Document Detail


Differential regulation of Toll-like receptor signalling in spleen and Peyer's patch dendritic cells.
MedLine Citation:
PMID:  20545785     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Toll-like receptor (TLR) signalling shapes dendritic cell (DC) responses by inducing co-stimulatory molecule up-regulation and cytokine secretion while TLR regulatory proteins inhibit this process. We aimed to determine if gene expression of TLRs and TLR regulatory proteins underpins the functionally different lipopolysaccharide (LPS) responses of DCs from murine Peyer's patches (PP) and spleen and of murine bacteria-conditioned bone-marrow-derived cells. Isolated spleen and PP DCs were analysed for basal expression of TLRs by flow cytometry and real time quantitative reverse transcription polymerase chain reaction (qRT-PCR). The DCs were stimulated with LPS to determine cytokine secretion by enzyme-linked immunosorbent assay and expression of TLR regulatory proteins by qRT-PCR. In vitro results were confirmed following in vivo intraperitoneal LPS injection. In addition, changes in gene expression of TLR regulatory proteins were assessed in bacteria-conditioned bone-marrow-derived cells. Results indicated that surface expression of TLR2 and TLR4 on PP DCs was decreased compared with spleen DCs. The PP DCs secreted a limited profile of cytokines compared with spleen DCs following LPS stimulation. In vivo LPS exposure up-regulated sigirr, tollip and tmed1 messenger RNA in PP DCs, but not spleen DCs. Similar gene expression changes were observed in bacteria-conditioned bone-marrow-derived cells. Therefore, functionally different LPS responses in PP and spleen DCs reflect their characteristic expression of TLRs and TLR regulatory proteins. Differential regulation of TLR signalling was also evident in bacteria-conditioned bone-marrow-derived cells indicating that bacterial signalling may be a mechanism for inducing altered gene regulation in PP DCs.
Authors:
Julie M Davies; John MacSharry; Fergus Shanahan
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Immunology     Volume:  131     ISSN:  1365-2567     ISO Abbreviation:  Immunology     Publication Date:  2010 Nov 
Date Detail:
Created Date:  2010-11-02     Completed Date:  2011-02-02     Revised Date:  2011-11-01    
Medline Journal Info:
Nlm Unique ID:  0374672     Medline TA:  Immunology     Country:  England    
Other Details:
Languages:  eng     Pagination:  438-48     Citation Subset:  IM    
Copyright Information:
© 2010 The Authors. Immunology © 2010 Blackwell Publishing Ltd.
Affiliation:
Alimentary Pharmabiotic Centre, National University of Ireland, University College Cork, Cork, Ireland. juliemariedavies@hotmail.com
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MeSH Terms
Descriptor/Qualifier:
Animals
Bifidobacteriales Infections / immunology*
Bifidobacterium / immunology*,  pathogenicity
Bone Marrow Cells / immunology,  metabolism*,  microbiology,  pathology
Cells, Cultured
Cytokines / secretion
Dendritic Cells / immunology,  metabolism*,  pathology
Gene Expression Regulation
Intracellular Signaling Peptides and Proteins / genetics,  metabolism
Lipopolysaccharides / immunology
Mice
Mice, Inbred BALB C
Peyer's Patches / pathology*
Receptors, Interleukin-1 / genetics,  metabolism
Signal Transduction
Spleen / pathology*
Toll-Like Receptor 2 / immunology,  metabolism*
Toll-Like Receptor 4 / immunology,  metabolism*
Chemical
Reg. No./Substance:
0/Cytokines; 0/Intracellular Signaling Peptides and Proteins; 0/Lipopolysaccharides; 0/Receptors, Interleukin-1; 0/Tir8 protein, mouse; 0/Tlr2 protein, mouse; 0/Tlr4 protein, mouse; 0/Toll-Like Receptor 2; 0/Toll-Like Receptor 4; 0/Tollip protein, mouse

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