Immunoproteasome deficiency results in age-dependent development of epilepsy

Abstract The immunoproteasome is a central protease complex required for optimal antigen presentation. Immunoproteasome activity is also associated with facilitating the degradation of misfolded and oxidized proteins, which prevents cellular stress. While extensively studied during diseases with inc...

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Veröffentlicht in:Brain communications 2024, Vol.6 (1), p.fcae017-fcae017
Hauptverfasser: Leister, Hanna, Krause, Felix F, Gil, Beatriz, Prus, Ruslan, Prus, Inna, Hellhund-Zingel, Anne, Mitra, Meghma, Da Rosa Gerbatin, Rogerio, Delanty, Norman, Beausang, Alan, Brett, Francesca M, Farrell, Michael A, Cryan, Jane, O’Brien, Donncha F, Henshall, David C, Helmprobst, Frederik, Pagenstecher, Axel, Steinhoff, Ulrich, Visekruna, Alexander, Engel, Tobias
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Sprache:eng
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Zusammenfassung:Abstract The immunoproteasome is a central protease complex required for optimal antigen presentation. Immunoproteasome activity is also associated with facilitating the degradation of misfolded and oxidized proteins, which prevents cellular stress. While extensively studied during diseases with increasing evidence suggesting a role for the immunoproteasome during pathological conditions including neurodegenerative diseases, this enzyme complex is believed to be mainly not expressed in the healthy brain. In this study, we show an age-dependent increase in polyubiquitination in the brains of wild-type mice, accompanied by an induction of immunoproteasomes, which was most prominent in neurons and microglia. In contrast, mice completely lacking immunoproteasomes (triple-knockout mice), displayed a strong increase in polyubiquitinated proteins already in the young brain and developed spontaneous epileptic seizures, beginning at the age of 6 months. Injections of kainic acid led to high epilepsy-related mortality of aged triple-knockout mice, confirming increased pathological hyperexcitability states. Notably, the expression of the immunoproteasome was reduced in the brains of patients suffering from epilepsy. In addition, the aged triple-knockout mice showed increased anxiety, tau hyperphosphorylation and degeneration of Purkinje cell population with the resulting ataxic symptoms and locomotion alterations. Collectively, our study suggests a critical role for the immunoproteasome in the maintenance of a healthy brain during ageing. Leister et al. report that immunoproteasome deficiency results in spontaneous seizures and other brain pathologies such as tau hyperphosphorylation, degeneration of Purkinje cells and increased anxiety in aged mice. This suggests that the upregulation of immunoproteasomes during ageing affords protection from the exaggerated accumulation of protein aggregates and epilepsy development. Graphical Abstract Graphical Abstract
ISSN:2632-1297
2632-1297
DOI:10.1093/braincomms/fcae017