Suppressive effects of dehydrocostus lactone on the toll-like receptor signaling pathways

Int Immunopharmacol. 2020 Jan:78:106075. doi: 10.1016/j.intimp.2019.106075. Epub 2019 Dec 5.

Abstract

Toll-like receptors (TLRs) are a group of pattern-recognition receptors (PRRs) that are at the core of innate and adaptive immune responses. TLRs activation triggers the activation of two downstream signaling pathways, the myeloid differential factor 88 (MyD88)- and toll-interleukin-1 receptor domain-containing adapter inducing interferon-β (TRIF)-dependent pathways. To evaluate the therapeutic potential of DHL, a natural sesquiterpene lactone derived from Inulahelenium L. and Saussurea lappa, we examined its effect on signal transduction via the TLR signaling pathways. DHL inhibited the activation of nuclear factor-κB (NF-κB) and interferon regulatory factor 3 (IRF3), the representative transcription factors involved in the inflammatory response, induced by TLR agonists, as well as the expression of cyclooxygenase-2 and interferon inducible protein-10. DHL also inhibited the activation of NF-κB and IRF3 induced by the overexpression of downstream signaling components of the TLRs signaling pathways. All results suggest that DHL might become a new therapeutic drug for a variety of inflammatory diseases.

Keywords: Dehydrocostus lactone; IRF3; MyD88; TRIF; Toll-like receptor.

MeSH terms

  • Adaptor Proteins, Vesicular Transport / metabolism
  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Anti-Inflammatory Agents / therapeutic use
  • HEK293 Cells
  • Humans
  • Inflammation / drug therapy*
  • Inflammation / immunology
  • Interferon Regulatory Factor-3 / metabolism
  • Inula / chemistry
  • Lactones / pharmacology*
  • Lactones / therapeutic use
  • Mice
  • Myeloid Differentiation Factor 88 / immunology
  • Myeloid Differentiation Factor 88 / metabolism
  • NF-kappa B / metabolism
  • RAW 264.7 Cells
  • Saussurea / chemistry
  • Sesquiterpenes / pharmacology*
  • Sesquiterpenes / therapeutic use
  • Signal Transduction / drug effects*
  • Signal Transduction / immunology
  • Toll-Like Receptors / metabolism*

Substances

  • Adaptor Proteins, Vesicular Transport
  • Anti-Inflammatory Agents
  • Interferon Regulatory Factor-3
  • Lactones
  • Myeloid Differentiation Factor 88
  • NF-kappa B
  • Sesquiterpenes
  • TICAM-1 protein, mouse
  • TICAM1 protein, human
  • Toll-Like Receptors
  • dehydrocostus lactone