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Differential expression of nitric oxide synthases in porcine aortic endothelial cells during LPS-induced apoptosis
BACKGROUND: It is well known that nitric oxide (NO) is generated by a family of constitutively (nNOS and eNOS) or inducibly (iNOS) expressed enzymes and takes part in different aspects of the inflammatory response; nevertheless, its effective role in the pathogenesis of multiple organ dysfunction an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542028/ https://www.ncbi.nlm.nih.gov/pubmed/23181483 http://dx.doi.org/10.1186/1476-9255-9-47 |
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author | Bernardini, Chiara Greco, Francesca Zannoni, Augusta Bacci, Maria Laura Seren, Eraldo Forni, Monica |
author_facet | Bernardini, Chiara Greco, Francesca Zannoni, Augusta Bacci, Maria Laura Seren, Eraldo Forni, Monica |
author_sort | Bernardini, Chiara |
collection | PubMed |
description | BACKGROUND: It is well known that nitric oxide (NO) is generated by a family of constitutively (nNOS and eNOS) or inducibly (iNOS) expressed enzymes and takes part in different aspects of the inflammatory response; nevertheless, its effective role in the pathogenesis of multiple organ dysfunction and septic shock is not fully understood. METHODS: To investigate the Nitric Oxide Synthases (NOSs) expression in endothelial cells during endotoxin exposure and the involvement of NO in lipopolysaccharide (LPS)-induced apoptosis, primary cultures of porcine Aortic Endothelial Cells (pAECs) were exposed to LPS for different time periods (1-24 h) and to LPS + L-NAME (15 h). RESULTS: Lipopolysaccharide induced an increase in mRNA and protein iNOS expression; on the contrary, the expression of eNOS was decreased. Furthermore, NOSs localisation was in part modified by LPS treatment. No alteration in the total level of Nitric Oxide was observed. L-NAME (5 mM) addition determined a slight decrease of LPS-induced apoptosis. CONCLUSIONS: Endotoxin treatment strongly influenced NOS expression with an upregulation of iNOS and a simultaneous down regulation of eNOS. Moreover, in our model, the involvement of NO on LPS-induced apoptosis is very modest, suggesting that different pathways are involved in the regulation of this process. |
format | Online Article Text |
id | pubmed-3542028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35420282013-01-11 Differential expression of nitric oxide synthases in porcine aortic endothelial cells during LPS-induced apoptosis Bernardini, Chiara Greco, Francesca Zannoni, Augusta Bacci, Maria Laura Seren, Eraldo Forni, Monica J Inflamm (Lond) Research BACKGROUND: It is well known that nitric oxide (NO) is generated by a family of constitutively (nNOS and eNOS) or inducibly (iNOS) expressed enzymes and takes part in different aspects of the inflammatory response; nevertheless, its effective role in the pathogenesis of multiple organ dysfunction and septic shock is not fully understood. METHODS: To investigate the Nitric Oxide Synthases (NOSs) expression in endothelial cells during endotoxin exposure and the involvement of NO in lipopolysaccharide (LPS)-induced apoptosis, primary cultures of porcine Aortic Endothelial Cells (pAECs) were exposed to LPS for different time periods (1-24 h) and to LPS + L-NAME (15 h). RESULTS: Lipopolysaccharide induced an increase in mRNA and protein iNOS expression; on the contrary, the expression of eNOS was decreased. Furthermore, NOSs localisation was in part modified by LPS treatment. No alteration in the total level of Nitric Oxide was observed. L-NAME (5 mM) addition determined a slight decrease of LPS-induced apoptosis. CONCLUSIONS: Endotoxin treatment strongly influenced NOS expression with an upregulation of iNOS and a simultaneous down regulation of eNOS. Moreover, in our model, the involvement of NO on LPS-induced apoptosis is very modest, suggesting that different pathways are involved in the regulation of this process. BioMed Central 2012-11-26 /pmc/articles/PMC3542028/ /pubmed/23181483 http://dx.doi.org/10.1186/1476-9255-9-47 Text en Copyright ©2012 Bernardini et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Bernardini, Chiara Greco, Francesca Zannoni, Augusta Bacci, Maria Laura Seren, Eraldo Forni, Monica Differential expression of nitric oxide synthases in porcine aortic endothelial cells during LPS-induced apoptosis |
title | Differential expression of nitric oxide synthases in porcine aortic endothelial cells during LPS-induced apoptosis |
title_full | Differential expression of nitric oxide synthases in porcine aortic endothelial cells during LPS-induced apoptosis |
title_fullStr | Differential expression of nitric oxide synthases in porcine aortic endothelial cells during LPS-induced apoptosis |
title_full_unstemmed | Differential expression of nitric oxide synthases in porcine aortic endothelial cells during LPS-induced apoptosis |
title_short | Differential expression of nitric oxide synthases in porcine aortic endothelial cells during LPS-induced apoptosis |
title_sort | differential expression of nitric oxide synthases in porcine aortic endothelial cells during lps-induced apoptosis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542028/ https://www.ncbi.nlm.nih.gov/pubmed/23181483 http://dx.doi.org/10.1186/1476-9255-9-47 |
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