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 ( ) OCT with a high-resolution ( ) OCT to acquire whole mouse brains at low resolution and to target specific regions of interest (ROIs) at high reso...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurophotonics (Print) 2018-10, Vol.5 (4), p.045004-045004
Hauptverfasser: Lefebvre, Joël, Delafontaine-Martel, Patrick, Pouliot, Philippe, Girouard, Hélène, Descoteaux, Maxime, Lesage, Frédéric
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:An automated dual-resolution serial optical coherence tomography (2R-SOCT) scanner is developed. The serial histology system combines a low-resolution ( ) OCT with a high-resolution ( ) OCT to acquire whole mouse brains at low resolution and to target specific regions of interest (ROIs) at high resolution. The 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 mouse brains prior to automated histology. Using this imaging system, 3 whole mouse brains are imaged, and 250 high-resolution 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.
ISSN:2329-423X
2329-4248
DOI:10.1117/1.NPh.5.4.045004