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Nucleotide receptor signalling and the generation of reactive oxygen species

Elevated levels of extracellular nucleotides are present at sites of inflammation, platelet degranulation and cellular damage or lysis. These extracellular nucleotides can lead to the activation of purinergic (nucleotide) receptors on various leukocytes, including monocytes, macrophages, eosinophils...

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Detalles Bibliográficos
Autores principales: Guerra, Alma N., Gavala, Monica L., Chung, Hun Sun, Bertics, Paul J.
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2096761/
https://www.ncbi.nlm.nih.gov/pubmed/18404417
http://dx.doi.org/10.1007/s11302-006-9035-x
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author Guerra, Alma N.
Gavala, Monica L.
Chung, Hun Sun
Bertics, Paul J.
author_facet Guerra, Alma N.
Gavala, Monica L.
Chung, Hun Sun
Bertics, Paul J.
author_sort Guerra, Alma N.
collection PubMed
description Elevated levels of extracellular nucleotides are present at sites of inflammation, platelet degranulation and cellular damage or lysis. These extracellular nucleotides can lead to the activation of purinergic (nucleotide) receptors on various leukocytes, including monocytes, macrophages, eosinophils, and neutrophils. In turn, nucleotide receptor activation has been linked to increased cellular production and release of multiple inflammatory mediators, including superoxide anion, nitric oxide and other reactive oxygen species (ROS). In the present review, we will summarize the evidence that extracellular nucleotides can facilitate the generation of multiple ROS by leukocytes. In addition, we will discuss several potential mechanisms by which nucleotide-enhanced ROS production may occur. Delineation of these mechanisms is important for understanding the processes associated with nucleotide-induced antimicrobial activities, cell signalling, apoptosis, and pathology.
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spelling pubmed-20967612008-02-27 Nucleotide receptor signalling and the generation of reactive oxygen species Guerra, Alma N. Gavala, Monica L. Chung, Hun Sun Bertics, Paul J. Purinergic Signal Original Paper Elevated levels of extracellular nucleotides are present at sites of inflammation, platelet degranulation and cellular damage or lysis. These extracellular nucleotides can lead to the activation of purinergic (nucleotide) receptors on various leukocytes, including monocytes, macrophages, eosinophils, and neutrophils. In turn, nucleotide receptor activation has been linked to increased cellular production and release of multiple inflammatory mediators, including superoxide anion, nitric oxide and other reactive oxygen species (ROS). In the present review, we will summarize the evidence that extracellular nucleotides can facilitate the generation of multiple ROS by leukocytes. In addition, we will discuss several potential mechanisms by which nucleotide-enhanced ROS production may occur. Delineation of these mechanisms is important for understanding the processes associated with nucleotide-induced antimicrobial activities, cell signalling, apoptosis, and pathology. Springer Netherlands 2007-01-06 2007-03 /pmc/articles/PMC2096761/ /pubmed/18404417 http://dx.doi.org/10.1007/s11302-006-9035-x Text en © Springer Science + Business Media B.V. 2007
spellingShingle Original Paper
Guerra, Alma N.
Gavala, Monica L.
Chung, Hun Sun
Bertics, Paul J.
Nucleotide receptor signalling and the generation of reactive oxygen species
title Nucleotide receptor signalling and the generation of reactive oxygen species
title_full Nucleotide receptor signalling and the generation of reactive oxygen species
title_fullStr Nucleotide receptor signalling and the generation of reactive oxygen species
title_full_unstemmed Nucleotide receptor signalling and the generation of reactive oxygen species
title_short Nucleotide receptor signalling and the generation of reactive oxygen species
title_sort nucleotide receptor signalling and the generation of reactive oxygen species
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2096761/
https://www.ncbi.nlm.nih.gov/pubmed/18404417
http://dx.doi.org/10.1007/s11302-006-9035-x
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