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Cortical laminar tau deposits and activated astrocytes in Alzheimer’s disease visualised by (3)H-THK5117 and (3)H-deprenyl autoradiography
Hyperphosphorylated tau protein deposits and, inflammatory processes are characteristic components of Alzheimer disease (AD) pathology. We here aimed to visualize in vitro the distribution of tau deposits and activated astrocytes across the cortical layers in autopsy AD brain tissue using the radiot...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379625/ https://www.ncbi.nlm.nih.gov/pubmed/28374768 http://dx.doi.org/10.1038/srep45496 |
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author | Lemoine, Laetitia Saint-Aubert, Laure Nennesmo, Inger Gillberg, Per-Göran Nordberg, Agneta |
author_facet | Lemoine, Laetitia Saint-Aubert, Laure Nennesmo, Inger Gillberg, Per-Göran Nordberg, Agneta |
author_sort | Lemoine, Laetitia |
collection | PubMed |
description | Hyperphosphorylated tau protein deposits and, inflammatory processes are characteristic components of Alzheimer disease (AD) pathology. We here aimed to visualize in vitro the distribution of tau deposits and activated astrocytes across the cortical layers in autopsy AD brain tissue using the radiotracers (3)H-THK5117 and (3)H-deprenyl. (3)H-THK5117 and (3)H-deprenyl autoradiographies were carried out on frozen brain sections from three AD patients and one healthy control. (3)H-THK5117 showed a distinct laminar cortical binding similar to (3)H-deprenyl autoradiography, with an extensive binding in the superficial and deep layers of the temporal neocortices, whereas the middle frontal gyrus showed an even binding throughout the layers. Globally, eventhough some differences could be observed, AT8 (tau) and GFAP (astrocyte) immunostaining showed a laminar pattern comparable to their corresponding radiotracers within each AD case. Some variability was observed between the AD cases reflecting differences in disease phenotype. The similar laminar cortical brain distribution of tau deposits and activated astrocytes supports the hypothesis of a close pathological interconnection. The difference in regional binding patterns of (3)H-THK5117 and AT8 antibody staining suggest additional tau binding sites detectable by (3)H-THK5117. |
format | Online Article Text |
id | pubmed-5379625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53796252017-04-07 Cortical laminar tau deposits and activated astrocytes in Alzheimer’s disease visualised by (3)H-THK5117 and (3)H-deprenyl autoradiography Lemoine, Laetitia Saint-Aubert, Laure Nennesmo, Inger Gillberg, Per-Göran Nordberg, Agneta Sci Rep Article Hyperphosphorylated tau protein deposits and, inflammatory processes are characteristic components of Alzheimer disease (AD) pathology. We here aimed to visualize in vitro the distribution of tau deposits and activated astrocytes across the cortical layers in autopsy AD brain tissue using the radiotracers (3)H-THK5117 and (3)H-deprenyl. (3)H-THK5117 and (3)H-deprenyl autoradiographies were carried out on frozen brain sections from three AD patients and one healthy control. (3)H-THK5117 showed a distinct laminar cortical binding similar to (3)H-deprenyl autoradiography, with an extensive binding in the superficial and deep layers of the temporal neocortices, whereas the middle frontal gyrus showed an even binding throughout the layers. Globally, eventhough some differences could be observed, AT8 (tau) and GFAP (astrocyte) immunostaining showed a laminar pattern comparable to their corresponding radiotracers within each AD case. Some variability was observed between the AD cases reflecting differences in disease phenotype. The similar laminar cortical brain distribution of tau deposits and activated astrocytes supports the hypothesis of a close pathological interconnection. The difference in regional binding patterns of (3)H-THK5117 and AT8 antibody staining suggest additional tau binding sites detectable by (3)H-THK5117. Nature Publishing Group 2017-04-04 /pmc/articles/PMC5379625/ /pubmed/28374768 http://dx.doi.org/10.1038/srep45496 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lemoine, Laetitia Saint-Aubert, Laure Nennesmo, Inger Gillberg, Per-Göran Nordberg, Agneta Cortical laminar tau deposits and activated astrocytes in Alzheimer’s disease visualised by (3)H-THK5117 and (3)H-deprenyl autoradiography |
title | Cortical laminar tau deposits and activated astrocytes in Alzheimer’s disease visualised by (3)H-THK5117 and (3)H-deprenyl autoradiography |
title_full | Cortical laminar tau deposits and activated astrocytes in Alzheimer’s disease visualised by (3)H-THK5117 and (3)H-deprenyl autoradiography |
title_fullStr | Cortical laminar tau deposits and activated astrocytes in Alzheimer’s disease visualised by (3)H-THK5117 and (3)H-deprenyl autoradiography |
title_full_unstemmed | Cortical laminar tau deposits and activated astrocytes in Alzheimer’s disease visualised by (3)H-THK5117 and (3)H-deprenyl autoradiography |
title_short | Cortical laminar tau deposits and activated astrocytes in Alzheimer’s disease visualised by (3)H-THK5117 and (3)H-deprenyl autoradiography |
title_sort | cortical laminar tau deposits and activated astrocytes in alzheimer’s disease visualised by (3)h-thk5117 and (3)h-deprenyl autoradiography |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379625/ https://www.ncbi.nlm.nih.gov/pubmed/28374768 http://dx.doi.org/10.1038/srep45496 |
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