Increased ROS production and DNA damage in monocytes are biomarkers of aging and atherosclerosis

Abstract Background: New evidence demonstrates that aging and dyslipidemia are closely associated with oxidative stress, DNA damage and apoptosis in some cells and extravascular tissues. However, in monocytes, which are naturally involved in progression and/or resolution of plaque in atherosclerosi...

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Autores principales: Jacinto,Thais A., Meireles,Giselle S., Dias,Ananda T., Aires,Rafaela, Porto,Marcella L., Gava,Agata L., Vasquez,Elisardo C., Pereira,Thiago Melo C., Campagnaro,Bianca P., Meyrelles,Silvana S.
Lenguaje:English
Publicado: Sociedad de Biología de Chile 2018
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602018000100228
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spelling oai:scielo:S0716-976020180001002282018-10-18Increased ROS production and DNA damage in monocytes are biomarkers of aging and atherosclerosisJacinto,Thais A.Meireles,Giselle S.Dias,Ananda T.Aires,RafaelaPorto,Marcella L.Gava,Agata L.Vasquez,Elisardo C.Pereira,Thiago Melo C.Campagnaro,Bianca P.Meyrelles,Silvana S. apoE knockout mice Atherosclerosis Proinflammatory cytokines Apoptosis Abstract Background: New evidence demonstrates that aging and dyslipidemia are closely associated with oxidative stress, DNA damage and apoptosis in some cells and extravascular tissues. However, in monocytes, which are naturally involved in progression and/or resolution of plaque in atherosclerosis, this concurrence has not yet been fully investigated. In this study, we evaluated the influence of aging and hypercholesterolemia on serum pro-inflammatory cytokines, oxidative stress, DNA damage and apoptosis in monocytes from apolipoprotein E-deficient (apoE-/-) mice compared with age-matched wild-type C57BL/6 (WT) mice. Experiments were performed in young (2-months) and in old (18-months) male wild-type (WT) and apoE-/- mice. Results: Besides the expected differences in serum lipid profile and plaque formation, we observed that atherosclerotic mice exhibited a significant increase in monocytosis and in serum levels of pro-inflammatory cytokines compared to WT mice. Moreover, it was observed that the overproduction of ROS, led to an increased DNA fragmentation and, consequently, apoptosis in monocytes from normocholesterolemic old mice, which was aggravated in age-matched atherosclerotic mice. Conclusions: In this study, we demonstrate that a pro-inflammatory systemic status is associated with an impairment of functionality of monocytes during aging and that these parameters are fundamental extra-arterial contributors to the aggravation of atherosclerosis. The present data open new avenues for the development of future strategies with the purpose of treating atherosclerosis.info:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.51 20182018-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602018000100228en10.1186/s40659-018-0182-7
institution Scielo Chile
collection Scielo Chile
language English
topic apoE knockout mice
Atherosclerosis
Proinflammatory cytokines
Apoptosis
spellingShingle apoE knockout mice
Atherosclerosis
Proinflammatory cytokines
Apoptosis
Jacinto,Thais A.
Meireles,Giselle S.
Dias,Ananda T.
Aires,Rafaela
Porto,Marcella L.
Gava,Agata L.
Vasquez,Elisardo C.
Pereira,Thiago Melo C.
Campagnaro,Bianca P.
Meyrelles,Silvana S.
Increased ROS production and DNA damage in monocytes are biomarkers of aging and atherosclerosis
description Abstract Background: New evidence demonstrates that aging and dyslipidemia are closely associated with oxidative stress, DNA damage and apoptosis in some cells and extravascular tissues. However, in monocytes, which are naturally involved in progression and/or resolution of plaque in atherosclerosis, this concurrence has not yet been fully investigated. In this study, we evaluated the influence of aging and hypercholesterolemia on serum pro-inflammatory cytokines, oxidative stress, DNA damage and apoptosis in monocytes from apolipoprotein E-deficient (apoE-/-) mice compared with age-matched wild-type C57BL/6 (WT) mice. Experiments were performed in young (2-months) and in old (18-months) male wild-type (WT) and apoE-/- mice. Results: Besides the expected differences in serum lipid profile and plaque formation, we observed that atherosclerotic mice exhibited a significant increase in monocytosis and in serum levels of pro-inflammatory cytokines compared to WT mice. Moreover, it was observed that the overproduction of ROS, led to an increased DNA fragmentation and, consequently, apoptosis in monocytes from normocholesterolemic old mice, which was aggravated in age-matched atherosclerotic mice. Conclusions: In this study, we demonstrate that a pro-inflammatory systemic status is associated with an impairment of functionality of monocytes during aging and that these parameters are fundamental extra-arterial contributors to the aggravation of atherosclerosis. The present data open new avenues for the development of future strategies with the purpose of treating atherosclerosis.
author Jacinto,Thais A.
Meireles,Giselle S.
Dias,Ananda T.
Aires,Rafaela
Porto,Marcella L.
Gava,Agata L.
Vasquez,Elisardo C.
Pereira,Thiago Melo C.
Campagnaro,Bianca P.
Meyrelles,Silvana S.
author_facet Jacinto,Thais A.
Meireles,Giselle S.
Dias,Ananda T.
Aires,Rafaela
Porto,Marcella L.
Gava,Agata L.
Vasquez,Elisardo C.
Pereira,Thiago Melo C.
Campagnaro,Bianca P.
Meyrelles,Silvana S.
author_sort Jacinto,Thais A.
title Increased ROS production and DNA damage in monocytes are biomarkers of aging and atherosclerosis
title_short Increased ROS production and DNA damage in monocytes are biomarkers of aging and atherosclerosis
title_full Increased ROS production and DNA damage in monocytes are biomarkers of aging and atherosclerosis
title_fullStr Increased ROS production and DNA damage in monocytes are biomarkers of aging and atherosclerosis
title_full_unstemmed Increased ROS production and DNA damage in monocytes are biomarkers of aging and atherosclerosis
title_sort increased ros production and dna damage in monocytes are biomarkers of aging and atherosclerosis
publisher Sociedad de Biología de Chile
publishDate 2018
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602018000100228
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