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Poly(ADP-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging

Poly(ADP-ribose) polymerase 1 (PARP1) is a chromatin-associated nuclear protein, which functions as molecular stress sensor. Reactive oxygen species, responsible for the most plausible and currently acceptable global mechanism to explain the aging process, strongly activate the enzymatic activity of...

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Detalles Bibliográficos
Autores principales: Altmeyer, Matthias, Hottiger, Michael O.
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806023/
https://www.ncbi.nlm.nih.gov/pubmed/20157531
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author Altmeyer, Matthias
Hottiger, Michael O.
author_facet Altmeyer, Matthias
Hottiger, Michael O.
author_sort Altmeyer, Matthias
collection PubMed
description Poly(ADP-ribose) polymerase 1 (PARP1) is a chromatin-associated nuclear protein, which functions as molecular stress sensor. Reactive oxygen species, responsible for the most plausible and currently acceptable global mechanism to explain the aging process, strongly activate the enzymatic activity of PARP1 and the formation of poly(ADP-ribose) (PAR) from NAD(+). Consumption of NAD(+) links PARP1 to energy metabolism and to a large number of NAD(+)-dependent enzymes, such as the sirtuins. As transcriptional cofactor for NF-κB-dependent gene expression, PARP1 is also connected to the immune response, which is implicated in almost all age-related or associated diseases. Accordingly, numerous experimental studies have demonstrated the beneficial effects of PARP inhibition for several age-related diseases. This review summarizes recent findings on PARP1 and puts them in the context of metabolic stress and inflammation in aging.
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spelling pubmed-28060232010-02-12 Poly(ADP-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging Altmeyer, Matthias Hottiger, Michael O. Aging (Albany NY) Review Poly(ADP-ribose) polymerase 1 (PARP1) is a chromatin-associated nuclear protein, which functions as molecular stress sensor. Reactive oxygen species, responsible for the most plausible and currently acceptable global mechanism to explain the aging process, strongly activate the enzymatic activity of PARP1 and the formation of poly(ADP-ribose) (PAR) from NAD(+). Consumption of NAD(+) links PARP1 to energy metabolism and to a large number of NAD(+)-dependent enzymes, such as the sirtuins. As transcriptional cofactor for NF-κB-dependent gene expression, PARP1 is also connected to the immune response, which is implicated in almost all age-related or associated diseases. Accordingly, numerous experimental studies have demonstrated the beneficial effects of PARP inhibition for several age-related diseases. This review summarizes recent findings on PARP1 and puts them in the context of metabolic stress and inflammation in aging. Impact Journals LLC 2009-05-20 /pmc/articles/PMC2806023/ /pubmed/20157531 Text en Copyright: ©2009 Altmeyer et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Altmeyer, Matthias
Hottiger, Michael O.
Poly(ADP-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging
title Poly(ADP-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging
title_full Poly(ADP-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging
title_fullStr Poly(ADP-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging
title_full_unstemmed Poly(ADP-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging
title_short Poly(ADP-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging
title_sort poly(adp-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806023/
https://www.ncbi.nlm.nih.gov/pubmed/20157531
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