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Proteomic analysis of total cellular proteins of human neutrophils

BACKGROUND: Neutrophils are the most abundant leukocytes in peripheral blood and represent one of the most important elements of innate immunity. Recent subcellular proteomic studies have focused on the identification of human neutrophil proteins in various subcellular membrane and granular fraction...

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Autores principales: Tomazella, Gisele G, da Silva, Idalete, Laure, Helen J, Rosa, José C, Chammas, Roger, Wiker, Harald G, de Souza, Gustavo A, Greene, Lewis J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224919/
https://www.ncbi.nlm.nih.gov/pubmed/19719850
http://dx.doi.org/10.1186/1477-5956-7-32
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author Tomazella, Gisele G
da Silva, Idalete
Laure, Helen J
Rosa, José C
Chammas, Roger
Wiker, Harald G
de Souza, Gustavo A
Greene, Lewis J
author_facet Tomazella, Gisele G
da Silva, Idalete
Laure, Helen J
Rosa, José C
Chammas, Roger
Wiker, Harald G
de Souza, Gustavo A
Greene, Lewis J
author_sort Tomazella, Gisele G
collection PubMed
description BACKGROUND: Neutrophils are the most abundant leukocytes in peripheral blood and represent one of the most important elements of innate immunity. Recent subcellular proteomic studies have focused on the identification of human neutrophil proteins in various subcellular membrane and granular fractions. Although there are relatively few studies dealing with the analysis of the total extract of human neutrophils, many biological problems such as the role of chemokines, adhesion molecules, and other activating inputs involved in neutrophil responses and signaling can be approached on the basis of the identification of the total cellular proteins. RESULTS: Using gel-LC-MS/MS, 251 total cellular proteins were identified from resting human neutrophils. This is more than ten times the number of proteins identified by an initial proteome analysis of human neutrophils and almost five times the number of proteins identified by the first 2-DE map of extracts of rat polymorphonuclear leukocytes. Most of the proteins identified in the present study are well-known, but some of them, such as neutrophil-secreted proteins and centaurin beta-1, a cytoplasmic protein involved in the regulation of NF-κB activity, are described here for the first-time. CONCLUSION: The present report provides new information about the protein content of human neutrophils. Importantly, our study resulted in the discovery of a series of proteins not previously reported to be associated with human neutrophils. These data are relevant to the investigation of comparative pathological states and models for novel classes of pharmaceutical drugs that could be useful in the treatment of inflammatory disorders in which neutrophils participate.
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spelling pubmed-32249192011-11-29 Proteomic analysis of total cellular proteins of human neutrophils Tomazella, Gisele G da Silva, Idalete Laure, Helen J Rosa, José C Chammas, Roger Wiker, Harald G de Souza, Gustavo A Greene, Lewis J Proteome Sci Research BACKGROUND: Neutrophils are the most abundant leukocytes in peripheral blood and represent one of the most important elements of innate immunity. Recent subcellular proteomic studies have focused on the identification of human neutrophil proteins in various subcellular membrane and granular fractions. Although there are relatively few studies dealing with the analysis of the total extract of human neutrophils, many biological problems such as the role of chemokines, adhesion molecules, and other activating inputs involved in neutrophil responses and signaling can be approached on the basis of the identification of the total cellular proteins. RESULTS: Using gel-LC-MS/MS, 251 total cellular proteins were identified from resting human neutrophils. This is more than ten times the number of proteins identified by an initial proteome analysis of human neutrophils and almost five times the number of proteins identified by the first 2-DE map of extracts of rat polymorphonuclear leukocytes. Most of the proteins identified in the present study are well-known, but some of them, such as neutrophil-secreted proteins and centaurin beta-1, a cytoplasmic protein involved in the regulation of NF-κB activity, are described here for the first-time. CONCLUSION: The present report provides new information about the protein content of human neutrophils. Importantly, our study resulted in the discovery of a series of proteins not previously reported to be associated with human neutrophils. These data are relevant to the investigation of comparative pathological states and models for novel classes of pharmaceutical drugs that could be useful in the treatment of inflammatory disorders in which neutrophils participate. BioMed Central 2009-08-31 /pmc/articles/PMC3224919/ /pubmed/19719850 http://dx.doi.org/10.1186/1477-5956-7-32 Text en Copyright ©2009 Tomazella 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
Tomazella, Gisele G
da Silva, Idalete
Laure, Helen J
Rosa, José C
Chammas, Roger
Wiker, Harald G
de Souza, Gustavo A
Greene, Lewis J
Proteomic analysis of total cellular proteins of human neutrophils
title Proteomic analysis of total cellular proteins of human neutrophils
title_full Proteomic analysis of total cellular proteins of human neutrophils
title_fullStr Proteomic analysis of total cellular proteins of human neutrophils
title_full_unstemmed Proteomic analysis of total cellular proteins of human neutrophils
title_short Proteomic analysis of total cellular proteins of human neutrophils
title_sort proteomic analysis of total cellular proteins of human neutrophils
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224919/
https://www.ncbi.nlm.nih.gov/pubmed/19719850
http://dx.doi.org/10.1186/1477-5956-7-32
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