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Unfolded protein response markers Grp78 and eIF2alpha are upregulated with increasing alpha-synuclein levels in Lewy body disease
D. Hrabos, I. Poggiolini, L. Civitelli, E. Galli, C. Esapa, M. Saarma, P. Lindholm, L. Parkkinen
Language English Country England, Great Britain
Document type Journal Article
Grant support
PF-IMP-941400
Parkinson's Foundation
MH CZ-DRO (FNOl, 00098892)
Ministry of Health, Czech Republic - conceptual development of research organization
IGA_LF_2024_010
Palacky University Olomouc
IGA_LF_2024_021
Palacky University Olomouc
G-1806
Parkinson's UK - United Kingdom
Weston Brain Institute
MJFF-019580
Michael J. Fox Foundation
NIHR Oxford Biomedical Research Centre
PubMed
39036837
DOI
10.1111/nan.12999
Knihovny.cz E-resources
- MeSH
- alpha-Synuclein * metabolism MeSH
- Biomarkers metabolism MeSH
- Endoplasmic Reticulum Chaperone BiP * metabolism MeSH
- Lewy Body Disease * pathology metabolism MeSH
- Eukaryotic Initiation Factor-2 * metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- Brain metabolism pathology MeSH
- Nerve Growth Factors metabolism MeSH
- Heat-Shock Proteins * metabolism MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Unfolded Protein Response * physiology MeSH
- Endoplasmic Reticulum Stress physiology MeSH
- Up-Regulation * MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
AIMS: Endoplasmic reticulum stress followed by the unfolded protein response is one of the cellular mechanisms contributing to the progression of α-synuclein pathology in Parkinson's disease and other Lewy body diseases. We aimed to investigate the activation of endoplasmic reticulum stress and its correlation with α-synuclein pathology in human post-mortem brain tissue. METHODS: We analysed brain tissue from 45 subjects-14 symptomatic patients with Lewy body disease, 19 subjects with incidental Lewy body disease, and 12 healthy controls. The analysed brain regions included the medulla, pons, midbrain, striatum, amygdala and entorhinal, temporal, frontal and occipital cortex. We analysed activation of endoplasmic reticulum stress via levels of the unfolded protein response-related proteins (Grp78, eIF2α) and endoplasmic reticulum stress-regulating neurotrophic factors (MANF, CDNF). RESULTS: We showed that regional levels of two endoplasmic reticulum-localised neurotrophic factors, MANF and CDNF, did not change in response to accumulating α-synuclein pathology. The concentration of MANF negatively correlated with age in specific regions. eIF2α was upregulated in the striatum of Lewy body disease patients and correlated with increased α-synuclein levels. We found the upregulation of chaperone Grp78 in the amygdala and nigral dopaminergic neurons of Lewy body disease patients. Grp78 levels in the amygdala strongly correlated with soluble α-synuclein levels. CONCLUSIONS: Our data suggest a strong but regionally specific change in Grp78 and eIF2α levels, which positively correlates with soluble α-synuclein levels. Additionally, MANF levels decreased in dopaminergic neurons in the substantia nigra. Our research suggests that endoplasmic reticulum stress activation is not associated with Lewy pathology but rather with soluble α-synuclein concentration and disease progression.
Mammalian Genetics Unit MRC Harwell Institute Harwell Science and Innovation Campus Didcot UK
Nuffield Department of Clinical Neuroscience University of Oxford Oxford UK
References provided by Crossref.org
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