TLR9-independent effects of inhibitory oligonucleotides on macrophage responses to S. typhimurium

Angela Trieu, Nilesh Bokil, Jasmyn A. Dunn, Tara L. Roberts, Damo Xu, Foo Y. Liew, David A. Hume, Katryn J. Stacey, Matthew J. Sweet

Research output: Contribution to journalArticlepeer-review

Abstract

Detection of bacterial CpG-containing DNA (CpG DNA) by innate immune cells is dependent on toll-like receptor 9 (TLR9). Here we show that the expression of tlr9 mRNA was induced in mouse bone marrow-derived macrophages (BMMs) upon infection with the facultative Gram-negative intracellular bacterium Salmonella enterica serovar Typhimurium (S. typhimurium). Treatment of BMM with the inhibitory oligonucleotide (ODN) 2114, an antagonist of TLR9 signalling, enhanced intracellular S. typhimurium numbers approximately fivefold, whereas a control ODN (2310) had no significant effect. Surprisingly, 2114 also amplified S. typhimurium bacterial loads in TLR9-deficient BMM. Indeed, 2114 suppressed responses (nuclear factor-kappa B-dependent reporter gene expression and interleukin-12p40 secretion) to not only CpG DNA, but also the TLR2 ligand Pam(3)Cys, in BMM and RAW264 cells in a sequence-specific manner. Inhibitory ODNs, which have been proposed as therapeutic agents for the treatment of systemic lupus erythematosus because of their inhibitory effects on TLR9 signalling, may thus compromise the host response to bacterial pathogens through TLR9-independent mechanisms.

Original languageEnglish
Pages (from-to)218-225
Number of pages8
JournalImmunology and Cell Biology
Volume87
Issue number3
DOIs
Publication statusPublished - 2009

Keywords

  • Animals
  • Cell Line
  • Macrophage Colony-Stimulating Factor/pharmacology
  • Macrophages/drug effects
  • Macrophages/immunology
  • Macrophages/microbiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Oligodeoxyribonucleotides/pharmacology
  • Salmonella Infections/immunology
  • Salmonella Infections/microbiology
  • Salmonella typhimurium/immunology
  • Toll-Like Receptor 9/antagonists & inhibitors
  • Toll-Like Receptor 9/genetics
  • Toll-Like Receptor 9/metabolism

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