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DNA Damage Response and Immune Defense: Links and Mechanisms

DNA damage plays a causal role in numerous human pathologies including cancer, premature aging, and chronic inflammatory conditions. In response to genotoxic insults, the DNA damage response (DDR) orchestrates DNA damage checkpoint activation and facilitates the removal of DNA lesions. The DDR can a...

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Detalles Bibliográficos
Autores principales: Nakad, Rania, Schumacher, Björn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977279/
https://www.ncbi.nlm.nih.gov/pubmed/27555866
http://dx.doi.org/10.3389/fgene.2016.00147
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author Nakad, Rania
Schumacher, Björn
author_facet Nakad, Rania
Schumacher, Björn
author_sort Nakad, Rania
collection PubMed
description DNA damage plays a causal role in numerous human pathologies including cancer, premature aging, and chronic inflammatory conditions. In response to genotoxic insults, the DNA damage response (DDR) orchestrates DNA damage checkpoint activation and facilitates the removal of DNA lesions. The DDR can also arouse the immune system by for example inducing the expression of antimicrobial peptides as well as ligands for receptors found on immune cells. The activation of immune signaling is triggered by different components of the DDR including DNA damage sensors, transducer kinases, and effectors. In this review, we describe recent advances on the understanding of the role of DDR in activating immune signaling. We highlight evidence gained into (i) which molecular and cellular pathways of DDR activate immune signaling, (ii) how DNA damage drives chronic inflammation, and (iii) how chronic inflammation causes DNA damage and pathology in humans.
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spelling pubmed-49772792016-08-23 DNA Damage Response and Immune Defense: Links and Mechanisms Nakad, Rania Schumacher, Björn Front Genet Genetics DNA damage plays a causal role in numerous human pathologies including cancer, premature aging, and chronic inflammatory conditions. In response to genotoxic insults, the DNA damage response (DDR) orchestrates DNA damage checkpoint activation and facilitates the removal of DNA lesions. The DDR can also arouse the immune system by for example inducing the expression of antimicrobial peptides as well as ligands for receptors found on immune cells. The activation of immune signaling is triggered by different components of the DDR including DNA damage sensors, transducer kinases, and effectors. In this review, we describe recent advances on the understanding of the role of DDR in activating immune signaling. We highlight evidence gained into (i) which molecular and cellular pathways of DDR activate immune signaling, (ii) how DNA damage drives chronic inflammation, and (iii) how chronic inflammation causes DNA damage and pathology in humans. Frontiers Media S.A. 2016-08-09 /pmc/articles/PMC4977279/ /pubmed/27555866 http://dx.doi.org/10.3389/fgene.2016.00147 Text en Copyright © 2016 Nakad and Schumacher. 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 Genetics
Nakad, Rania
Schumacher, Björn
DNA Damage Response and Immune Defense: Links and Mechanisms
title DNA Damage Response and Immune Defense: Links and Mechanisms
title_full DNA Damage Response and Immune Defense: Links and Mechanisms
title_fullStr DNA Damage Response and Immune Defense: Links and Mechanisms
title_full_unstemmed DNA Damage Response and Immune Defense: Links and Mechanisms
title_short DNA Damage Response and Immune Defense: Links and Mechanisms
title_sort dna damage response and immune defense: links and mechanisms
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977279/
https://www.ncbi.nlm.nih.gov/pubmed/27555866
http://dx.doi.org/10.3389/fgene.2016.00147
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