Publication | Open Access
Activation of Toll-Like Receptor 2 (TLR2) and TLR4/MD2 by <i>Neisseria</i> Is Independent of Capsule and Lipooligosaccharide (LOS) Sialylation but Varies Widely among LOS from Different Strains
73
Citations
50
References
2003
Year
Microbial PathogensTruncated LosInnate Immune SystemImmunologyPathologyCapsular PolysaccharideInnate ImmunityImmune SystemToll-like Receptor 2InflammationToll-like ReceptorsDifferent StrainsVaries WidelyImmunopathologyHost-pathogen InteractionsProinflammatory ResponsesAutoimmunityImmune FunctionHost-microbe InteractionClinical MicrobiologyPhagocyteCytokineMolecular ImmunologyPathogenesisMicrobiologyMedicineViral Immunity
Lipooligosaccharide (LOS) structure and capsular polysaccharide of Neisseria meningitidis each greatly influence the virulence of the organism and the quality of host innate immune responses. In this study, we found that production of the proinflammatory cytokine tumor necrosis factor (TNF) by a human monocyte-derived cell line (THP-1) exposed to strains of N. meningitidis lacking capsule and/or with truncated LOS was similar to that elicited by the isogenic wild-type strain. These mutants also exhibited no difference in induction of the interleukin-8 (IL-8) promoter in a transfected HeLa cell system of Toll-like receptor 2 (TLR2) and TLR4/MD2 signaling. However, purified LOS from diverse strains of Neisseria (both N. meningitidis and N. gonorrhoeae) caused widely variant levels of IL-8 promoter induction in cells expressing MD2 that correlated with the production of TNF from THP-1 cells. These data suggest that although modification of the oligosaccharide chain of LOS and/or absence of capsule do not affect cell signaling mediated by TLR4/MD2, fine-structural differences in the LOS do influence signaling through TLR4/MD2 and, through this pathway, influence some of the proinflammatory responses elicited by Neisseria.
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