NMJ-Analyser identifies subtle early changes in mouse models of neuromuscular disease.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
10 06 2021
Historique:
received: 21 09 2020
accepted: 26 04 2021
entrez: 11 6 2021
pubmed: 12 6 2021
medline: 28 10 2021
Statut: epublish

Résumé

The neuromuscular junction (NMJ) is the peripheral synapse formed between a motor neuron axon terminal and a muscle fibre. NMJs are thought to be the primary site of peripheral pathology in many neuromuscular diseases, but innervation/denervation status is often assessed qualitatively with poor systematic criteria across studies, and separately from 3D morphological structure. Here, we describe the development of 'NMJ-Analyser', to comprehensively screen the morphology of NMJs and their corresponding innervation status automatically. NMJ-Analyser generates 29 biologically relevant features to quantitatively define healthy and aberrant neuromuscular synapses and applies machine learning to diagnose NMJ degeneration. We validated this framework in longitudinal analyses of wildtype mice, as well as in four different neuromuscular disease models: three for amyotrophic lateral sclerosis (ALS) and one for peripheral neuropathy. We showed that structural changes at the NMJ initially occur in the nerve terminal of mutant TDP43 and FUS ALS models. Using a machine learning algorithm, healthy and aberrant neuromuscular synapses are identified with 95% accuracy, with 88% sensitivity and 97% specificity. Our results validate NMJ-Analyser as a robust platform for systematic and structural screening of NMJs, and pave the way for transferrable, and cross-comparison and high-throughput studies in neuromuscular diseases.

Identifiants

pubmed: 34112844
doi: 10.1038/s41598-021-91094-6
pii: 10.1038/s41598-021-91094-6
pmc: PMC8192785
doi:

Substances chimiques

Biomarkers 0
FUS protein, mouse 0
RNA-Binding Protein FUS 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

12251

Subventions

Organisme : Medical Research Council
ID : MR/M008606/1
Pays : United Kingdom
Organisme : Motor Neurone Disease Association
ID : FRATTA/JAN15/946-795
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 107116/Z/15/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S006990/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S006508/1
Pays : United Kingdom
Organisme : Motor Neurone Disease Association
ID : FISHER/APR14/874-792
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_EX_MR/N501931/1
Pays : United Kingdom
Organisme : Motor Neurone Disease Association
ID : PLAGNOL/OCT15/885-792
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L021056/1
Pays : United Kingdom
Organisme : EPA
ID : EP-W-17-011
Pays : United States
Organisme : Medical Research Council
ID : G0801110
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 215296/Z/19/Z
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom

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Auteurs

Alan Mejia Maza (A)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.

Seth Jarvis (S)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.

Weaverly Colleen Lee (WC)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.

Thomas J Cunningham (TJ)

Mammalian Genetics Unit, MRC Harwell Institute, Oxfordshire, OX11 0RD, UK.

Giampietro Schiavo (G)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.
UK Dementia Research Institute, University College London, London, WC1E 6BT, UK.

Maria Secrier (M)

Department of Genetics, Evolution and Environment, UCL Genetic Institute, University College London, London, WC1E 6BT, UK.

Pietro Fratta (P)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.

James N Sleigh (JN)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.
UK Dementia Research Institute, University College London, London, WC1E 6BT, UK.

Elizabeth M C Fisher (EMC)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.

Carole H Sudre (CH)

MRC Unit for Lifelong Health and Ageing, Department of Population Science and Experimental Medicine, University College London, London, WC1E 6BT, UK. c.sudre@ucl.ac.uk.
Centre for Medical Image Computing, Department of Computer Science, University College London, London, WC1E 6BT, UK. c.sudre@ucl.ac.uk.
School of Biomedical Engineering and Imaging Sciences, King's College London, London, W2CR 2LS, UK. c.sudre@ucl.ac.uk.

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