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Increased MANF Expression in the Inferior Temporal Gyrus in Patients With Alzheimer Disease
Alzheimer disease (AD) is an aging-related disorder linked to endoplasmic reticulum (ER) stress. The main pathologic feature of AD is the presence of extracellular senile plaques and intraneuronal neurofibrillary tangles (NFTs) in the brain. In neurodegenerative diseases, the unfolded protein respon...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117094/ https://www.ncbi.nlm.nih.gov/pubmed/33994992 http://dx.doi.org/10.3389/fnagi.2021.639318 |
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author | Liu, Xue-Chun Qi, Xiu-Hong Fang, Hui Zhou, Ke-Qing Wang, Qing-Song Chen, Gui-Hai |
author_facet | Liu, Xue-Chun Qi, Xiu-Hong Fang, Hui Zhou, Ke-Qing Wang, Qing-Song Chen, Gui-Hai |
author_sort | Liu, Xue-Chun |
collection | PubMed |
description | Alzheimer disease (AD) is an aging-related disorder linked to endoplasmic reticulum (ER) stress. The main pathologic feature of AD is the presence of extracellular senile plaques and intraneuronal neurofibrillary tangles (NFTs) in the brain. In neurodegenerative diseases, the unfolded protein response (UPR) induced by ER stress ensures cell survival. Mesencephalic astrocyte-derived neurotrophic factor (MANF) protects against ER stress and has been implicated in the pathogenesis of AD. MANF is expressed in neurons of the brain and spinal cord. However, there have been no investigations on MANF expression in the brain of AD patients. This was addressed in the present study by immunohistochemistry, western blotting, and quantitative analyses of postmortem brain specimens. We examined the localization and expression levels of MANF in the inferior temporal gyrus of the cortex (ITGC) in AD patients (n = 5), preclinical (pre-)AD patients (n = 5), and age-matched non-dementia controls (n = 5) by double immunofluorescence labeling with antibodies against the neuron-specific nuclear protein neuronal nuclei (NeuN), ER chaperone protein 78-kDa glucose-regulated protein (GRP78), and MANF. The results showed that MANF was mainly expressed in neurons of the ITGC in all 3 groups; However, the number of MANF-positive neurons was significantly higher in pre-AD (Braak stage III/IV) and AD (Braak stage V/VI) patients than that in the control group. Thus, MANF is overexpressed in AD and pre-AD, suggesting that it can serve as a diagnostic marker for early stage disease. |
format | Online Article Text |
id | pubmed-8117094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81170942021-05-14 Increased MANF Expression in the Inferior Temporal Gyrus in Patients With Alzheimer Disease Liu, Xue-Chun Qi, Xiu-Hong Fang, Hui Zhou, Ke-Qing Wang, Qing-Song Chen, Gui-Hai Front Aging Neurosci Neuroscience Alzheimer disease (AD) is an aging-related disorder linked to endoplasmic reticulum (ER) stress. The main pathologic feature of AD is the presence of extracellular senile plaques and intraneuronal neurofibrillary tangles (NFTs) in the brain. In neurodegenerative diseases, the unfolded protein response (UPR) induced by ER stress ensures cell survival. Mesencephalic astrocyte-derived neurotrophic factor (MANF) protects against ER stress and has been implicated in the pathogenesis of AD. MANF is expressed in neurons of the brain and spinal cord. However, there have been no investigations on MANF expression in the brain of AD patients. This was addressed in the present study by immunohistochemistry, western blotting, and quantitative analyses of postmortem brain specimens. We examined the localization and expression levels of MANF in the inferior temporal gyrus of the cortex (ITGC) in AD patients (n = 5), preclinical (pre-)AD patients (n = 5), and age-matched non-dementia controls (n = 5) by double immunofluorescence labeling with antibodies against the neuron-specific nuclear protein neuronal nuclei (NeuN), ER chaperone protein 78-kDa glucose-regulated protein (GRP78), and MANF. The results showed that MANF was mainly expressed in neurons of the ITGC in all 3 groups; However, the number of MANF-positive neurons was significantly higher in pre-AD (Braak stage III/IV) and AD (Braak stage V/VI) patients than that in the control group. Thus, MANF is overexpressed in AD and pre-AD, suggesting that it can serve as a diagnostic marker for early stage disease. Frontiers Media S.A. 2021-04-29 /pmc/articles/PMC8117094/ /pubmed/33994992 http://dx.doi.org/10.3389/fnagi.2021.639318 Text en Copyright © 2021 Liu, Qi, Fang, Zhou, Wang and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Liu, Xue-Chun Qi, Xiu-Hong Fang, Hui Zhou, Ke-Qing Wang, Qing-Song Chen, Gui-Hai Increased MANF Expression in the Inferior Temporal Gyrus in Patients With Alzheimer Disease |
title | Increased MANF Expression in the Inferior Temporal Gyrus in Patients With Alzheimer Disease |
title_full | Increased MANF Expression in the Inferior Temporal Gyrus in Patients With Alzheimer Disease |
title_fullStr | Increased MANF Expression in the Inferior Temporal Gyrus in Patients With Alzheimer Disease |
title_full_unstemmed | Increased MANF Expression in the Inferior Temporal Gyrus in Patients With Alzheimer Disease |
title_short | Increased MANF Expression in the Inferior Temporal Gyrus in Patients With Alzheimer Disease |
title_sort | increased manf expression in the inferior temporal gyrus in patients with alzheimer disease |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117094/ https://www.ncbi.nlm.nih.gov/pubmed/33994992 http://dx.doi.org/10.3389/fnagi.2021.639318 |
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