The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease
Abstract 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 combina...
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doaj-d6defc590b0c4d959311b9d932f3cecd2020-11-25T01:11:46ZengBMCActa Neuropathologica Communications2051-59602018-07-016111710.1186/s40478-018-0563-8The presubiculum is preserved from neurodegenerative changes in Alzheimer’s diseaseChristina E. Murray0Priya Gami-Patel1Eleni Gkanatsiou2Gunnar Brinkmalm3Erik Portelius4Oliver Wirths5Wendy Heywood6Kaj Blennow7Jorge Ghiso8Janice L. Holton9Kevin Mills10Henrik Zetterberg11Tamas Revesz12Tammaryn Lashley13The Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of NeurologyThe Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of NeurologyInstitute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of GothenburgInstitute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of GothenburgInstitute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of GothenburgDepartment of Psychiatry and Psychotherapy, University Medical Center (UMG), Georg-August-UniversityCentre for Translational Omics, Great Ormond Street Institute of Child health, UCLInstitute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of GothenburgNew York UniversityThe Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of NeurologyCentre for Translational Omics, Great Ormond Street Institute of Child health, UCLInstitute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of GothenburgThe Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of NeurologyThe Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of NeurologyAbstract 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.http://link.springer.com/article/10.1186/s40478-018-0563-8Alzheimer’s diseasePresubiculumAmyloidTauNeuroinflammation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Christina E. Murray Priya Gami-Patel Eleni Gkanatsiou Gunnar Brinkmalm Erik Portelius Oliver Wirths Wendy Heywood Kaj Blennow Jorge Ghiso Janice L. Holton Kevin Mills Henrik Zetterberg Tamas Revesz Tammaryn Lashley |
spellingShingle |
Christina E. Murray Priya Gami-Patel Eleni Gkanatsiou Gunnar Brinkmalm Erik Portelius Oliver Wirths Wendy Heywood Kaj Blennow Jorge Ghiso Janice L. Holton Kevin Mills Henrik Zetterberg Tamas Revesz Tammaryn Lashley The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease Acta Neuropathologica Communications Alzheimer’s disease Presubiculum Amyloid Tau Neuroinflammation |
author_facet |
Christina E. Murray Priya Gami-Patel Eleni Gkanatsiou Gunnar Brinkmalm Erik Portelius Oliver Wirths Wendy Heywood Kaj Blennow Jorge Ghiso Janice L. Holton Kevin Mills Henrik Zetterberg Tamas Revesz Tammaryn Lashley |
author_sort |
Christina E. Murray |
title |
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_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_sort |
presubiculum is preserved from neurodegenerative changes in alzheimer’s disease |
publisher |
BMC |
series |
Acta Neuropathologica Communications |
issn |
2051-5960 |
publishDate |
2018-07-01 |
description |
Abstract 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. |
topic |
Alzheimer’s disease Presubiculum Amyloid Tau Neuroinflammation |
url |
http://link.springer.com/article/10.1186/s40478-018-0563-8 |
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