Age-dependent regulation of antioxidant genes by p38α MAPK in the liver

p38α is a redox sensitive MAPK activated by pro-inflammatory cytokines and environmental, genotoxic and endoplasmic reticulum stresses. The aim of this work was to assess whether p38α controls the antioxidant defense in the liver, and if so, to elucidate the mechanism(s) involved and the age-related...

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Main Authors: Salvador Pérez, Sergio Rius-Pérez, Ana M. Tormos, Isabela Finamor, Ángel R. Nebreda, Raquel Taléns-Visconti, Juan Sastre
Format: Article
Language:English
Published: Elsevier 2018-06-01
Series:Redox Biology
Online Access:http://www.sciencedirect.com/science/article/pii/S2213231717309655
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spelling doaj-af101cae690c4f3fbbb762e9e4f8d37b2020-11-24T21:56:33ZengElsevierRedox Biology2213-23172018-06-0116276284Age-dependent regulation of antioxidant genes by p38α MAPK in the liverSalvador Pérez0Sergio Rius-Pérez1Ana M. Tormos2Isabela Finamor3Ángel R. Nebreda4Raquel Taléns-Visconti5Juan Sastre6Department of Physiology, School of Pharmacy, University of Valencia, Burjassot, 46100 SpainDepartment of Physiology, School of Pharmacy, University of Valencia, Burjassot, 46100 SpainDepartment of Physiology, School of Pharmacy, University of Valencia, Burjassot, 46100 SpainDepartment of Physiology, School of Pharmacy, University of Valencia, Burjassot, 46100 SpainInstitute for Research in Biomedicine (IRB Barcelona), Barcelona Institute of Science and Technology, 08028 Barcelona, Spain; ICREA, Pg. Lluís Companys 23, 08010, Barcelona, SpainDepartment of Pharmacy and Pharmaceutical Technology and Parasitology, School of Pharmacy, University of Valencia, Burjassot, 46100 SpainDepartment of Physiology, School of Pharmacy, University of Valencia, Burjassot, 46100 Spain; Correspondence to: Department of Physiology, School of Pharmacy, University of Valencia, Avda. Vicente Andres Estelles s/n, 46100 Burjasot (Valencia), Spain.p38α is a redox sensitive MAPK activated by pro-inflammatory cytokines and environmental, genotoxic and endoplasmic reticulum stresses. The aim of this work was to assess whether p38α controls the antioxidant defense in the liver, and if so, to elucidate the mechanism(s) involved and the age-related changes. For this purpose, we used liver-specific p38α-deficient mice at two different ages: young-mice (4 months-old) and old-mice (24 months-old). The liver of young p38α knock-out mice exhibited a decrease in GSH levels and an increase in GSSG/GSH ratio and malondialdehyde levels. However, old mice deficient in p38α had higher hepatic GSH levels and lower GSSG/GSH ratio than young p38α knock-out mice. Liver-specific p38α deficiency triggered a dramatic down-regulation of the mRNAs of the key antioxidant enzymes glutamate cysteine ligase, superoxide dismutase 1, superoxide dismutase 2, and catalase in young mice, which seems mediated by the lack of p65 recruitment to their promoters. Nrf-2 nuclear levels did not change significantly in the liver of young mice upon p38α deficiency, but nuclear levels of phospho-p65 and PGC-1α decreased in these mice. p38α-dependent activation of NF-κB seems to occur through classical IκB Kinase and via ribosomal S6 kinase1 and AKT in young mice. However, unexpectedly the long-term deficiency in p38α triggers a compensatory up-regulation of antioxidant enzymes via NF-κB activation and recruitment of p65 to their promoters. In conclusion, p38α MAPK maintains the expression of antioxidant genes in liver of young animals via NF-κΒ under basal conditions, whereas its long-term deficiency triggers compensatory up-regulation of antioxidant enzymes through NF-κΒ. Keywords: Nuclear factor ƙB, Glutathione, Glutamate cysteine ligase, Superoxide dismutase 1, Superoxide dismutase 2, And catalasehttp://www.sciencedirect.com/science/article/pii/S2213231717309655
collection DOAJ
language English
format Article
sources DOAJ
author Salvador Pérez
Sergio Rius-Pérez
Ana M. Tormos
Isabela Finamor
Ángel R. Nebreda
Raquel Taléns-Visconti
Juan Sastre
spellingShingle Salvador Pérez
Sergio Rius-Pérez
Ana M. Tormos
Isabela Finamor
Ángel R. Nebreda
Raquel Taléns-Visconti
Juan Sastre
Age-dependent regulation of antioxidant genes by p38α MAPK in the liver
Redox Biology
author_facet Salvador Pérez
Sergio Rius-Pérez
Ana M. Tormos
Isabela Finamor
Ángel R. Nebreda
Raquel Taléns-Visconti
Juan Sastre
author_sort Salvador Pérez
title Age-dependent regulation of antioxidant genes by p38α MAPK in the liver
title_short Age-dependent regulation of antioxidant genes by p38α MAPK in the liver
title_full Age-dependent regulation of antioxidant genes by p38α MAPK in the liver
title_fullStr Age-dependent regulation of antioxidant genes by p38α MAPK in the liver
title_full_unstemmed Age-dependent regulation of antioxidant genes by p38α MAPK in the liver
title_sort age-dependent regulation of antioxidant genes by p38α mapk in the liver
publisher Elsevier
series Redox Biology
issn 2213-2317
publishDate 2018-06-01
description p38α is a redox sensitive MAPK activated by pro-inflammatory cytokines and environmental, genotoxic and endoplasmic reticulum stresses. The aim of this work was to assess whether p38α controls the antioxidant defense in the liver, and if so, to elucidate the mechanism(s) involved and the age-related changes. For this purpose, we used liver-specific p38α-deficient mice at two different ages: young-mice (4 months-old) and old-mice (24 months-old). The liver of young p38α knock-out mice exhibited a decrease in GSH levels and an increase in GSSG/GSH ratio and malondialdehyde levels. However, old mice deficient in p38α had higher hepatic GSH levels and lower GSSG/GSH ratio than young p38α knock-out mice. Liver-specific p38α deficiency triggered a dramatic down-regulation of the mRNAs of the key antioxidant enzymes glutamate cysteine ligase, superoxide dismutase 1, superoxide dismutase 2, and catalase in young mice, which seems mediated by the lack of p65 recruitment to their promoters. Nrf-2 nuclear levels did not change significantly in the liver of young mice upon p38α deficiency, but nuclear levels of phospho-p65 and PGC-1α decreased in these mice. p38α-dependent activation of NF-κB seems to occur through classical IκB Kinase and via ribosomal S6 kinase1 and AKT in young mice. However, unexpectedly the long-term deficiency in p38α triggers a compensatory up-regulation of antioxidant enzymes via NF-κB activation and recruitment of p65 to their promoters. In conclusion, p38α MAPK maintains the expression of antioxidant genes in liver of young animals via NF-κΒ under basal conditions, whereas its long-term deficiency triggers compensatory up-regulation of antioxidant enzymes through NF-κΒ. Keywords: Nuclear factor ƙB, Glutathione, Glutamate cysteine ligase, Superoxide dismutase 1, Superoxide dismutase 2, And catalase
url http://www.sciencedirect.com/science/article/pii/S2213231717309655
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