Evidence map›Paper›PMID 34685519›Full record

ArticleCells2021

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

Alex Palumbo, Philipp Grüning, Svenja Kim Landt, Lara Eleen Heckmann, Luisa Bartram, Alessa Pabst, Charlotte Flory, Maulana Ikhsan, Sören Pietsch, Reinhard Schulz and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 4 countries.

Alex PalumboFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.ORCID 0000-0002-1631-785X
Philipp GrüningInstitute for Neuro- and Bioinformatics, University of Lübeck, 23562 Lübeck, Germany.ORCID 0000-0003-2946-4020
Svenja Kim LandtFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
Lara Eleen HeckmannFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.ORCID 0000-0003-1264-9715
Luisa BartramFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
Alessa PabstFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.ORCID 0000-0003-1938-3753
Charlotte FloryFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.ORCID 0000-0001-5049-6380
Maulana IkhsanFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
Sören PietschFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
Reinhard SchulzWissenschaftliche Werkstätten, University of Lübeck, 23562 Lübeck, Germany.
Christopher KrenMedical Laser Center Lübeck GmbH, 23562 Lübeck, Germany.
Norbert KoopMedical Laser Center Lübeck GmbH, 23562 Lübeck, Germany.
Johannes BoltzeFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.
Amir Madany MamloukInstitute for Neuro- and Bioinformatics, University of Lübeck, 23562 Lübeck, Germany.ORCID 0000-0001-9709-1620
Marietta ZilleFraunhofer Research and Development Center for Marine and Cellular Biotechnology EMB, 23562 Lübeck, Germany.ORCID 0000-0002-0609-8956
Fraunhofer Research Institution for Individualized and Cell-Based Medical Engineering · DEUniversity of Lübeck · DEMedizinisches Laserzentrum Lübeck (Germany) · DEMalikussaleh University · IDUniversity Hospital Leipzig · DEUniversity of Vienna · ATUniversity of Warwick · GB

Funding

Fraunhofer-Gesellschaft 600199Joachim Herz Stiftung 850022
6 · The paper itself

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.

Indexed as

Deep LearningAnimalsAxonsCell DeathDisease Models, AnimalHumansNerve DegenerationNeurodegenerative DiseasesNeuronsaxonbrain hemorrhagecell culturecortical neuronsmachine learningmicrofluidicmicroscopystroketime-lapse

Identifiers

PMID34685519
PMCPMC8534012
OpenAlexW3203450828

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.