Cooperation between MyD88 and TRIF pathways in TLR synergy via IRF5 activation

Xinshou Ouyang, Hideo Negishi, Rie Takeda, Yasuyuki Fujita, Tadatsugu Taniguchi, Kenya Honda

研究成果: Article査読

95 被引用数 (Scopus)

抄録

Signaling by Toll-like receptors (TLRs) is central to evoking innate immunity, wherein each TLR is activated by distinct pathogen-derived agonists. It has been shown previously that TLR signaling occurs in synergy when certain TLR agonist combinations simultaneously activate immune cells. This synergism may constitute a mechanism critical to ensuring the effective activation of the immune system by multiple TLR activating molecules associated with a given pathogen; however, its underlying mechanism(s) remain unclarified. Here, we provide evidence that TLRs utilizing the MyD88 adaptor selectively cooperate with those utilizing the TRIF adaptor for synergistic induction of a set of target genes, and that this synergism is abrogated in cells lacking either MyD88 or TRIF. Moreover, we also provide evidence that this TLR synergy is mediated, at least in part, by activation of the transcription factor interferon regulatory factor 5 (IRF5). Thus, our findings offer a mechanistic insight into TLR synergy, revealing the hitherto unknown cross talk between the MyD88 and TRIF pathways for a robust TLR-mediated activation of the immune system.

本文言語English
ページ(範囲)1045-1051
ページ数7
ジャーナルBiochemical and Biophysical Research Communications
354
4
DOI
出版ステータスPublished - 2007 3月 23
外部発表はい

ASJC Scopus subject areas

  • 生物理学
  • 生化学
  • 分子生物学
  • 細胞生物学

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