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Leukotriene B(4)-loaded microspheres: a new therapeutic strategy to modulate cell activation
BACKGROUND: Leukotriene B(4 )(LTB(4)) is a potent inflammatory mediator that also stimulates the immune response. In addition, it promotes polymorphonuclear leukocyte phagocytosis, chemotaxis, chemokinesis and modulates cytokines release. Regarding chemical instability of the leukotriene molecule, i...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2483258/ https://www.ncbi.nlm.nih.gov/pubmed/18627613 http://dx.doi.org/10.1186/1471-2172-9-36 |
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author | Nicolete, Roberto Rius, Cristina Piqueras, Laura Jose, Peter J Sorgi, Carlos A Soares, Edson G Sanz, Maria J Faccioli, Lúcia H |
author_facet | Nicolete, Roberto Rius, Cristina Piqueras, Laura Jose, Peter J Sorgi, Carlos A Soares, Edson G Sanz, Maria J Faccioli, Lúcia H |
author_sort | Nicolete, Roberto |
collection | PubMed |
description | BACKGROUND: Leukotriene B(4 )(LTB(4)) is a potent inflammatory mediator that also stimulates the immune response. In addition, it promotes polymorphonuclear leukocyte phagocytosis, chemotaxis, chemokinesis and modulates cytokines release. Regarding chemical instability of the leukotriene molecule, in the present study we assessed the immunomodulatory activities conferred by LTB(4 )released from microspheres (MS). A previous oil-in-water emulsion solvent extraction-evaporation method was chosen to prepare LTB(4)-loaded MS. RESULTS: In the mice cremasteric microcirculation, intraescrotal injection of 0.1 ml of LTB(4)-loaded MS provoked significant increases in leukocyte rolling flux, adhesion and emigration besides significant decreases in the leukocyte rolling velocity. LTB(4)-loaded MS also increase peroxisome proliferator-activated receptor-α (PPARα) expression by murine peritoneal macrophages and stimulate them to generate nitrite levels. Monocyte chemoattractant protein-1 (MCP-1) and nitric oxide (NO) productions were also increased when human umbilical vein and artery endothelial cells (HUVECs and HUAECs, respectively) were stimulated with LTB(4)-loaded MS. CONCLUSION: LTB(4)-loaded MS preserve the biological activity of the encapsulated mediator indicating their use as a new strategy to modulate cell activation, especially in the innate immune response. |
format | Text |
id | pubmed-2483258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24832582008-07-24 Leukotriene B(4)-loaded microspheres: a new therapeutic strategy to modulate cell activation Nicolete, Roberto Rius, Cristina Piqueras, Laura Jose, Peter J Sorgi, Carlos A Soares, Edson G Sanz, Maria J Faccioli, Lúcia H BMC Immunol Research Article BACKGROUND: Leukotriene B(4 )(LTB(4)) is a potent inflammatory mediator that also stimulates the immune response. In addition, it promotes polymorphonuclear leukocyte phagocytosis, chemotaxis, chemokinesis and modulates cytokines release. Regarding chemical instability of the leukotriene molecule, in the present study we assessed the immunomodulatory activities conferred by LTB(4 )released from microspheres (MS). A previous oil-in-water emulsion solvent extraction-evaporation method was chosen to prepare LTB(4)-loaded MS. RESULTS: In the mice cremasteric microcirculation, intraescrotal injection of 0.1 ml of LTB(4)-loaded MS provoked significant increases in leukocyte rolling flux, adhesion and emigration besides significant decreases in the leukocyte rolling velocity. LTB(4)-loaded MS also increase peroxisome proliferator-activated receptor-α (PPARα) expression by murine peritoneal macrophages and stimulate them to generate nitrite levels. Monocyte chemoattractant protein-1 (MCP-1) and nitric oxide (NO) productions were also increased when human umbilical vein and artery endothelial cells (HUVECs and HUAECs, respectively) were stimulated with LTB(4)-loaded MS. CONCLUSION: LTB(4)-loaded MS preserve the biological activity of the encapsulated mediator indicating their use as a new strategy to modulate cell activation, especially in the innate immune response. BioMed Central 2008-07-15 /pmc/articles/PMC2483258/ /pubmed/18627613 http://dx.doi.org/10.1186/1471-2172-9-36 Text en Copyright © 2008 Nicolete 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 Article Nicolete, Roberto Rius, Cristina Piqueras, Laura Jose, Peter J Sorgi, Carlos A Soares, Edson G Sanz, Maria J Faccioli, Lúcia H Leukotriene B(4)-loaded microspheres: a new therapeutic strategy to modulate cell activation |
title | Leukotriene B(4)-loaded microspheres: a new therapeutic strategy to modulate cell activation |
title_full | Leukotriene B(4)-loaded microspheres: a new therapeutic strategy to modulate cell activation |
title_fullStr | Leukotriene B(4)-loaded microspheres: a new therapeutic strategy to modulate cell activation |
title_full_unstemmed | Leukotriene B(4)-loaded microspheres: a new therapeutic strategy to modulate cell activation |
title_short | Leukotriene B(4)-loaded microspheres: a new therapeutic strategy to modulate cell activation |
title_sort | leukotriene b(4)-loaded microspheres: a new therapeutic strategy to modulate cell activation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2483258/ https://www.ncbi.nlm.nih.gov/pubmed/18627613 http://dx.doi.org/10.1186/1471-2172-9-36 |
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