Acta Neuropathologica CommunicationsNeurosciencePeer-reviewed journal article
A standardized framework resolves ambiguity in motor neuron loss across neurodegenerative diseases
Leonie Sowoidnich, Aaron L. Norman, Florian GerstneriD, Josiane K. Siemund, Jannik M. Buettner, John G. PagiazitisiD, Vanessa Dreilich, Konstantin Pilz, Dajun TianiD, Charlotte J. SumneriD, Angela Paradis, George Z. MentisiD, Christian M. SimoniD
Abstract
Motor neuron (MN) loss is a hallmark of neurodegenerative disorders, yet its assessment remains variable, confounding mechanistic and therapeutic interpretation. To address this, we conducted a systematic review and meta-analysis of spinal muscular atrophy (SMA) mouse studies, revealing 60% variability in reported MN loss, largely attributable to nonspecific spinal cord sampling. Using a whole-segment approach with tissue clearing, MN tracing, and multimodal imaging, we confirmed segment-dependent differences in MN counts. Common MN markers (SMI-32, Nissl) lacked specificity, whereas choline acetyltransferase (ChAT) provided robust labeling in murine and human spinal cords. Deep learning-based whole-mount segmentation enabled unbiased MN quantification and validated manual counts. Integrating analysis with computational modeling established segment sampling as a key driver of variability and revealed degeneration patterns: widespread MN loss in amyotrophic lateral sclerosis (ALS), selective MN loss in severe SMA, and preservation in mild SMA models. These findings establish a framework for reproducible MN quantification. HighlightsO_LISpinal cord segment-specific analysis reduces variability and allows accurate MN quantification C_LIO_LIChAT is the most reliable MN marker in murine and human spinal cords C_LIO_LIDeep learning-based segmentation enables unbiased MN quantification in intact spinal cords C_LIO_LIMN degeneration is widespread in ALS but restricted to pools innervating proximal muscles in severe SMA C_LI
- organism: mouse
- assay: imaging
- research focus: cell type annotation
- approach: statistical model
- approach: deep learning
- Citations
- 1
- FWCI
- 1.31
- Field percentile
- top 25%
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
- Neuromuscular denervation and deafferentation but not motor neuron death are disease features in the Smn 2B/- mouse model of SMA
Maria Jose Carlini, Marina K Triplett, Livio Pellizzoni·PLoS ONEPeer-reviewed·Aug 1, 2022
- Caudal-rostral progression of alpha motoneurone degeneration in the SOD1G93A mouse model of amyotrophic lateral sclerosis
Alastair J. Kirby, Thomas Palmer, … Samit Chakrabarty·bioRxiv·Jun 27, 2020
- NMJ-Analyser: high-throughput morphological screening of neuromuscular junctions identifies subtle changes in mouse neuromuscular disease models
Alan Mejia Maza, Seth Jarvis, … Carole H. Sudre·Scientific ReportsPeer-reviewed·Jun 10, 2021
- Age-dependent peripheral nerve and Schwann cell abnormalities in a mouse model of late-onset spinal muscular atrophy
Kai Christine Liebig, Nicola Bense, … Tim Hagenacker·bioRxiv·Jul 30, 2026
- Spinal inhibitory neurons degenerate before motor neurons and excitatory neurons in a mouse model of ALS
Roser Montañana-Rosell, Raghavendra Selvan, … Ilary Allodi·Science AdvancesPeer-reviewed·May 31, 2024
- Skeletal muscle MRI differentiates SBMA and ALS and correlates with disease severity
Uros Klickovic, Luca Zampedri, … Pietro Fratta·NeurologyPeer-reviewed·Aug 7, 2019