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The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease
In the majority of affected brain regions the pathological hallmarks of Alzheimer’s disease (AD) are β-amyloid (Aβ) deposits in the form of diffuse and neuritic plaques, tau pathology in the form of neurofibrillary tangles, neuropil threads and plaque-associated abnormal neurites in combination with...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053705/ https://www.ncbi.nlm.nih.gov/pubmed/30029687 http://dx.doi.org/10.1186/s40478-018-0563-8 |
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author | Murray, Christina E. Gami-Patel, Priya Gkanatsiou, Eleni Brinkmalm, Gunnar Portelius, Erik Wirths, Oliver Heywood, Wendy Blennow, Kaj Ghiso, Jorge Holton, Janice L. Mills, Kevin Zetterberg, Henrik Revesz, Tamas Lashley, Tammaryn |
author_facet | Murray, Christina E. Gami-Patel, Priya Gkanatsiou, Eleni Brinkmalm, Gunnar Portelius, Erik Wirths, Oliver Heywood, Wendy Blennow, Kaj Ghiso, Jorge Holton, Janice L. Mills, Kevin Zetterberg, Henrik Revesz, Tamas Lashley, Tammaryn |
author_sort | Murray, Christina E. |
collection | PubMed |
description | In the majority of affected brain regions the pathological hallmarks of Alzheimer’s disease (AD) are β-amyloid (Aβ) deposits in the form of diffuse and neuritic plaques, tau pathology in the form of neurofibrillary tangles, neuropil threads and plaque-associated abnormal neurites in combination with an inflammatory response. However, the anatomical area of the presubiculum, is characterised by the presence of a single large evenly distributed ‘lake-like’ Aβ deposit with minimal tau deposition or accumulation of inflammatory markers. Post-mortem brain samples from sporadic AD (SAD) and familial AD (FAD) and two hereditary cerebral amyloid diseases, familial British dementia (FBD) and familial Danish dementia (FDD) were used to compare the morphology of the extracellular proteins deposited in the presubiculum compared to the entorhinal cortex. The level of tau pathology and the extent of microglial activation were quantitated in the two brain regions in SAD and FAD. Frozen tissue was used to investigate the Aβ species and proteomic differences between the two regions. Consistent with our previous investigations of FBD and FDD cases we were able to establish that the ‘lake-like’ pre-amyloid deposits of the presubiculum were not a unique feature of AD but they also found two non-Aβ amyloidosis. Comparing the presubiculum to the entorhinal cortex the number of neurofibrillary tangles and tau load were significantly reduced; there was a reduction in microglial activation; there were differences in the Aβ profiles and the investigation of the whole proteome showed significant changes in different protein pathways. In summary, understanding why the presubiculum has a different morphological appearance, biochemical and proteomic makeup compared to surrounding brain regions severely affected by neurodegeneration could lead us to understanding protective mechanisms in neurodegenerative diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-018-0563-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6053705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60537052018-07-23 The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease Murray, Christina E. Gami-Patel, Priya Gkanatsiou, Eleni Brinkmalm, Gunnar Portelius, Erik Wirths, Oliver Heywood, Wendy Blennow, Kaj Ghiso, Jorge Holton, Janice L. Mills, Kevin Zetterberg, Henrik Revesz, Tamas Lashley, Tammaryn Acta Neuropathol Commun Research In the majority of affected brain regions the pathological hallmarks of Alzheimer’s disease (AD) are β-amyloid (Aβ) deposits in the form of diffuse and neuritic plaques, tau pathology in the form of neurofibrillary tangles, neuropil threads and plaque-associated abnormal neurites in combination with an inflammatory response. However, the anatomical area of the presubiculum, is characterised by the presence of a single large evenly distributed ‘lake-like’ Aβ deposit with minimal tau deposition or accumulation of inflammatory markers. Post-mortem brain samples from sporadic AD (SAD) and familial AD (FAD) and two hereditary cerebral amyloid diseases, familial British dementia (FBD) and familial Danish dementia (FDD) were used to compare the morphology of the extracellular proteins deposited in the presubiculum compared to the entorhinal cortex. The level of tau pathology and the extent of microglial activation were quantitated in the two brain regions in SAD and FAD. Frozen tissue was used to investigate the Aβ species and proteomic differences between the two regions. Consistent with our previous investigations of FBD and FDD cases we were able to establish that the ‘lake-like’ pre-amyloid deposits of the presubiculum were not a unique feature of AD but they also found two non-Aβ amyloidosis. Comparing the presubiculum to the entorhinal cortex the number of neurofibrillary tangles and tau load were significantly reduced; there was a reduction in microglial activation; there were differences in the Aβ profiles and the investigation of the whole proteome showed significant changes in different protein pathways. In summary, understanding why the presubiculum has a different morphological appearance, biochemical and proteomic makeup compared to surrounding brain regions severely affected by neurodegeneration could lead us to understanding protective mechanisms in neurodegenerative diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-018-0563-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-20 /pmc/articles/PMC6053705/ /pubmed/30029687 http://dx.doi.org/10.1186/s40478-018-0563-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Murray, Christina E. Gami-Patel, Priya Gkanatsiou, Eleni Brinkmalm, Gunnar Portelius, Erik Wirths, Oliver Heywood, Wendy Blennow, Kaj Ghiso, Jorge Holton, Janice L. Mills, Kevin Zetterberg, Henrik Revesz, Tamas Lashley, Tammaryn The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease |
title | The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease |
title_full | The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease |
title_fullStr | The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease |
title_full_unstemmed | The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease |
title_short | The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease |
title_sort | presubiculum is preserved from neurodegenerative changes in alzheimer’s disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053705/ https://www.ncbi.nlm.nih.gov/pubmed/30029687 http://dx.doi.org/10.1186/s40478-018-0563-8 |
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