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Deep Learning to Decipher the Progression and Morphology of Axonal Degeneration.

Authors :
Palumbo, Alex
Grüning, Philipp
Landt, Svenja Kim
Heckmann, Lara Eleen
Bartram, Luisa
Pabst, Alessa
Flory, Charlotte
Ikhsan, Maulana
Pietsch, Sören
Schulz, Reinhard
Kren, Christopher
Koop, Norbert
Boltze, Johannes
Madany Mamlouk, Amir
Zille, Marietta
Source :
Cells (2073-4409). Oct2021, Vol. 10 Issue 10, p2539-2539. 1p.
Publication Year :
2021

Abstract

Axonal degeneration (AxD) is a pathological hallmark of many neurodegenerative diseases. Deciphering the morphological patterns of AxD will help to understand the underlying mechanisms and develop effective therapies. Here, we evaluated the progression of AxD in cortical neurons using a novel microfluidic device together with a deep learning tool that we developed for the enhanced-throughput analysis of AxD on microscopic images. The trained convolutional neural network (CNN) sensitively and specifically segmented the features of AxD including axons, axonal swellings, and axonal fragments. Its performance exceeded that of the human evaluators. In an in vitro model of AxD in hemorrhagic stroke induced by the hemolysis product hemin, we detected a time-dependent degeneration of axons leading to a decrease in axon area, while axonal swelling and fragment areas increased. Axonal swellings preceded axon fragmentation, suggesting that swellings may be reliable predictors of AxD. Using a recurrent neural network (RNN), we identified four morphological patterns of AxD (granular, retraction, swelling, and transport degeneration). These findings indicate a morphological heterogeneity of AxD in hemorrhagic stroke. Our EntireAxon platform enables the systematic analysis of axons and AxD in time-lapse microscopy and unravels a so-far unknown intricacy in which AxD can occur in a disease context. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20734409
Volume :
10
Issue :
10
Database :
Academic Search Index
Journal :
Cells (2073-4409)
Publication Type :
Academic Journal
Accession number :
153249678
Full Text :
https://doi.org/10.3390/cells10102539