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α-Synuclein and Noradrenergic Modulation of Immune Cells in Parkinson’s Disease Pathogenesis

α-synuclein (α-syn) pathology and loss of noradrenergic neurons in the locus coeruleus (LC) are among the most ubiquitous features of Parkinson’s disease (PD). While noradrenergic dysfunction is associated with non-motor symptoms of PD, preclinical research suggests that the loss of LC norepinephrin...

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Autores principales: Butkovich, Laura M., Houser, Madelyn C., Tansey, Malú G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143806/
https://www.ncbi.nlm.nih.gov/pubmed/30258347
http://dx.doi.org/10.3389/fnins.2018.00626
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author Butkovich, Laura M.
Houser, Madelyn C.
Tansey, Malú G.
author_facet Butkovich, Laura M.
Houser, Madelyn C.
Tansey, Malú G.
author_sort Butkovich, Laura M.
collection PubMed
description α-synuclein (α-syn) pathology and loss of noradrenergic neurons in the locus coeruleus (LC) are among the most ubiquitous features of Parkinson’s disease (PD). While noradrenergic dysfunction is associated with non-motor symptoms of PD, preclinical research suggests that the loss of LC norepinephrine (NE), and subsequently its immune modulatory and neuroprotective actions, may exacerbate or even accelerate disease progression. In this review, we discuss the mechanisms by which α-syn pathology and loss of central NE may directly impact brain health by interrupting neurotrophic factor signaling, exacerbating neuroinflammation, and altering regulation of innate and adaptive immune cells.
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spelling pubmed-61438062018-09-26 α-Synuclein and Noradrenergic Modulation of Immune Cells in Parkinson’s Disease Pathogenesis Butkovich, Laura M. Houser, Madelyn C. Tansey, Malú G. Front Neurosci Neuroscience α-synuclein (α-syn) pathology and loss of noradrenergic neurons in the locus coeruleus (LC) are among the most ubiquitous features of Parkinson’s disease (PD). While noradrenergic dysfunction is associated with non-motor symptoms of PD, preclinical research suggests that the loss of LC norepinephrine (NE), and subsequently its immune modulatory and neuroprotective actions, may exacerbate or even accelerate disease progression. In this review, we discuss the mechanisms by which α-syn pathology and loss of central NE may directly impact brain health by interrupting neurotrophic factor signaling, exacerbating neuroinflammation, and altering regulation of innate and adaptive immune cells. Frontiers Media S.A. 2018-09-11 /pmc/articles/PMC6143806/ /pubmed/30258347 http://dx.doi.org/10.3389/fnins.2018.00626 Text en Copyright © 2018 Butkovich, Houser and Tansey. http://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
Butkovich, Laura M.
Houser, Madelyn C.
Tansey, Malú G.
α-Synuclein and Noradrenergic Modulation of Immune Cells in Parkinson’s Disease Pathogenesis
title α-Synuclein and Noradrenergic Modulation of Immune Cells in Parkinson’s Disease Pathogenesis
title_full α-Synuclein and Noradrenergic Modulation of Immune Cells in Parkinson’s Disease Pathogenesis
title_fullStr α-Synuclein and Noradrenergic Modulation of Immune Cells in Parkinson’s Disease Pathogenesis
title_full_unstemmed α-Synuclein and Noradrenergic Modulation of Immune Cells in Parkinson’s Disease Pathogenesis
title_short α-Synuclein and Noradrenergic Modulation of Immune Cells in Parkinson’s Disease Pathogenesis
title_sort α-synuclein and noradrenergic modulation of immune cells in parkinson’s disease pathogenesis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143806/
https://www.ncbi.nlm.nih.gov/pubmed/30258347
http://dx.doi.org/10.3389/fnins.2018.00626
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