Scientific ReportsNeurosciencePeer-reviewed journal article
NMJ-Analyser: high-throughput morphological screening of neuromuscular junctions identifies subtle changes in mouse neuromuscular disease models
Alan Mejia MazaiD, Seth Jarvis, Weaverly Colleen LeeiD, Thomas J. CunninghamiD, Giampietro SchiavoiD, Maria SecrieriD, Pietro FrattaiD, James N. SleighiD, Elizabeth FisheriD, Carole H. SudreiD
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.
- organism: mouse
- assay: imaging
- research focus: cell type annotation
- approach: machine learning (classical)
- Citations
- 30
- FWCI
- 2.63
- Field percentile
- top 8%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Scalable, optically-responsive human neuromuscular junction model reveals convergent mechanisms of synaptic dysfunction in familial ALS
Daniel Chen, Polyxeni Philippidou, … Helen C. Miranda·bioRxiv·Jan 11, 2024
- Post-synaptic morphology of mouse neuromuscular junctions is linked to muscle fibre type
Aleksandra M. Mech, Anna‐Leigh Brown, … James N. Sleigh·Journal of AnatomyPeer-reviewed·Jun 13, 2020
- Structural and functional alterations of neuromuscular synapses in a mouse model of ACTA1 congenital myopathy
Yun Liu, Weichun Lin·bioRxiv·Feb 23, 2022
- Comparison of neuromuscular junction dynamics following ischemic and aged skeletal muscle
Berna Aliya, Mahir Mohiuddin, … Young Charles Jang·bioRxiv·Nov 23, 2021
- Properties of Glial Cell at the Neuromuscular Junction are Incompatible with synaptic repair in the SOD1G37R ALS mouse model
Éric Martineau, Danielle Arbour, … Richard Robitaille·Journal of NeurosciencePeer-reviewed·Aug 28, 2020
- A standardized framework resolves ambiguity in motor neuron loss across neurodegenerative diseases
Leonie Sowoidnich, Aaron L. Norman, … Christian M. Simon·Acta Neuropathologica CommunicationsPeer-reviewed·Sep 1, 2026