Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Gomez-Arboledas, Angela, Fonseca, Maria I., Kramar, Enikö, Chu, Shu-Hui, Schartz, Nicole, Selvan, Purnika, Wood, Marcelo A., Tenner, Andrea J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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
_version_ 1785124352691273728
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
work_keys_str_mv AT gomezarboledasangela c5ar1signalingpromotesregionandagedependentsynapticpruninginmodelsofalzheimersdisease
AT fonsecamariai c5ar1signalingpromotesregionandagedependentsynapticpruninginmodelsofalzheimersdisease
AT kramareniko c5ar1signalingpromotesregionandagedependentsynapticpruninginmodelsofalzheimersdisease
AT chushuhui c5ar1signalingpromotesregionandagedependentsynapticpruninginmodelsofalzheimersdisease
AT schartznicole c5ar1signalingpromotesregionandagedependentsynapticpruninginmodelsofalzheimersdisease
AT selvanpurnika c5ar1signalingpromotesregionandagedependentsynapticpruninginmodelsofalzheimersdisease
AT woodmarceloa c5ar1signalingpromotesregionandagedependentsynapticpruninginmodelsofalzheimersdisease
AT tennerandreaj c5ar1signalingpromotesregionandagedependentsynapticpruninginmodelsofalzheimersdisease