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Fully automated dual-resolution serial optical coherence tomography aimed at diffusion MRI validation in whole mouse brains
An automated dual-resolution serial optical coherence tomography (2R-SOCT) scanner is developed. The serial histology system combines a low-resolution ([Formula: see text]) [Formula: see text] OCT with a high-resolution ([Formula: see text]) [Formula: see text] OCT to acquire whole mouse brains at l...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215086/ https://www.ncbi.nlm.nih.gov/pubmed/30681668 http://dx.doi.org/10.1117/1.NPh.5.4.045004 |
Sumario: | An automated dual-resolution serial optical coherence tomography (2R-SOCT) scanner is developed. The serial histology system combines a low-resolution ([Formula: see text]) [Formula: see text] OCT with a high-resolution ([Formula: see text]) [Formula: see text] OCT to acquire whole mouse brains at low resolution and to target specific regions of interest (ROIs) at high resolution. The [Formula: see text] ROIs positions are selected either manually by the microscope operator or using an automated ROI positioning selection algorithm. Additionally, a multimodal and multiresolution registration pipeline is developed in order to align the 2R-SOCT data onto diffusion MRI (dMRI) data acquired in the same ex vivo mouse brains prior to automated histology. Using this imaging system, 3 whole mouse brains are imaged, and 250 high-resolution [Formula: see text] three-dimensional ROIs are acquired. The capability of this system to perform multimodal imaging studies is demonstrated by labeling the ROIs using a mouse brain atlas and by categorizing the ROIs based on their associated dMRI measures. This reveals a good correspondence of the tissue microstructure imaged by the high-resolution OCT with various dMRI measures such as fractional anisotropy, number of fiber orientations, apparent fiber density, orientation dispersion, and intracellular volume fraction. |
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