Endoplasmic Reticulum Stress in Neurodegenerative Diseases

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cells of the Nervous System".

Deadline for manuscript submissions: 15 September 2024 | Viewed by 2883

Special Issue Editors


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Guest Editor
Department of Biochemistry and Developmental Biology, Faculty of Medicine, University of Helsinki, FIN-00014 Helsinki, Finland
Interests: neuroscience; neurodegeneration; ER stress

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Guest Editor
Institute of Biotechnology, HiLIFE, University of Helsinki, Viikinkaari 5D, 00790 Helsinki, Finland
Interests: neurotrophic factors; growth factor signaling; cell death; neurodegeneration; animal models; Parkinson’s disease

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Guest Editor
Institute of Biotechnology, HiLIFE, University of Helsinki, Helsinki, Finland
Interests: neurotrophic factors; neurodegeneration; ER stress; UPR

Special Issue Information

Dear Colleagues,

Disturbed protein homeostasis is associated with several neurodegenerative disorders such as Parkinson’s disease, Huntington’s disease, amyotrophic lateral sclerosis, and Alzheimer’s disease, among others. In these disorders, there is an accumulation of misfolded proteins in brain cells leading to counterbalancing signaling including the activation of the unfolded protein response in the endoplasmic reticulum (ER) with the aim to restore homeostasis. However, when prolonged or accentuated, ER stress itself is maladaptive and causes defects in protein turnover, calcium and metabolic dysfunctions, increased oxidative stress, and inflammation responses in the brain ultimately leading to cell death. The precise roles of ER stress in the pathogenesis of the neurodegenerative diseases and the mechanisms how ER stress triggers cell death are, however, not fully understood.

In this Special Issue, a collection of papers by distinguished scientists in the field is presented. ER stress will be discussed from different points of view elucidating both its pathophysiology, the signaling mechanisms involved and the possibilities to interfere with and alleviate the consequences of enhanced ER stress in the different diseases. In addition to protein homeostasis, the emerging roles of ER stress in the regulation of RNA and metabolism will also be highlighted. Together, these results underscore the importance of ER stress and its signaling pathways regulating protein homeostasis to meet various challenges that brain cells encounter during normal life, and which contribute to neurodegenerative disorders and brain ageing. An increased understanding of the mechanisms of ER stress and their relationship with other cellular signaling pathways in brain cells and in various neurodegenerative disorders is crucial for the development of better therapies for these diseases.

Prof. Dr. Dan Lindholm
Prof. Dr. Mart Saarma
Dr. Vera Kovaleva
Guest Editors

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Keywords

  • endoplasmic reticulum
  • ER stress
  • Parkinson’s disease
  • Huntington’s disease
  • amyotrophic lateral sclerosis
  • Alzheimer’s disease
  • neurodegenerative disorders

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Published Papers (2 papers)

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Research

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17 pages, 4216 KiB  
Article
An Essential Role for Calnexin in ER-Phagy and the Unfolded Protein Response
by Daniel Wolf, Chiara Röder, Michael Sendtner and Patrick Lüningschrör
Cells 2024, 13(17), 1498; https://doi.org/10.3390/cells13171498 - 6 Sep 2024
Abstract
ER-phagy is a specialized form of autophagy, defined by the lysosomal degradation of ER subdomains. ER-phagy has been implicated in relieving the ER from misfolded proteins during ER stress upon activation of the unfolded protein response (UPR). Here, we identified an essential role [...] Read more.
ER-phagy is a specialized form of autophagy, defined by the lysosomal degradation of ER subdomains. ER-phagy has been implicated in relieving the ER from misfolded proteins during ER stress upon activation of the unfolded protein response (UPR). Here, we identified an essential role for the ER chaperone calnexin in regulating ER-phagy and the UPR in neurons. We showed that chemical induction of ER stress triggers ER-phagy in the somata and axons of primary cultured motoneurons. Under basal conditions, the depletion of calnexin leads to an enhanced ER-phagy in axons. However, upon ER stress induction, ER-phagy did not further increase in calnexin-deficient motoneurons. In addition to increased ER-phagy under basal conditions, we also detected an elevated proteasomal turnover of insoluble proteins, suggesting enhanced protein degradation by default. Surprisingly, we detected a diminished UPR in calnexin-deficient early cortical neurons under ER stress conditions. In summary, our data suggest a central role for calnexin in orchestrating both ER-phagy and the UPR to maintain protein homeostasis within the ER. Full article
(This article belongs to the Special Issue Endoplasmic Reticulum Stress in Neurodegenerative Diseases)
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Review

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32 pages, 1753 KiB  
Review
Protein Quality Control Systems and ER Stress as Key Players in SARS-CoV-2-Induced Neurodegeneration
by Elena Gavilán, Rafael Medina-Guzman, Bazhena Bahatyrevich-Kharitonik and Diego Ruano
Cells 2024, 13(2), 123; https://doi.org/10.3390/cells13020123 - 9 Jan 2024
Cited by 4 | Viewed by 2405
Abstract
The COVID-19 pandemic has brought to the forefront the intricate relationship between SARS-CoV-2 and its impact on neurological complications, including potential links to neurodegenerative processes, characterized by a dysfunction of the protein quality control systems and ER stress. This review article explores the [...] Read more.
The COVID-19 pandemic has brought to the forefront the intricate relationship between SARS-CoV-2 and its impact on neurological complications, including potential links to neurodegenerative processes, characterized by a dysfunction of the protein quality control systems and ER stress. This review article explores the role of protein quality control systems, such as the Unfolded Protein Response (UPR), the Endoplasmic Reticulum-Associated Degradation (ERAD), the Ubiquitin–Proteasome System (UPS), autophagy and the molecular chaperones, in SARS-CoV-2 infection. Our hypothesis suggests that SARS-CoV-2 produces ER stress and exploits the protein quality control systems, leading to a disruption in proteostasis that cannot be solved by the host cell. This disruption culminates in cell death and may represent a link between SARS-CoV-2 and neurodegeneration. Full article
(This article belongs to the Special Issue Endoplasmic Reticulum Stress in Neurodegenerative Diseases)
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