annotation at single-neuron resolution. The results show that the simultaneous acquisition of labelled neural structures and cytoarchitecture reference in the same brain greatly facilitates precise tracing of long-range projections and accurate locating of nuclei.