Amyloid precursor protein maintains constitutive and adaptive plasticity of dendritic spines in adult brain by regulating D-serine homeostasis

Dynamic synapses facilitate activity-dependent remodeling of neural circuits, thereby providing the structural substrate for adaptive behaviors. However, the mechanisms governing dynamic synapses in adult brain are still largely unknown. Here, we demonstrate that in the cortex of adult amyloid precu...

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Bibliographic Details
Main Authors: Zou, Chengyu (Author) , Müller, Ulrike C. (Author)
Format: Article (Journal)
Language:English
Published: 17 October 2016
In: The EMBO journal
Year: 2016, Volume: 35, Issue: 20, Pages: 2213-2222
ISSN:1460-2075
DOI:10.15252/embj.201694085
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.15252/embj.201694085
Verlag, lizenzpflichtig, Volltext: https://www.embopress.org/doi/full/10.15252/embj.201694085
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Author Notes:Chengyu Zou, Sophie Crux, Stephane Marinesco, Elena Montagna, Carmelo Sgobio, Yuan Shi, Song Shi, Kaichuan Zhu, Mario M. Dorostkar, Ulrike C. Müller & Jochen Herms
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Summary:Dynamic synapses facilitate activity-dependent remodeling of neural circuits, thereby providing the structural substrate for adaptive behaviors. However, the mechanisms governing dynamic synapses in adult brain are still largely unknown. Here, we demonstrate that in the cortex of adult amyloid precursor protein knockout (APP-KO) mice, spine formation and elimination were both reduced while overall spine density remained unaltered. When housed under environmental enrichment, APP-KO mice failed to respond with an increase in spine density. Spine morphology was also altered in the absence of APP. The underlying mechanism of these spine abnormalities in APP-KO mice was ascribed to an impairment in D-serine homeostasis. Extracellular D-serine concentration was significantly reduced in APP-KO mice, coupled with an increase of total D-serine. Strikingly, chronic treatment with exogenous D-serine normalized D-serine homeostasis and restored the deficits of spine dynamics, adaptive plasticity, and morphology in APP-KO mice. The cognitive deficit observed in APP-KO mice was also rescued by D-serine treatment. These data suggest that APP regulates homeostasis of D-serine, thereby maintaining the constitutive and adaptive plasticity of dendritic spines in adult brain.
Item Description:Gesehen am 12.10.2021
Physical Description:Online Resource
ISSN:1460-2075
DOI:10.15252/embj.201694085