Flow Cytometric Evaluation of Human Neutrophil Apoptosis During Nitric Oxide Generation In Vitro: The Role of Exogenous Antioxidants

Among numerous inflammatory mediators a nitric oxide molecule is supposed to be important in the modulation of neutrophil survival in vivo and in vitro. The effect of exogenous supply of NO donors such as SNP, SIN-1, and GEA-3162 on the course of human neutrophil apoptosis and the role of extracellu...

Full description

Saved in:
Bibliographic Details
Main Authors: Zofia Sulowska, Ewa Majewska, Magdalena Klink, Malgorzata Banasik, Henryk Tchórzewski
Format: Article
Language:English
Published: Wiley 2005-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/MI.2005.81
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850233781583085568
author Zofia Sulowska
Ewa Majewska
Magdalena Klink
Malgorzata Banasik
Henryk Tchórzewski
author_facet Zofia Sulowska
Ewa Majewska
Magdalena Klink
Malgorzata Banasik
Henryk Tchórzewski
author_sort Zofia Sulowska
collection DOAJ
description Among numerous inflammatory mediators a nitric oxide molecule is supposed to be important in the modulation of neutrophil survival in vivo and in vitro. The effect of exogenous supply of NO donors such as SNP, SIN-1, and GEA-3162 on the course of human neutrophil apoptosis and the role of extracellular antioxidants in this process was investigated. Isolated from peripheral blood, neutrophils were cultured in the presence or absence of NO donor compounds and antioxidants for 8, 12, and 20 hours. Apoptosis of neutrophils was determined in vitro by flow cytometric analysis of cellular DNA content and Annexin V protein binding to the cell surface. Exposure of human neutrophils to GEA-3162 and SIN-1 significantly accelerates and enhances their apoptosis in vitro in a time-dependent fashion. In the presence of SNP, intensification of apoptosis has not been revealed until 12 hours after the culture. The inhibition of GEA-3162- and SIN-1-mediated neutrophil apoptosis by superoxide dismutase (SOD) but not by catalase (CAT) was observed. Our results show that SOD and CAT can protect neutrophils against NO-donors-induced apoptosis and suggest that the interaction of NO and oxygen metabolites signals may determine the destructive or protective role of NO donor compounds during apoptotic neutrophil death.
format Article
id doaj-art-06dbe4ec57574e15815469b51bfb894b
institution OA Journals
issn 0962-9351
1466-1861
language English
publishDate 2005-01-01
publisher Wiley
record_format Article
series Mediators of Inflammation
spelling doaj-art-06dbe4ec57574e15815469b51bfb894b2025-08-20T02:02:51ZengWileyMediators of Inflammation0962-93511466-18612005-01-0120052818710.1155/MI.2005.81Flow Cytometric Evaluation of Human Neutrophil Apoptosis During Nitric Oxide Generation In Vitro: The Role of Exogenous AntioxidantsZofia Sulowska0Ewa Majewska1Magdalena Klink2Malgorzata Banasik3Henryk Tchórzewski4Center for Medical Biology, Polish Academy of Sciences, Lodz 93-232, PolandDepartment of Laboratory Diagnostic and Clinical Biochemistry, Medical University, Lodz 90-153, PolandCenter for Medical Biology, Polish Academy of Sciences, Lodz 93-232, PolandDepartment of Clinical Immunology, Polish Mother's Memorial Institute, Lodz 93-338, PolandDepartment of Clinical Immunology, Polish Mother's Memorial Institute, Lodz 93-338, PolandAmong numerous inflammatory mediators a nitric oxide molecule is supposed to be important in the modulation of neutrophil survival in vivo and in vitro. The effect of exogenous supply of NO donors such as SNP, SIN-1, and GEA-3162 on the course of human neutrophil apoptosis and the role of extracellular antioxidants in this process was investigated. Isolated from peripheral blood, neutrophils were cultured in the presence or absence of NO donor compounds and antioxidants for 8, 12, and 20 hours. Apoptosis of neutrophils was determined in vitro by flow cytometric analysis of cellular DNA content and Annexin V protein binding to the cell surface. Exposure of human neutrophils to GEA-3162 and SIN-1 significantly accelerates and enhances their apoptosis in vitro in a time-dependent fashion. In the presence of SNP, intensification of apoptosis has not been revealed until 12 hours after the culture. The inhibition of GEA-3162- and SIN-1-mediated neutrophil apoptosis by superoxide dismutase (SOD) but not by catalase (CAT) was observed. Our results show that SOD and CAT can protect neutrophils against NO-donors-induced apoptosis and suggest that the interaction of NO and oxygen metabolites signals may determine the destructive or protective role of NO donor compounds during apoptotic neutrophil death.http://dx.doi.org/10.1155/MI.2005.81
spellingShingle Zofia Sulowska
Ewa Majewska
Magdalena Klink
Malgorzata Banasik
Henryk Tchórzewski
Flow Cytometric Evaluation of Human Neutrophil Apoptosis During Nitric Oxide Generation In Vitro: The Role of Exogenous Antioxidants
Mediators of Inflammation
title Flow Cytometric Evaluation of Human Neutrophil Apoptosis During Nitric Oxide Generation In Vitro: The Role of Exogenous Antioxidants
title_full Flow Cytometric Evaluation of Human Neutrophil Apoptosis During Nitric Oxide Generation In Vitro: The Role of Exogenous Antioxidants
title_fullStr Flow Cytometric Evaluation of Human Neutrophil Apoptosis During Nitric Oxide Generation In Vitro: The Role of Exogenous Antioxidants
title_full_unstemmed Flow Cytometric Evaluation of Human Neutrophil Apoptosis During Nitric Oxide Generation In Vitro: The Role of Exogenous Antioxidants
title_short Flow Cytometric Evaluation of Human Neutrophil Apoptosis During Nitric Oxide Generation In Vitro: The Role of Exogenous Antioxidants
title_sort flow cytometric evaluation of human neutrophil apoptosis during nitric oxide generation in vitro the role of exogenous antioxidants
url http://dx.doi.org/10.1155/MI.2005.81
work_keys_str_mv AT zofiasulowska flowcytometricevaluationofhumanneutrophilapoptosisduringnitricoxidegenerationinvitrotheroleofexogenousantioxidants
AT ewamajewska flowcytometricevaluationofhumanneutrophilapoptosisduringnitricoxidegenerationinvitrotheroleofexogenousantioxidants
AT magdalenaklink flowcytometricevaluationofhumanneutrophilapoptosisduringnitricoxidegenerationinvitrotheroleofexogenousantioxidants
AT malgorzatabanasik flowcytometricevaluationofhumanneutrophilapoptosisduringnitricoxidegenerationinvitrotheroleofexogenousantioxidants
AT henryktchorzewski flowcytometricevaluationofhumanneutrophilapoptosisduringnitricoxidegenerationinvitrotheroleofexogenousantioxidants