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Human Motor Neurons Elicit Pathological Hallmarks of ALS and Reveal Potential Biomarkers of the Disease in Response to Prolonged IFNγ Exposure.
Chun, Changho; Lee, Jung Hyun; Bothwell, Mark; Nghiem, Paul; Smith, Alec S T; Mack, David L.
Afiliación
  • Chun C; Departments of Bioengineering, University of Washington, Seattle, Washington 98195.
  • Lee JH; Rehabilitation Medicine, University of Washington, Seattle, Washington 98195.
  • Bothwell M; Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109.
  • Nghiem P; Departments of Dermatology, School of Medicine, University of Washington, Seattle, Washington 98195.
  • Smith AST; Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109.
  • Mack DL; Physiology & Biophysics, University of Washington, Seattle, Washington 98195.
J Neurosci ; 44(16)2024 Apr 17.
Article en En | MEDLINE | ID: mdl-38413232
ABSTRACT
Amyotrophic lateral sclerosis (ALS) is a debilitating neurodegenerative disorder marked by progressive motor neuron degeneration and muscle denervation. A recent transcriptomic study integrating a wide range of human ALS samples revealed that the upregulation of p53, a downstream target of inflammatory stress, is commonly detected in familial and sporadic ALS cases by a mechanism linked to a transactive response DNA-binding protein 43 (TDP-43) dysfunction. In this study, we show that prolonged interferon-gamma (IFNγ) treatment of human induced pluripotent stem cell-derived spinal motor neurons results in a severe cytoplasmic aggregation of TDP-43. TDP-43 dysfunction resulting from either IFNγ exposure or an ALS-associated TDP-43 mutation was associated with the activation of the p53 pathway. This was accompanied by the hyperactivation of neuronal firing, followed by the complete loss of their electrophysiological function. Through a comparative single-cell transcriptome analysis, we have identified significant alterations in ALS-associated genes in motor neurons exposed to IFNγ, implicating their direct involvement in ALS pathology. Interestingly, IFNγ was found to induce significant levels of programmed death-ligand 1 (PD-L1) expression in motor neurons without affecting the levels of any other immune checkpoint proteins. This finding suggests a potential role of excessive PD-L1 expression in ALS development, given that PD-L1 was recently reported to impair neuronal firing ability in mice. Our findings suggest that exposing motor neurons to IFNγ could directly derive ALS pathogenesis, even without the presence of the inherent genetic mutation or functional glia component. Furthermore, this study provides a comprehensive list of potential candidate genes for future immunotherapeutic targets with which to treat sporadic forms of ALS, which account for 90% of all reported cases.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Pluripotentes Inducidas / Esclerosis Amiotrófica Lateral Límite: Animals / Humans Idioma: En Revista: J Neurosci Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Pluripotentes Inducidas / Esclerosis Amiotrófica Lateral Límite: Animals / Humans Idioma: En Revista: J Neurosci Año: 2024 Tipo del documento: Article