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NMJ-Analyser identifies subtle early changes in mouse models of neuromuscular disease.
Mejia Maza, Alan; Jarvis, Seth; Lee, Weaverly Colleen; Cunningham, Thomas J; Schiavo, Giampietro; Secrier, Maria; Fratta, Pietro; Sleigh, James N; Fisher, Elizabeth M C; Sudre, Carole H.
Afiliação
  • Mejia Maza A; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.
  • Jarvis S; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.
  • Lee WC; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.
  • Cunningham TJ; Mammalian Genetics Unit, MRC Harwell Institute, Oxfordshire, OX11 0RD, UK.
  • Schiavo G; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.
  • Secrier M; UK Dementia Research Institute, University College London, London, WC1E 6BT, UK.
  • Fratta P; Department of Genetics, Evolution and Environment, UCL Genetic Institute, University College London, London, WC1E 6BT, UK.
  • Sleigh JN; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.
  • Fisher EMC; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.
  • Sudre CH; UK Dementia Research Institute, University College London, London, WC1E 6BT, UK.
Sci Rep ; 11(1): 12251, 2021 06 10.
Article em En | MEDLINE | ID: mdl-34112844
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neuromusculares / Junção Neuromuscular Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Animals Idioma: En Revista: Sci Rep Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neuromusculares / Junção Neuromuscular Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Animals Idioma: En Revista: Sci Rep Ano de publicação: 2021 Tipo de documento: Article