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

Journal: Cells
Published Date:

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.

Authors

  • Alex Palumbo
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
  • Philipp Grüning
    Institute for Neuro- and Bioinformatics, University of Lübeck, 23562 Lübeck, Germany.
  • Svenja Kim Landt
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
  • Lara Eleen Heckmann
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
  • Luisa Bartram
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
  • Alessa Pabst
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
  • Charlotte Flory
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
  • Maulana Ikhsan
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
  • Sören Pietsch
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
  • Reinhard Schulz
    Wissenschaftliche Werkstätten, University of Lübeck, 23562 Lübeck, Germany.
  • Christopher Kren
    Medical Laser Center Lübeck GmbH, 23562 Lübeck, Germany.
  • Norbert Koop
    Medical Laser Center Lübeck GmbH, 23562 Lübeck, Germany.
  • Johannes Boltze
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
  • Amir Madany Mamlouk
    Institute for Neuro- and Bioinformatics, University of Lübeck, 23562 Lübeck, Germany.
  • Marietta Zille
    Fraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.