Cytoskeletal disruption-induced calcium dysregulation drives cell death in anti-IgLON5 disease

Anti-IgLON5 disease is an autoimmune encephalitis with more chronic presentation including memory decline, sleep disorder, bulbar symptoms and movement disorder. Post-mortem brains of patients with anti-IgLON5 disease show neurodegeneration with tau deposition sparking interest in this 'acquired tauopathy' as a disease model for neurodegeneration, yet mechanisms of neurodegeneration remain unknown. Using a reductionist human iPSC-derived neuron-antibody model, we applied proteomics approach, electrophysiology and live cell imaging. iNeurons treated with anti-IgLON5 IgG presented with cytoskeletal disruption along with tau depositions, which correlated with endophenotypes. Accompanying calcium dysregulation was driven by impaired ER refill and mitochondrial dysfunction leading to cell death. Analogous cytoskeletal disruption is also reflected in the serum of treatment naïve patients using OLink proteomics. These findings provide insight into anti-IgLON5 disease pathology and pinpoint downstream signalling events of direct antibody-neuron interactions, which involve novel targets such as cytoskeletal disruption along with calcium dysregulation.

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Publication Details

Journal
Redox Biology
Published
2025-09-04
DOI
https://doi.org/10.1016/j.redox.2025.103854
Citations
1
Primary Topic
Autoimmune Neurological Disorders and Treatments
Type
article
Field-Weighted Citation Impact
1.39

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article

Cytoskeletal disruption-induced calcium dysregulation drives cell death in anti-IgLON5 disease

Júlia Csatári, Jan D. Lünemann, Laura Vinnenberg, Nadine Ritter et al.
1 citations
Redox Biology
Autoimmune Neurological Disorders and Treatments
1.39
article

Cytoskeletal disruption-induced calcium dysregulation drives cell death in anti-IgLON5 disease

Júlia Csatári, Jan D. Lünemann, Laura Vinnenberg, Nadine Ritter, Isabel Aymanns, Petra Hundehege, Matthias Pawlowski, Andreas Schulte‐Mecklenbeck, Lisanne Korn, Thilo Kaehne, Stjepana Kovac, Guiscard Seebohm, Paul Disse, Catharina C. Gross, Heinz Wiendl
article en
1 citations

Abstract

Anti-IgLON5 disease is an autoimmune encephalitis with more chronic presentation including memory decline, sleep disorder, bulbar symptoms and movement disorder. Post-mortem brains of patients with anti-IgLON5 disease show neurodegeneration with tau deposition sparking interest in this 'acquired tauopathy' as a disease model for neurodegeneration, yet mechanisms of neurodegeneration remain unknown. Using a reductionist human iPSC-derived neuron-antibody model, we applied proteomics approach, electrophysiology and live cell imaging. iNeurons treated with anti-IgLON5 IgG presented with cytoskeletal disruption along with tau depositions, which correlated with endophenotypes. Accompanying calcium dysregulation was driven by impaired ER refill and mitochondrial dysfunction leading to cell death. Analogous cytoskeletal disruption is also reflected in the serum of treatment naïve patients using OLink proteomics. These findings provide insight into anti-IgLON5 disease pathology and pinpoint downstream signalling events of direct antibody-neuron interactions, which involve novel targets such as cytoskeletal disruption along with calcium dysregulation.

Redox BiologyVol. 86
Düsseldorf University Hospital (DE), University Hospital Münster (DE), Heinrich Heine University Düsseldorf (DE), Otto-von-Guericke-Universität Magdeburg (DE)
Deutsche Forschungsgemeinschaft, Westfälische Wilhelms-Universität Münster
Openalex Percentile: Top 16%
Autoimmune Neurological Disorders and Treatments
1.39
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