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Serine lipids of Porphyromonas gingivalis are human and mouse Toll-like receptor 2 ligands.

Authors :
Clark RB
Cervantes JL
Maciejewski MW
Farrokhi V
Nemati R
Yao X
Anstadt E
Fujiwara M
Wright KT
Riddle C
La Vake CJ
Salazar JC
Finegold S
Nichols FC
Source :
Infection and immunity [Infect Immun] 2013 Sep; Vol. 81 (9), pp. 3479-89. Date of Electronic Publication: 2013 Jul 08.
Publication Year :
2013

Abstract

The total cellular lipids of Porphyromas gingivalis, a known periodontal pathogen, were previously shown to promote dendritic cell activation and inhibition of osteoblasts through engagement of Toll-like receptor 2 (TLR2). The purpose of the present investigation was to fractionate all lipids of P. gingivalis and define which lipid classes account for the TLR2 engagement, based on both in vitro human cell assays and in vivo studies in mice. Specific serine-containing lipids of P. gingivalis, called lipid 654 and lipid 430, were identified in specific high-performance liquid chromatography fractions as the TLR2-activating lipids. The structures of these lipids were defined using tandem mass spectrometry and nuclear magnetic resonance methods. In vitro, both lipid 654 and lipid 430 activated TLR2-expressing HEK cells, and this activation was inhibited by anti-TLR2 antibody. In contrast, TLR4-expressing HEK cells failed to be activated by either lipid 654 or lipid 430. Wild-type (WT) or TLR2-deficient (TLR2(-/-)) mice were injected with either lipid 654 or lipid 430, and the effects on serum levels of the chemokine CCL2 were measured 4 h later. Administration of either lipid 654 or lipid 430 to WT mice resulted in a significant increase in serum CCL2 levels; in contrast, the administration of lipid 654 or lipid 430 to TLR2(-/-) mice resulted in no increase in serum CCL2. These results thus identify a new class of TLR2 ligands that are produced by P. gingivalis that likely play a significant role in mediating inflammatory responses both at periodontal sites and, potentially, in other tissues where these lipids might accumulate.

Details

Language :
English
ISSN :
1098-5522
Volume :
81
Issue :
9
Database :
MEDLINE
Journal :
Infection and immunity
Publication Type :
Academic Journal
Accession number :
23836823
Full Text :
https://doi.org/10.1128/IAI.00803-13