ROS-dependent activation of ASK1 in inflammatory signaling

研究成果: Review article査読

5 被引用数 (Scopus)

抄録

Reactive oxygen species (ROS) have been implicated in the regulation of signal transduction. ROS lead to a wide variety of cellular responses through the activation of various signal transduction pathways. Several protein kinases are known to be activated by ROS, and contribute to the induction of ROS-dependent cellular responses. However, the molecular mechanisms by which ROS induce the activation of these protein kinases are poorly understood. Apoptosis signal-regulating kinase 1 (ASK1) is an ROS-responsive protein kinase that belongs to the mitogen-activated protein kinase kinase kinase (MAP3K) family. The molecular mechanism of ASK1 activation induced by ROS has been well-characterized, and endogenous ASK1 constitutively forms a mega-complex that functions as a signalosome which causes the ROS-dependent activation of ASK1. On the other hand, it has been demonstrated that several inflammatory mediators such as tumor necrosis factor α (TNFα), lipopolysaccharide (LPS), and extracellular ATP (eATP) activate ASK1 in an ROS-dependent manner. Analyses of ASK1-deficient mice have revealed that the ROS-dependent activation of ASK1 plays a pivotal role in inflammatory mediator-induced cellular responses. This review describes recent studies on the molecular mechanism of ROS-dependent activation of ASK1 and its roles in inflammatory signaling.

本文言語English
ページ(範囲)107-114
ページ数8
ジャーナルjournal of oral biosciences
50
2
DOI
出版ステータスPublished - 2008 5
外部発表はい

ASJC Scopus subject areas

  • 医学(その他)
  • 生化学、遺伝学、分子生物学(全般)
  • 歯科学(全般)

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