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Phosphorylation Signaling in APP Processing in Alzheimer’s Disease

The abnormal accumulation of amyloid-β (Aβ) in the central nervous system is a hallmark of Alzheimer’s disease (AD). The regulation of the processing of the single- transmembrane amyloid precursor protein (APP) plays an important role in the generation of Aβ in the brain. The phosphorylation of APP...

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Detalles Bibliográficos
Autores principales: Zhang, Tao, Chen, Dongmei, Lee, Tae Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981488/
https://www.ncbi.nlm.nih.gov/pubmed/31892243
http://dx.doi.org/10.3390/ijms21010209
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author Zhang, Tao
Chen, Dongmei
Lee, Tae Ho
author_facet Zhang, Tao
Chen, Dongmei
Lee, Tae Ho
author_sort Zhang, Tao
collection PubMed
description The abnormal accumulation of amyloid-β (Aβ) in the central nervous system is a hallmark of Alzheimer’s disease (AD). The regulation of the processing of the single- transmembrane amyloid precursor protein (APP) plays an important role in the generation of Aβ in the brain. The phosphorylation of APP and key enzymes involved in the proteolytic processing of APP has been demonstrated to be critical for modulating the generation of Aβ by either altering the subcellular localization of APP or changing the enzymatic activities of the secretases responsible for APP processing. In addition, the phosphorylation may also have an impact on the physiological function of these proteins. In this review, we summarize the kinases and signaling pathways that may participate in regulating the phosphorylation of APP and secretases and how this further affects the function and processing of APP and Aβ pathology. We also discuss the potential of approaches that modulate these phosphorylation-signaling pathways or kinases as interventions for AD pathology.
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spelling pubmed-69814882020-02-07 Phosphorylation Signaling in APP Processing in Alzheimer’s Disease Zhang, Tao Chen, Dongmei Lee, Tae Ho Int J Mol Sci Review The abnormal accumulation of amyloid-β (Aβ) in the central nervous system is a hallmark of Alzheimer’s disease (AD). The regulation of the processing of the single- transmembrane amyloid precursor protein (APP) plays an important role in the generation of Aβ in the brain. The phosphorylation of APP and key enzymes involved in the proteolytic processing of APP has been demonstrated to be critical for modulating the generation of Aβ by either altering the subcellular localization of APP or changing the enzymatic activities of the secretases responsible for APP processing. In addition, the phosphorylation may also have an impact on the physiological function of these proteins. In this review, we summarize the kinases and signaling pathways that may participate in regulating the phosphorylation of APP and secretases and how this further affects the function and processing of APP and Aβ pathology. We also discuss the potential of approaches that modulate these phosphorylation-signaling pathways or kinases as interventions for AD pathology. MDPI 2019-12-27 /pmc/articles/PMC6981488/ /pubmed/31892243 http://dx.doi.org/10.3390/ijms21010209 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zhang, Tao
Chen, Dongmei
Lee, Tae Ho
Phosphorylation Signaling in APP Processing in Alzheimer’s Disease
title Phosphorylation Signaling in APP Processing in Alzheimer’s Disease
title_full Phosphorylation Signaling in APP Processing in Alzheimer’s Disease
title_fullStr Phosphorylation Signaling in APP Processing in Alzheimer’s Disease
title_full_unstemmed Phosphorylation Signaling in APP Processing in Alzheimer’s Disease
title_short Phosphorylation Signaling in APP Processing in Alzheimer’s Disease
title_sort phosphorylation signaling in app processing in alzheimer’s disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981488/
https://www.ncbi.nlm.nih.gov/pubmed/31892243
http://dx.doi.org/10.3390/ijms21010209
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