Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bernardini, Chiara, Greco, Francesca, Zannoni, Augusta, Bacci, Maria Laura, Seren, Eraldo, Forni, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
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
_version_ 1782255435871420416
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
work_keys_str_mv AT bernardinichiara differentialexpressionofnitricoxidesynthasesinporcineaorticendothelialcellsduringlpsinducedapoptosis
AT grecofrancesca differentialexpressionofnitricoxidesynthasesinporcineaorticendothelialcellsduringlpsinducedapoptosis
AT zannoniaugusta differentialexpressionofnitricoxidesynthasesinporcineaorticendothelialcellsduringlpsinducedapoptosis
AT baccimarialaura differentialexpressionofnitricoxidesynthasesinporcineaorticendothelialcellsduringlpsinducedapoptosis
AT sereneraldo differentialexpressionofnitricoxidesynthasesinporcineaorticendothelialcellsduringlpsinducedapoptosis
AT fornimonica differentialexpressionofnitricoxidesynthasesinporcineaorticendothelialcellsduringlpsinducedapoptosis