Human platelets can discriminate between various bacterial LPS isoforms via TLR4 signaling and differential cytokine secretion

Copyright © 2012 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 145(2012), 3 vom: 14. Dez., Seite 189-200
1. Verfasser: Berthet, Julien (VerfasserIn)
Weitere Verfasser: Damien, Pauline, Hamzeh-Cognasse, Hind, Arthaud, Charles-Antoine, Eyraud, Marie-Ange, Zéni, Fabrice, Pozzetto, Bruno, McNicol, Archibald, Garraud, Olivier, Cognasse, Fabrice
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2012
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Comparative Study Journal Article Research Support, Non-U.S. Gov't CD63 protein, human CXCL8 protein, human Cytokines IL6 protein, human Interleukin-6 Interleukin-8 Lipopolysaccharide Receptors mehr... Lipopolysaccharides P-Selectin Protein Isoforms SELP protein, human TLR4 protein, human Tetraspanin 30 Toll-Like Receptor 4 Tumor Necrosis Factor-alpha
Beschreibung
Zusammenfassung:Copyright © 2012 Elsevier Inc. All rights reserved.
Platelets are currently acknowledged as cells of innate immunity and inflammation and play a complex role in sepsis. We examined whether different types of LPS have different effects on the release of soluble signaling/effective molecules from platelets. We used platelet-rich plasma from healthy volunteers and LPS from two strains of gram-negative bacteria with disparate LPS structures. We combined LPS-stimulated platelet supernatants with reporter cells and measured the PBMC cytokine secretion profiles. Upon stimulation of platelets with both Escherichia coli O111 and Salmonella minnesota LPS, the platelet LPS::TLR4 interaction activated pathways to trigger the production of a large number of molecules. The different platelet supernatants caused differential PBMC secretion of IL-6, TNFα, and IL-8. Our data demonstrate that platelets have the capacity to sense external signals differentially through a single type of pathogen recognition receptor and adjust the innate immune response appropriately for pathogens exhibiting different types of 'danger' signals
Beschreibung:Date Completed 17.01.2013
Date Revised 16.08.2019
published: Print-Electronic
CommentIn: Clin Immunol. 2013 Jan;146(1):13-4. - PMID 23168607
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2012.09.004