Automated computation of nerve fibre inclinations from 3D polarised light imaging measurements of brain tissue

Journal Article (2022)
Author(s)

Miriam Menzel (Forschungszentrum Jülich)

Jan A. Reuter (Forschungszentrum Jülich)

David Gräßel (Forschungszentrum Jülich)

Irene Costantini (University of Florence, Istituto Nazionale di Ottica, Consiglio Nazionale delle Ricerche)

Katrin Amunts (Heinrich Heine University, Forschungszentrum Jülich)

Markus Axer (Forschungszentrum Jülich)

Affiliation
External organisation
DOI related publication
https://doi.org/10.1038/s41598-022-08140-0
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Publication Year
2022
Language
English
Affiliation
External organisation
Issue number
1
Volume number
12
Article number
4328
Downloads counter
172

Abstract

The method 3D polarised light imaging (3D-PLI) measures the birefringence of histological brain sections to determine the spatial course of nerve fibres (myelinated axons). While the in-plane fibre directions can be determined with high accuracy, the computation of the out-of-plane fibre inclinations is more challenging because they are derived from the amplitude of the birefringence signals, which depends e.g. on the amount of nerve fibres. One possibility to improve the accuracy is to consider the average transmitted light intensity (transmittance weighting). The current procedure requires effortful manual adjustment of parameters and anatomical knowledge. Here, we introduce an automated, optimised computation of the fibre inclinations, allowing for a much faster, reproducible determination of fibre orientations in 3D-PLI. Depending on the degree of myelination, the algorithm uses different models (transmittance-weighted, unweighted, or a linear combination), allowing to account for regionally specific behaviour. As the algorithm is parallelised and GPU optimised, it can be applied to large data sets. Moreover, it only uses images from standard 3D-PLI measurements without tilting, and can therefore be applied to existing data sets from previous measurements. The functionality is demonstrated on unstained coronal and sagittal histological sections of vervet monkey and rat brains.

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