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Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration

Inflammation is increasingly implicated in neurodegenerative disease pathology. As no acquired pathogen appears to drive this inflammation, the question of what does remains. Recent advances indicate damage-associated molecular pattern (DAMP) molecules, which are released by injured and dying cells,...

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Autores principales: Wilkins, Heather M., Weidling, Ian W., Ji, Yan, Swerdlow, Russell H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405073/
https://www.ncbi.nlm.nih.gov/pubmed/28491064
http://dx.doi.org/10.3389/fimmu.2017.00508
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author Wilkins, Heather M.
Weidling, Ian W.
Ji, Yan
Swerdlow, Russell H.
author_facet Wilkins, Heather M.
Weidling, Ian W.
Ji, Yan
Swerdlow, Russell H.
author_sort Wilkins, Heather M.
collection PubMed
description Inflammation is increasingly implicated in neurodegenerative disease pathology. As no acquired pathogen appears to drive this inflammation, the question of what does remains. Recent advances indicate damage-associated molecular pattern (DAMP) molecules, which are released by injured and dying cells, can cause specific inflammatory cascades. Inflammation, therefore, can be endogenously induced. Mitochondrial components induce inflammatory responses in several pathological conditions. Due to evidence such as this, a number of mitochondrial components, including mitochondrial DNA, have been labeled as DAMP molecules. In this review, we consider the contributions of mitochondrial-derived DAMPs to inflammation observed in neurodegenerative diseases.
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spelling pubmed-54050732017-05-10 Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration Wilkins, Heather M. Weidling, Ian W. Ji, Yan Swerdlow, Russell H. Front Immunol Immunology Inflammation is increasingly implicated in neurodegenerative disease pathology. As no acquired pathogen appears to drive this inflammation, the question of what does remains. Recent advances indicate damage-associated molecular pattern (DAMP) molecules, which are released by injured and dying cells, can cause specific inflammatory cascades. Inflammation, therefore, can be endogenously induced. Mitochondrial components induce inflammatory responses in several pathological conditions. Due to evidence such as this, a number of mitochondrial components, including mitochondrial DNA, have been labeled as DAMP molecules. In this review, we consider the contributions of mitochondrial-derived DAMPs to inflammation observed in neurodegenerative diseases. Frontiers Media S.A. 2017-04-26 /pmc/articles/PMC5405073/ /pubmed/28491064 http://dx.doi.org/10.3389/fimmu.2017.00508 Text en Copyright © 2017 Wilkins, Weidling, Ji and Swerdlow. 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) or licensor 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 Immunology
Wilkins, Heather M.
Weidling, Ian W.
Ji, Yan
Swerdlow, Russell H.
Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration
title Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration
title_full Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration
title_fullStr Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration
title_full_unstemmed Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration
title_short Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration
title_sort mitochondria-derived damage-associated molecular patterns in neurodegeneration
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405073/
https://www.ncbi.nlm.nih.gov/pubmed/28491064
http://dx.doi.org/10.3389/fimmu.2017.00508
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