Evidence map›Paper›PMID 38317856›Full record

ArticleBrain communications2024

Immunoproteasome deficiency results in age-dependent development of epilepsy.

Hanna Leister, Felix F Krause, Beatriz Gil, Ruslan Prus, Inna Prus, Anne Hellhund-Zingel, Meghma Mitra, Rogerio Da Rosa Gerbatin, Norman Delanty, Alan Beausang and 10 more

Open access · goldAbstract read
In one paragraph

Article in Brain communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. The Role of the Ubiquitin System in Eye Diseases.Life (Basel, Switzerland) · 2025
    Review
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 4 institutions in 2 countries.

Hanna LeisterInstitute for Medical Microbiology and Hygiene, Philipps-University, 35043 Marburg, Germany.
Felix F KrauseInstitute for Medical Microbiology and Hygiene, Philipps-University, 35043 Marburg, Germany.
Beatriz GilDepartment of Physiology and Medical Physics, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, D02 YN77 Dublin, Ireland.
Ruslan PrusDepartment of Physiology and Medical Physics, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, D02 YN77 Dublin, Ireland.
Inna PrusDepartment of Physiology and Medical Physics, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, D02 YN77 Dublin, Ireland.
Anne Hellhund-ZingelInstitute for Medical Microbiology and Hygiene, Philipps-University, 35043 Marburg, Germany.
Meghma MitraDepartment of Physiology and Medical Physics, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, D02 YN77 Dublin, Ireland.
Rogerio Da Rosa GerbatinFutureNeuro, SFI Research Centre for Chronic and Rare Neurological Diseases, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, D02 YN77 Dublin, Ireland.
Norman DelantyFutureNeuro, SFI Research Centre for Chronic and Rare Neurological Diseases, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, D02 YN77 Dublin, Ireland.
Alan BeausangDepartment of Neuropathology, Beaumont Hospital, D09V2N0 Dublin, Ireland.
Francesca M BrettDepartment of Neuropathology, Beaumont Hospital, D09V2N0 Dublin, Ireland.
Michael A FarrellDepartment of Neuropathology, Beaumont Hospital, D09V2N0 Dublin, Ireland.ORCID https://orcid.org/0000-0001-5864-3357
Jane CryanDepartment of Neuropathology, Beaumont Hospital, D09V2N0 Dublin, Ireland.
Donncha F O'BrienDepartment of Neurosurgery, Beaumont Hospital, D09V2N0 Dublin, Ireland.
David C HenshallDepartment of Physiology and Medical Physics, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, D02 YN77 Dublin, Ireland.
Frederik HelmprobstInstitute of Neuropathology, Philipps-University, 35043 Marburg, Germany.
Axel PagenstecherInstitute of Neuropathology, Philipps-University, 35043 Marburg, Germany.
Ulrich SteinhoffInstitute for Medical Microbiology and Hygiene, Philipps-University, 35043 Marburg, Germany.
Alexander VisekrunaInstitute for Medical Microbiology and Hygiene, Philipps-University, 35043 Marburg, Germany.ORCID https://orcid.org/0000-0002-5207-9545
Tobias EngelDepartment of Physiology and Medical Physics, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, D02 YN77 Dublin, Ireland.
Royal College of Surgeons in Ireland · IEBeaumont Hospital · IEInstitute of Medical Microbiology and Hygiene · DEPhilipps University of Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

ageingbrainepilepsyimmunoproteasome

Identifiers

PMID38317856
PMCPMC10839634
OpenAlexW4391324423

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.