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A Neuron-Glial Model of Exosomal Release in the Onset and Progression of Alzheimer's Disease

Exosomes are nano-sized extracellular vesicles that perform a variety of biological functions linked to the pathogenesis of various neurodegenerative disorders. In Alzheimer's disease (AD), for examples, exosomes are responsible for the release of Aβ oligomers, and their extracellular accumulat...

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Autores principales: Shaheen, Hina, Singh, Sundeep, Melnik, Roderick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489198/
https://www.ncbi.nlm.nih.gov/pubmed/34616283
http://dx.doi.org/10.3389/fncom.2021.653097
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author Shaheen, Hina
Singh, Sundeep
Melnik, Roderick
author_facet Shaheen, Hina
Singh, Sundeep
Melnik, Roderick
author_sort Shaheen, Hina
collection PubMed
description Exosomes are nano-sized extracellular vesicles that perform a variety of biological functions linked to the pathogenesis of various neurodegenerative disorders. In Alzheimer's disease (AD), for examples, exosomes are responsible for the release of Aβ oligomers, and their extracellular accumulation, although the underpinning molecular machinery remains elusive. We propose a novel model for Alzheimer's Aβ accumulation based on Ca(2+)-dependent exosome release from astrocytes. Moreover, we exploit our model to assess how temperature dependence of exosome release could interact with Aβ neurotoxicity. We predict that voltage-gated Ca(2+) channels (VGCCs) along with the transient-receptor potential M8 (TRPM8) channel are crucial molecular components in Alzheimer's progression.
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spelling pubmed-84891982021-10-05 A Neuron-Glial Model of Exosomal Release in the Onset and Progression of Alzheimer's Disease Shaheen, Hina Singh, Sundeep Melnik, Roderick Front Comput Neurosci Neuroscience Exosomes are nano-sized extracellular vesicles that perform a variety of biological functions linked to the pathogenesis of various neurodegenerative disorders. In Alzheimer's disease (AD), for examples, exosomes are responsible for the release of Aβ oligomers, and their extracellular accumulation, although the underpinning molecular machinery remains elusive. We propose a novel model for Alzheimer's Aβ accumulation based on Ca(2+)-dependent exosome release from astrocytes. Moreover, we exploit our model to assess how temperature dependence of exosome release could interact with Aβ neurotoxicity. We predict that voltage-gated Ca(2+) channels (VGCCs) along with the transient-receptor potential M8 (TRPM8) channel are crucial molecular components in Alzheimer's progression. Frontiers Media S.A. 2021-09-20 /pmc/articles/PMC8489198/ /pubmed/34616283 http://dx.doi.org/10.3389/fncom.2021.653097 Text en Copyright © 2021 Shaheen, Singh and Melnik. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Shaheen, Hina
Singh, Sundeep
Melnik, Roderick
A Neuron-Glial Model of Exosomal Release in the Onset and Progression of Alzheimer's Disease
title A Neuron-Glial Model of Exosomal Release in the Onset and Progression of Alzheimer's Disease
title_full A Neuron-Glial Model of Exosomal Release in the Onset and Progression of Alzheimer's Disease
title_fullStr A Neuron-Glial Model of Exosomal Release in the Onset and Progression of Alzheimer's Disease
title_full_unstemmed A Neuron-Glial Model of Exosomal Release in the Onset and Progression of Alzheimer's Disease
title_short A Neuron-Glial Model of Exosomal Release in the Onset and Progression of Alzheimer's Disease
title_sort neuron-glial model of exosomal release in the onset and progression of alzheimer's disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489198/
https://www.ncbi.nlm.nih.gov/pubmed/34616283
http://dx.doi.org/10.3389/fncom.2021.653097
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