Inhibition of homodimerization of Toll-like receptor 4 by curcumin

Hyung S. Youn, Shin I. Saitoh, Kensuke Miyake, Daniel H. Hwang

Research output: Contribution to journalArticle

166 Scopus citations

Abstract

Toll-like receptors play a key role in sensing microbial components and inducing innate immune responses. Ligand-induced dimerization of TLR4 is required for the activation of downstream signaling pathways. Thus, the receptor dimerization may be one of the first lines of regulation in activating TLR-mediated signaling pathways and induction of subsequent immune responses. LPS induces the activation of NF-κB and IRF3 through MyD88- or TRIF-dependent pathways. Curcumin, a polyphenol found in the plant Curcuma longa, has been shown to suppress the activation of NF-κB induced by various pro-inflammatory stimuli by inhibiting IKKβ kinase activity in MyD88-dependent pathway. Curcumin also inhibited LPS-induced IRF3 activation. These results imply that curcumin inhibits both MyD88- and TRIF-dependent pathways in LPS-induced TLR4 signaling. However, in TRIF-dependent pathway, curcumin did not inhibit IRF3 activation induced by overexpression of TRIF in 293T cells. These results suggest that TLR4 receptor complex is the molecular target of curcumin in addition to IKKβ. Here, we report biochemical evidence that phytochemicals (curcumin and sesquiterpene lactone) inhibit both ligand-induced and ligand-independent dimerization of TLR4. Furthermore, these results demonstrate that small molecules with non-microbial origin can directly inhibit TLRs-mediated signaling pathways at the receptor level. These results imply that the activation of TLRs and subsequent immune/inflammatory responses induced by endogenous molecules or chronic infection can be modulated by certain dietary phytochemicals we consume daily.

Original languageEnglish (US)
Pages (from-to)62-69
Number of pages8
JournalBiochemical Pharmacology
Volume72
Issue number1
DOIs
StatePublished - Jun 28 2006
Externally publishedYes

Keywords

  • Curcumin
  • LPS
  • MyD88
  • Phytochemical
  • Toll-like receptor 4
  • TRIF

ASJC Scopus subject areas

  • Pharmacology

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