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Amyloid plaque formation precedes dendritic spine loss
Amyloid-beta plaque deposition represents a major neuropathological hallmark of Alzheimer’s disease. While numerous studies have described dendritic spine loss in proximity to plaques, much less is known about the kinetics of these processes. In particular, the question as to whether synapse loss pr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3508278/ https://www.ncbi.nlm.nih.gov/pubmed/22993126 http://dx.doi.org/10.1007/s00401-012-1047-8 |
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author | Bittner, Tobias Burgold, Steffen Dorostkar, Mario M. Fuhrmann, Martin Wegenast-Braun, Bettina M. Schmidt, Boris Kretzschmar, Hans Herms, Jochen |
author_facet | Bittner, Tobias Burgold, Steffen Dorostkar, Mario M. Fuhrmann, Martin Wegenast-Braun, Bettina M. Schmidt, Boris Kretzschmar, Hans Herms, Jochen |
author_sort | Bittner, Tobias |
collection | PubMed |
description | Amyloid-beta plaque deposition represents a major neuropathological hallmark of Alzheimer’s disease. While numerous studies have described dendritic spine loss in proximity to plaques, much less is known about the kinetics of these processes. In particular, the question as to whether synapse loss precedes or follows plaque formation remains unanswered. To address this question, and to learn more about the underlying kinetics, we simultaneously imaged amyloid plaque deposition and dendritic spine loss by applying two-photon in vivo microscopy through a cranial window in double transgenic APPPS1 mice. As a result, we first observed that the rate of dendritic spine loss in proximity to plaques is the same in both young and aged animals. However, plaque size only increased significantly in the young cohort, indicating that spine loss persists even many months after initial plaque appearance. Tracking the fate of individual spines revealed that net spine loss is caused by increased spine elimination, with the rate of spine formation remaining constant. Imaging of dendritic spines before and during plaque formation demonstrated that spine loss around plaques commences at least 4 weeks after initial plaque formation. In conclusion, spine loss occurs, shortly but with a significant time delay, after the birth of new plaques, and persists in the vicinity of amyloid plaques over many months. These findings hence give further hope to the possibility that there is a therapeutic window between initial amyloid plaque deposition and the onset of structural damage at spines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00401-012-1047-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3508278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-35082782012-11-28 Amyloid plaque formation precedes dendritic spine loss Bittner, Tobias Burgold, Steffen Dorostkar, Mario M. Fuhrmann, Martin Wegenast-Braun, Bettina M. Schmidt, Boris Kretzschmar, Hans Herms, Jochen Acta Neuropathol Original Paper Amyloid-beta plaque deposition represents a major neuropathological hallmark of Alzheimer’s disease. While numerous studies have described dendritic spine loss in proximity to plaques, much less is known about the kinetics of these processes. In particular, the question as to whether synapse loss precedes or follows plaque formation remains unanswered. To address this question, and to learn more about the underlying kinetics, we simultaneously imaged amyloid plaque deposition and dendritic spine loss by applying two-photon in vivo microscopy through a cranial window in double transgenic APPPS1 mice. As a result, we first observed that the rate of dendritic spine loss in proximity to plaques is the same in both young and aged animals. However, plaque size only increased significantly in the young cohort, indicating that spine loss persists even many months after initial plaque appearance. Tracking the fate of individual spines revealed that net spine loss is caused by increased spine elimination, with the rate of spine formation remaining constant. Imaging of dendritic spines before and during plaque formation demonstrated that spine loss around plaques commences at least 4 weeks after initial plaque formation. In conclusion, spine loss occurs, shortly but with a significant time delay, after the birth of new plaques, and persists in the vicinity of amyloid plaques over many months. These findings hence give further hope to the possibility that there is a therapeutic window between initial amyloid plaque deposition and the onset of structural damage at spines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00401-012-1047-8) contains supplementary material, which is available to authorized users. Springer-Verlag 2012-09-21 2012 /pmc/articles/PMC3508278/ /pubmed/22993126 http://dx.doi.org/10.1007/s00401-012-1047-8 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Paper Bittner, Tobias Burgold, Steffen Dorostkar, Mario M. Fuhrmann, Martin Wegenast-Braun, Bettina M. Schmidt, Boris Kretzschmar, Hans Herms, Jochen Amyloid plaque formation precedes dendritic spine loss |
title | Amyloid plaque formation precedes dendritic spine loss |
title_full | Amyloid plaque formation precedes dendritic spine loss |
title_fullStr | Amyloid plaque formation precedes dendritic spine loss |
title_full_unstemmed | Amyloid plaque formation precedes dendritic spine loss |
title_short | Amyloid plaque formation precedes dendritic spine loss |
title_sort | amyloid plaque formation precedes dendritic spine loss |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3508278/ https://www.ncbi.nlm.nih.gov/pubmed/22993126 http://dx.doi.org/10.1007/s00401-012-1047-8 |
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