Single-nucleus multiome shows motor neuron glutamate overactivation in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that causes motor neuron degeneration. However, the mechanisms underlying the selective vulnerability of motor neurons and the involvement of non-motor neuron cells in ALS remain unclear. To investigate ALS pathology at the cellular level, we performed a single-nucleus multiome analysis, including RNA sequencing and chromatin accessibility profiling, on motor cortex (75,583 nuclei) and spinal cord (62,711 nuclei) from patients with ALS (n=6) and controls (n=6). Our results revealed significant gene expression changes specifically in spinal motor neurons, including upregulation of a metabotropic glutamate receptor, GRM5, and enhanced glutamate signaling. By integrating genome-wide association study data, we identified ALS-associated SNPs in regulatory regions, suggesting cell-type-specific enrichment of risk, especially in microglia. These findings suggest that changes in spinal motor neurons and their surrounding environment, including glutamate signaling, may be involved in ALS pathology. The study also provides valuable resources for future research on the underlying mechanisms and potential therapeutic targets.

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Publication Details

Journal
Brain
Published
2025-11-11
DOI
https://doi.org/10.1093/brain/awaf426
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Single-nucleus multiome shows motor neuron glutamate overactivation in amyotrophic lateral sclerosis

Goichi Beck, Daisuke Motooka, Kohji Mori, Daisuke Okuzaki et al.
Brain
Amyotrophic Lateral Sclerosis Research
article

Single-nucleus multiome shows motor neuron glutamate overactivation in amyotrophic lateral sclerosis

Goichi Beck, Daisuke Motooka, Kohji Mori, Daisuke Okuzaki, Kotaro Ogawa, Yoshiaki Yasumizu, Shigeo Murayama, Yasuki Ishihara, Yoshihiro Asano, Hideki Mochizuki, Eiichi Morii, Junko Morita, Seiichi Nagano, Yohei Miyashita, Yuko Saito, Masakazu Ishikawa, Miho Nagata, E. Takeuchi
article en

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that causes motor neuron degeneration. However, the mechanisms underlying the selective vulnerability of motor neurons and the involvement of non-motor neuron cells in ALS remain unclear. To investigate ALS pathology at the cellular level, we performed a single-nucleus multiome analysis, including RNA sequencing and chromatin accessibility profiling, on motor cortex (75,583 nuclei) and spinal cord (62,711 nuclei) from patients with ALS (n=6) and controls (n=6). Our results revealed significant gene expression changes specifically in spinal motor neurons, including upregulation of a metabotropic glutamate receptor, GRM5, and enhanced glutamate signaling. By integrating genome-wide association study data, we identified ALS-associated SNPs in regulatory regions, suggesting cell-type-specific enrichment of risk, especially in microglia. These findings suggest that changes in spinal motor neurons and their surrounding environment, including glutamate signaling, may be involved in ALS pathology. The study also provides valuable resources for future research on the underlying mechanisms and potential therapeutic targets.

Brain
Osaka Gakuin University (JP), Yale University (US), Toneyama National Hospital (JP), NeuroDevelopment Center (US), National Cerebral and Cardiovascular Center (JP), Tokyo Metropolitan Institute of Gerontology (JP), Tokyo Metropolitan Geriatric Hospital (JP), The University of Osaka (JP)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science, Cybermedia Center, Osaka University, Research Institute for Microbial Diseases, Osaka University
Openalex Percentile: Top 53%
Amyotrophic Lateral Sclerosis Research
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