Electromagnetic Modulation of the ALS Transcriptome: Toward a Non-Drug Therapeutic Strategy

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease hallmarked by progressive loss of neuromuscular junctions, cortical and spinal motor neurons (MNs), resulting in muscle paralysis. MNs are particularly vulnerable due to their long axons and high metabolic demands. ALS pathology involves impaired RNA metabolism, protein aggregation, cytoskeletal defects affecting organelle trafficking, and mitochondrial dysfunction, ultimately leading to neurodegeneration. Current treatments only marginally extend survival, calling for alternative therapies. We recently reported beneficial effects of electromagnetic alternating field stimulation (ACMS) on axonal regeneration and organelle motility in ALS. Here, we used iPSC-derived spinal MNs from familial ALS patients with FUS mutations to optimize magnetic field parameters regarding frequency, amplitude and duration. Using compartmentalized neuron cultures, we also tested different magnetic field orientations relative to axons. Following ACMS, we assessed axonal organelle trafficking and the nuclear DNA damage response (DDR) by live-cell imaging. Untreated ALS neurons showed clear defects in both assays. Exposure to magnetic AC sine waves above a threshold amplitude of 7 mT, applied perpendicular to the axonal plane with an optimal low frequency of 25 Hz, led to a sustained boost of mitochondrial and lysosomal motility for over one week and rehabilitation of DDR. These phenotypic improvements correlated with global transcriptomic changes revealed by RNA-sequencing. These phenotypic improvements correlated with global transcriptomic changes revealed by RNA-sequencing. While untreated mutant and wild-type neurons displayed different gene expression profiles, ACMS converged them to a novel, harmonized transcriptional state across all lines. Further analysis of differentially expressed genes (DEGs) yielded a conceptual model in which ACMS activates extracellular matrix (ECM)-mediated cell adhesion and neurotransmitter receptor, ion channel and kinase signaling pathways, ultimately modulating gene transcription and, thereby, motor- and microtubule-associated proteins. This model provides a framework for follow-up studies to experimentally validate the underlying mechanisms and assess the therapeutic potential of ACMS as an alternative biophysical treatment modality for neurodegenerative diseases.

Authors

Institutions

Publication Details

Journal
Cells
Published
2026-11-03
DOI
https://doi.org/10.3390/cells15212003
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Electromagnetic Modulation of the ALS Transcriptome: Toward a Non-Drug Therapeutic Strategy

T. Herrmannsdörfer, Jonas Gronemann, Richard H. W. Funk, Julia Japtok et al.
Cells
Amyotrophic Lateral Sclerosis Research
article

Electromagnetic Modulation of the ALS Transcriptome: Toward a Non-Drug Therapeutic Strategy

T. Herrmannsdörfer, Jonas Gronemann, Richard H. W. Funk, Julia Japtok, M. Uhlarz, Banaja P. Dash, Andreas Dahl, Arun Pal, Andreas Hermann, J. Wosnitza, Katrin Sameith, Hannes Glaß, Jens Pietzsch
article en

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease hallmarked by progressive loss of neuromuscular junctions, cortical and spinal motor neurons (MNs), resulting in muscle paralysis. MNs are particularly vulnerable due to their long axons and high metabolic demands. ALS pathology involves impaired RNA metabolism, protein aggregation, cytoskeletal defects affecting organelle trafficking, and mitochondrial dysfunction, ultimately leading to neurodegeneration. Current treatments only marginally extend survival, calling for alternative therapies. We recently reported beneficial effects of electromagnetic alternating field stimulation (ACMS) on axonal regeneration and organelle motility in ALS. Here, we used iPSC-derived spinal MNs from familial ALS patients with FUS mutations to optimize magnetic field parameters regarding frequency, amplitude and duration. Using compartmentalized neuron cultures, we also tested different magnetic field orientations relative to axons. Following ACMS, we assessed axonal organelle trafficking and the nuclear DNA damage response (DDR) by live-cell imaging. Untreated ALS neurons showed clear defects in both assays. Exposure to magnetic AC sine waves above a threshold amplitude of 7 mT, applied perpendicular to the axonal plane with an optimal low frequency of 25 Hz, led to a sustained boost of mitochondrial and lysosomal motility for over one week and rehabilitation of DDR. These phenotypic improvements correlated with global transcriptomic changes revealed by RNA-sequencing. These phenotypic improvements correlated with global transcriptomic changes revealed by RNA-sequencing. While untreated mutant and wild-type neurons displayed different gene expression profiles, ACMS converged them to a novel, harmonized transcriptional state across all lines. Further analysis of differentially expressed genes (DEGs) yielded a conceptual model in which ACMS activates extracellular matrix (ECM)-mediated cell adhesion and neurotransmitter receptor, ion channel and kinase signaling pathways, ultimately modulating gene transcription and, thereby, motor- and microtubule-associated proteins. This model provides a framework for follow-up studies to experimentally validate the underlying mechanisms and assess the therapeutic potential of ACMS as an alternative biophysical treatment modality for neurodegenerative diseases.

CellsVol. 15(21)
German Center for Neurodegenerative Diseases (DE), Helmholtz-Zentrum Dresden-Rossendorf (DE), Dresden International University (DE), Universitätsmedizin Rostock (DE), Max Planck Institute of Molecular Cell Biology and Genetics (DE), DRESDEN-concept Genome Center (DE), Dresden High Magnetic Field Laboratory (DE), Center for Molecular and Cellular Bioengineering (DE), University of Rostock (DE), Technische Universität Dresden (DE)
Openalex Percentile: Top 16%
Amyotrophic Lateral Sclerosis Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon