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Plasmalogens Inhibit APP Processing by Directly Affecting γ-Secretase Activity in Alzheimer's Disease
Lipids play an important role as risk or protective factors in Alzheimer's disease (AD). Previously it has been shown that plasmalogens, the major brain phospholipids, are altered in AD. However, it remained unclear whether plasmalogens themselves are able to modulate amyloid precursor protein...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Scientific World Journal
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322458/ https://www.ncbi.nlm.nih.gov/pubmed/22547976 http://dx.doi.org/10.1100/2012/141240 |
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author | Rothhaar, Tatjana L. Grösgen, Sven Haupenthal, Viola J. Burg, Verena K. Hundsdörfer, Benjamin Mett, Janine Riemenschneider, Matthias Grimm, Heike S. Hartmann, Tobias Grimm, Marcus O. W. |
author_facet | Rothhaar, Tatjana L. Grösgen, Sven Haupenthal, Viola J. Burg, Verena K. Hundsdörfer, Benjamin Mett, Janine Riemenschneider, Matthias Grimm, Heike S. Hartmann, Tobias Grimm, Marcus O. W. |
author_sort | Rothhaar, Tatjana L. |
collection | PubMed |
description | Lipids play an important role as risk or protective factors in Alzheimer's disease (AD). Previously it has been shown that plasmalogens, the major brain phospholipids, are altered in AD. However, it remained unclear whether plasmalogens themselves are able to modulate amyloid precursor protein (APP) processing or if the reduced plasmalogen level is a consequence of AD. Here we identify the plasmalogens which are altered in human AD postmortem brains and investigate their impact on APP processing resulting in Aβ production. All tested plasmalogen species showed a reduction in γ-secretase activity whereas β- and α-secretase activity mainly remained unchanged. Plasmalogens directly affected γ-secretase activity, protein and RNA level of the secretases were unaffected, pointing towards a direct influence of plasmalogens on γ-secretase activity. Plasmalogens were also able to decrease γ-secretase activity in human postmortem AD brains emphasizing the impact of plasmalogens in AD. In summary our findings show that decreased plasmalogen levels are not only a consequence of AD but that plasmalogens also decrease APP processing by directly affecting γ-secretase activity, resulting in a vicious cycle: Aβ reduces plasmalogen levels and reduced plasmalogen levels directly increase γ-secretase activity leading to an even stronger production of Aβ peptides. |
format | Online Article Text |
id | pubmed-3322458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Scientific World Journal |
record_format | MEDLINE/PubMed |
spelling | pubmed-33224582012-04-30 Plasmalogens Inhibit APP Processing by Directly Affecting γ-Secretase Activity in Alzheimer's Disease Rothhaar, Tatjana L. Grösgen, Sven Haupenthal, Viola J. Burg, Verena K. Hundsdörfer, Benjamin Mett, Janine Riemenschneider, Matthias Grimm, Heike S. Hartmann, Tobias Grimm, Marcus O. W. ScientificWorldJournal Research Article Lipids play an important role as risk or protective factors in Alzheimer's disease (AD). Previously it has been shown that plasmalogens, the major brain phospholipids, are altered in AD. However, it remained unclear whether plasmalogens themselves are able to modulate amyloid precursor protein (APP) processing or if the reduced plasmalogen level is a consequence of AD. Here we identify the plasmalogens which are altered in human AD postmortem brains and investigate their impact on APP processing resulting in Aβ production. All tested plasmalogen species showed a reduction in γ-secretase activity whereas β- and α-secretase activity mainly remained unchanged. Plasmalogens directly affected γ-secretase activity, protein and RNA level of the secretases were unaffected, pointing towards a direct influence of plasmalogens on γ-secretase activity. Plasmalogens were also able to decrease γ-secretase activity in human postmortem AD brains emphasizing the impact of plasmalogens in AD. In summary our findings show that decreased plasmalogen levels are not only a consequence of AD but that plasmalogens also decrease APP processing by directly affecting γ-secretase activity, resulting in a vicious cycle: Aβ reduces plasmalogen levels and reduced plasmalogen levels directly increase γ-secretase activity leading to an even stronger production of Aβ peptides. The Scientific World Journal 2012-04-01 /pmc/articles/PMC3322458/ /pubmed/22547976 http://dx.doi.org/10.1100/2012/141240 Text en Copyright © 2012 Tatjana L. Rothhaar et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Rothhaar, Tatjana L. Grösgen, Sven Haupenthal, Viola J. Burg, Verena K. Hundsdörfer, Benjamin Mett, Janine Riemenschneider, Matthias Grimm, Heike S. Hartmann, Tobias Grimm, Marcus O. W. Plasmalogens Inhibit APP Processing by Directly Affecting γ-Secretase Activity in Alzheimer's Disease |
title | Plasmalogens Inhibit APP Processing by Directly Affecting γ-Secretase Activity in Alzheimer's Disease |
title_full | Plasmalogens Inhibit APP Processing by Directly Affecting γ-Secretase Activity in Alzheimer's Disease |
title_fullStr | Plasmalogens Inhibit APP Processing by Directly Affecting γ-Secretase Activity in Alzheimer's Disease |
title_full_unstemmed | Plasmalogens Inhibit APP Processing by Directly Affecting γ-Secretase Activity in Alzheimer's Disease |
title_short | Plasmalogens Inhibit APP Processing by Directly Affecting γ-Secretase Activity in Alzheimer's Disease |
title_sort | plasmalogens inhibit app processing by directly affecting γ-secretase activity in alzheimer's disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322458/ https://www.ncbi.nlm.nih.gov/pubmed/22547976 http://dx.doi.org/10.1100/2012/141240 |
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