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dc.contributor.author
Romani, Arianna
dc.contributor.author
Cervellati, Carlo
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Muresan, Ximena M.
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Belmonte, Giuseppe
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Pecorelli, Alessandra
dc.contributor.author
Cervellati, Franco
dc.contributor.author
Benedusi, Mascia
dc.contributor.author
Evelson, Pablo Andrés

dc.contributor.author
Valacchi, Giuseppe
dc.date.available
2018-06-05T21:09:28Z
dc.date.issued
2017-11
dc.identifier.citation
Romani, Arianna; Cervellati, Carlo; Muresan, Ximena M.; Belmonte, Giuseppe; Pecorelli, Alessandra; et al.; Keratinocytes oxidative damage mechanisms related to airbone particle matter exposure; Elsevier Ireland; Mechanisms of Ageing and Development; 172; 11-2017; 86-95
dc.identifier.issn
0047-6374
dc.identifier.uri
http://hdl.handle.net/11336/47421
dc.description.abstract
Epidemiological evidences have correlated airbone particulate matter (PM) to adverse health effects, mainly linking to pulmonary and cardiovascular disease. Nevertheless, only recently, some studies reported detrimental effects of PM on other organs such as skin. In a recent work, we have reported increased oxidative and inflammatory responses in Reconstituted Human Epidermis (RHE) exposed to ambient particles (CAPs) and we also demonstrated the ability of CAPs to penetrate the skin tissue.The present study was aimed to better understand the cellular mechanisms beyond the oxidative changes induced by CAPs (5-10-25. μg/mL) in human immortalized keratinocytes (HaCaT).After 24. h of treatment, CAPs were able to enter the cells leading to a decrease in viability, increased levels of 4-hydroxinonenal products (4-HNE) and IL-1α release. Overall these data, suggest lipid and protein oxidative damage, as well as an increase of inflammatory response after being challenged with CAPs. In addition, 3. h after CAPs exposure we found a significant increase in NF-kB and Nrf2 translocation into the nucleus. In contrast, no differences in gene expression and enzymatic activity of Nrf2 target genes were detected. This last finding could be explained by the ability of CAPs to possibly alter the binding of Nrf2 to the ARE DNA sequence.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Elsevier Ireland

dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
AIR POLLUTION
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INFLAMMATION
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OXIDATIVE DAMAGE
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PARTICULATE MATTER
dc.subject.classification
Salud Ocupacional

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Ciencias de la Salud

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CIENCIAS MÉDICAS Y DE LA SALUD

dc.title
Keratinocytes oxidative damage mechanisms related to airbone particle matter exposure
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2018-06-05T20:07:05Z
dc.journal.volume
172
dc.journal.pagination
86-95
dc.journal.pais
Irlanda

dc.journal.ciudad
Shannon
dc.description.fil
Fil: Romani, Arianna. Università di Ferrara; Italia
dc.description.fil
Fil: Cervellati, Carlo. Università di Ferrara; Italia
dc.description.fil
Fil: Muresan, Ximena M.. Università di Ferrara; Italia
dc.description.fil
Fil: Belmonte, Giuseppe. Università di Ferrara; Italia
dc.description.fil
Fil: Pecorelli, Alessandra. North Carolina State University; Estados Unidos
dc.description.fil
Fil: Cervellati, Franco. Università di Ferrara; Italia
dc.description.fil
Fil: Benedusi, Mascia. Università di Ferrara; Italia
dc.description.fil
Fil: Evelson, Pablo Andrés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular. Departamento de Patología; Argentina
dc.description.fil
Fil: Valacchi, Giuseppe. Università di Ferrara; Italia. North Carolina State University; Estados Unidos
dc.journal.title
Mechanisms of Ageing and Development

dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.mad.2017.11.007
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0047637417300830
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