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Synaptic Cell Adhesion Molecules in Alzheimer's Disease

Alzheimer's disease (AD) is a neurodegenerative brain disorder associated with the loss of synapses between neurons in the brain. Synaptic cell adhesion molecules are cell surface glycoproteins which are expressed at the synaptic plasma membranes of neurons. These proteins play key roles in for...

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Autores principales: Leshchyns'ka, Iryna, Sytnyk, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868906/
https://www.ncbi.nlm.nih.gov/pubmed/27242933
http://dx.doi.org/10.1155/2016/6427537
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author Leshchyns'ka, Iryna
Sytnyk, Vladimir
author_facet Leshchyns'ka, Iryna
Sytnyk, Vladimir
author_sort Leshchyns'ka, Iryna
collection PubMed
description Alzheimer's disease (AD) is a neurodegenerative brain disorder associated with the loss of synapses between neurons in the brain. Synaptic cell adhesion molecules are cell surface glycoproteins which are expressed at the synaptic plasma membranes of neurons. These proteins play key roles in formation and maintenance of synapses and regulation of synaptic plasticity. Genetic studies and biochemical analysis of the human brain tissue, cerebrospinal fluid, and sera from AD patients indicate that levels and function of synaptic cell adhesion molecules are affected in AD. Synaptic cell adhesion molecules interact with Aβ, a peptide accumulating in AD brains, which affects their expression and synaptic localization. Synaptic cell adhesion molecules also regulate the production of Aβ via interaction with the key enzymes involved in Aβ formation. Aβ-dependent changes in synaptic adhesion affect the function and integrity of synapses suggesting that alterations in synaptic adhesion play key roles in the disruption of neuronal networks in AD.
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spelling pubmed-48689062016-05-30 Synaptic Cell Adhesion Molecules in Alzheimer's Disease Leshchyns'ka, Iryna Sytnyk, Vladimir Neural Plast Review Article Alzheimer's disease (AD) is a neurodegenerative brain disorder associated with the loss of synapses between neurons in the brain. Synaptic cell adhesion molecules are cell surface glycoproteins which are expressed at the synaptic plasma membranes of neurons. These proteins play key roles in formation and maintenance of synapses and regulation of synaptic plasticity. Genetic studies and biochemical analysis of the human brain tissue, cerebrospinal fluid, and sera from AD patients indicate that levels and function of synaptic cell adhesion molecules are affected in AD. Synaptic cell adhesion molecules interact with Aβ, a peptide accumulating in AD brains, which affects their expression and synaptic localization. Synaptic cell adhesion molecules also regulate the production of Aβ via interaction with the key enzymes involved in Aβ formation. Aβ-dependent changes in synaptic adhesion affect the function and integrity of synapses suggesting that alterations in synaptic adhesion play key roles in the disruption of neuronal networks in AD. Hindawi Publishing Corporation 2016 2016-05-03 /pmc/articles/PMC4868906/ /pubmed/27242933 http://dx.doi.org/10.1155/2016/6427537 Text en Copyright © 2016 I. Leshchyns'ka and V. Sytnyk. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Leshchyns'ka, Iryna
Sytnyk, Vladimir
Synaptic Cell Adhesion Molecules in Alzheimer's Disease
title Synaptic Cell Adhesion Molecules in Alzheimer's Disease
title_full Synaptic Cell Adhesion Molecules in Alzheimer's Disease
title_fullStr Synaptic Cell Adhesion Molecules in Alzheimer's Disease
title_full_unstemmed Synaptic Cell Adhesion Molecules in Alzheimer's Disease
title_short Synaptic Cell Adhesion Molecules in Alzheimer's Disease
title_sort synaptic cell adhesion molecules in alzheimer's disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868906/
https://www.ncbi.nlm.nih.gov/pubmed/27242933
http://dx.doi.org/10.1155/2016/6427537
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