Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytes

Detalhes bibliográficos
Autor(a) principal: Mendes, Alexandrina Ferreira
Data de Publicação: 2003
Outros Autores: Caramona, M. Margarida, Carvalho, A. Pato, Lopes, M. Celeste
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/8363
https://doi.org/10.1002/jcb.10428
Resumo: Our previous studies showed that reactive oxygen species (ROS) are required for the pro-inflammatory cytokine interleukin-1beta (IL-1) to induce the activity of the Nuclear transcription Factor-kappaB (NF-kappaB) and the expression of the inducible isoform of the nitric oxide synthase (iNOS) in bovine articular chondrocytes. This study aimed at elucidating the role of hydrogen peroxide (H2O2) and the superoxide radical, two major ROS, in mediating those IL-1-induced responses. The results obtained show that chondrocytes produce both H2O2 and superoxide radical in response to IL-1. Treatment of the chondrocyte cultures with H2O2 alone did not induce NF-kappaB activation or iNOS expression. Addition of H2O2 simultaneously with IL-1 did neither enhance nor inhibit NF-kappaB activation and iNOS expression, relatively to treatment with IL-1 alone. Accordingly, treatment with catalase did not inhibit those IL-1-induced responses. Treatment with superoxide dismutase, however, effectively prevented IL-1-induced IkappaB-alpha degradation and iNOS expression. Taken together, the results obtained indicate that superoxide mediates IL-1-induced IkappaB-alpha degradation and the consequent NF-kappaB activation and iNOS expression in chondrocytes, whereas H2O2 does not seem to participate in those IL-1-induced responses. In conclusion, the present study identifies the superoxide radical as the ROS involved in mediating the IL-1-induced signaling pathway that leads to NF-kappaB activation and to the expression of NF-kappaB-dependent genes in bovine articular chondrocytes. © 2003 Wiley-Liss, Inc.
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spelling Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytesOur previous studies showed that reactive oxygen species (ROS) are required for the pro-inflammatory cytokine interleukin-1beta (IL-1) to induce the activity of the Nuclear transcription Factor-kappaB (NF-kappaB) and the expression of the inducible isoform of the nitric oxide synthase (iNOS) in bovine articular chondrocytes. This study aimed at elucidating the role of hydrogen peroxide (H2O2) and the superoxide radical, two major ROS, in mediating those IL-1-induced responses. The results obtained show that chondrocytes produce both H2O2 and superoxide radical in response to IL-1. Treatment of the chondrocyte cultures with H2O2 alone did not induce NF-kappaB activation or iNOS expression. Addition of H2O2 simultaneously with IL-1 did neither enhance nor inhibit NF-kappaB activation and iNOS expression, relatively to treatment with IL-1 alone. Accordingly, treatment with catalase did not inhibit those IL-1-induced responses. Treatment with superoxide dismutase, however, effectively prevented IL-1-induced IkappaB-alpha degradation and iNOS expression. Taken together, the results obtained indicate that superoxide mediates IL-1-induced IkappaB-alpha degradation and the consequent NF-kappaB activation and iNOS expression in chondrocytes, whereas H2O2 does not seem to participate in those IL-1-induced responses. In conclusion, the present study identifies the superoxide radical as the ROS involved in mediating the IL-1-induced signaling pathway that leads to NF-kappaB activation and to the expression of NF-kappaB-dependent genes in bovine articular chondrocytes. © 2003 Wiley-Liss, Inc.2003info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/8363http://hdl.handle.net/10316/8363https://doi.org/10.1002/jcb.10428engJournal of Cellular Biochemistry. 88:4 (2003) 783-793Mendes, Alexandrina FerreiraCaramona, M. MargaridaCarvalho, A. PatoLopes, M. Celesteinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-05-27T16:14:30Zoai:estudogeral.uc.pt:10316/8363Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:47:20.444609Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytes
title Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytes
spellingShingle Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytes
Mendes, Alexandrina Ferreira
title_short Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytes
title_full Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytes
title_fullStr Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytes
title_full_unstemmed Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytes
title_sort Differential roles of hydrogen peroxide and superoxide in mediating IL-1-induced NF-kappaB activation and iNOS expression in bovine articular chondrocytes
author Mendes, Alexandrina Ferreira
author_facet Mendes, Alexandrina Ferreira
Caramona, M. Margarida
Carvalho, A. Pato
Lopes, M. Celeste
author_role author
author2 Caramona, M. Margarida
Carvalho, A. Pato
Lopes, M. Celeste
author2_role author
author
author
dc.contributor.author.fl_str_mv Mendes, Alexandrina Ferreira
Caramona, M. Margarida
Carvalho, A. Pato
Lopes, M. Celeste
description Our previous studies showed that reactive oxygen species (ROS) are required for the pro-inflammatory cytokine interleukin-1beta (IL-1) to induce the activity of the Nuclear transcription Factor-kappaB (NF-kappaB) and the expression of the inducible isoform of the nitric oxide synthase (iNOS) in bovine articular chondrocytes. This study aimed at elucidating the role of hydrogen peroxide (H2O2) and the superoxide radical, two major ROS, in mediating those IL-1-induced responses. The results obtained show that chondrocytes produce both H2O2 and superoxide radical in response to IL-1. Treatment of the chondrocyte cultures with H2O2 alone did not induce NF-kappaB activation or iNOS expression. Addition of H2O2 simultaneously with IL-1 did neither enhance nor inhibit NF-kappaB activation and iNOS expression, relatively to treatment with IL-1 alone. Accordingly, treatment with catalase did not inhibit those IL-1-induced responses. Treatment with superoxide dismutase, however, effectively prevented IL-1-induced IkappaB-alpha degradation and iNOS expression. Taken together, the results obtained indicate that superoxide mediates IL-1-induced IkappaB-alpha degradation and the consequent NF-kappaB activation and iNOS expression in chondrocytes, whereas H2O2 does not seem to participate in those IL-1-induced responses. In conclusion, the present study identifies the superoxide radical as the ROS involved in mediating the IL-1-induced signaling pathway that leads to NF-kappaB activation and to the expression of NF-kappaB-dependent genes in bovine articular chondrocytes. © 2003 Wiley-Liss, Inc.
publishDate 2003
dc.date.none.fl_str_mv 2003
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http://hdl.handle.net/10316/8363
https://doi.org/10.1002/jcb.10428
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https://doi.org/10.1002/jcb.10428
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dc.relation.none.fl_str_mv Journal of Cellular Biochemistry. 88:4 (2003) 783-793
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