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C5aR1 signaling promotes region and age dependent synaptic pruning in models of Alzheimer’s Disease
INTRODUCTION: Synaptic loss is a hallmark of Alzheimer’s disease (AD) that correlates with cognitive decline in AD patients. Complement-mediated synaptic pruning has been associated with this excessive loss of synapses in AD. Here, we investigated the effect of C5aR1 inhibition on microglial and ast...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592845/ https://www.ncbi.nlm.nih.gov/pubmed/37873302 http://dx.doi.org/10.1101/2023.09.29.560234 |
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author | Gomez-Arboledas, Angela Fonseca, Maria I. Kramar, Enikö Chu, Shu-Hui Schartz, Nicole Selvan, Purnika Wood, Marcelo A. Tenner, Andrea J. |
author_facet | Gomez-Arboledas, Angela Fonseca, Maria I. Kramar, Enikö Chu, Shu-Hui Schartz, Nicole Selvan, Purnika Wood, Marcelo A. Tenner, Andrea J. |
author_sort | Gomez-Arboledas, Angela |
collection | PubMed |
description | INTRODUCTION: Synaptic loss is a hallmark of Alzheimer’s disease (AD) that correlates with cognitive decline in AD patients. Complement-mediated synaptic pruning has been associated with this excessive loss of synapses in AD. Here, we investigated the effect of C5aR1 inhibition on microglial and astroglial synaptic pruning in two mouse models of AD. METHODS: A combination of super-resolution and confocal and tridimensional image reconstruction was used to assess the effect of genetic ablation or pharmacological inhibition of C5aR1 on the Arctic48 and Tg2576 models of AD. RESULTS: Genetic ablation or pharmacological inhibition of C5aR1 rescues the excessive pre-synaptic pruning and synaptic loss in an age and region dependent fashion in two mouse models of AD, which correlates with improved long-term potentiation (LTP). DISCUSSION: Reduction of excessive synaptic pruning is an additional beneficial outcome of the suppression of C5a-C5aR1 signaling, further supporting its potential as an effective targeted therapy to treat AD. |
format | Online Article Text |
id | pubmed-10592845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105928452023-10-24 C5aR1 signaling promotes region and age dependent synaptic pruning in models of Alzheimer’s Disease Gomez-Arboledas, Angela Fonseca, Maria I. Kramar, Enikö Chu, Shu-Hui Schartz, Nicole Selvan, Purnika Wood, Marcelo A. Tenner, Andrea J. bioRxiv Article INTRODUCTION: Synaptic loss is a hallmark of Alzheimer’s disease (AD) that correlates with cognitive decline in AD patients. Complement-mediated synaptic pruning has been associated with this excessive loss of synapses in AD. Here, we investigated the effect of C5aR1 inhibition on microglial and astroglial synaptic pruning in two mouse models of AD. METHODS: A combination of super-resolution and confocal and tridimensional image reconstruction was used to assess the effect of genetic ablation or pharmacological inhibition of C5aR1 on the Arctic48 and Tg2576 models of AD. RESULTS: Genetic ablation or pharmacological inhibition of C5aR1 rescues the excessive pre-synaptic pruning and synaptic loss in an age and region dependent fashion in two mouse models of AD, which correlates with improved long-term potentiation (LTP). DISCUSSION: Reduction of excessive synaptic pruning is an additional beneficial outcome of the suppression of C5a-C5aR1 signaling, further supporting its potential as an effective targeted therapy to treat AD. Cold Spring Harbor Laboratory 2023-10-02 /pmc/articles/PMC10592845/ /pubmed/37873302 http://dx.doi.org/10.1101/2023.09.29.560234 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Gomez-Arboledas, Angela Fonseca, Maria I. Kramar, Enikö Chu, Shu-Hui Schartz, Nicole Selvan, Purnika Wood, Marcelo A. Tenner, Andrea J. C5aR1 signaling promotes region and age dependent synaptic pruning in models of Alzheimer’s Disease |
title | C5aR1 signaling promotes region and age dependent synaptic pruning in models of Alzheimer’s Disease |
title_full | C5aR1 signaling promotes region and age dependent synaptic pruning in models of Alzheimer’s Disease |
title_fullStr | C5aR1 signaling promotes region and age dependent synaptic pruning in models of Alzheimer’s Disease |
title_full_unstemmed | C5aR1 signaling promotes region and age dependent synaptic pruning in models of Alzheimer’s Disease |
title_short | C5aR1 signaling promotes region and age dependent synaptic pruning in models of Alzheimer’s Disease |
title_sort | c5ar1 signaling promotes region and age dependent synaptic pruning in models of alzheimer’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592845/ https://www.ncbi.nlm.nih.gov/pubmed/37873302 http://dx.doi.org/10.1101/2023.09.29.560234 |
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