Involvement of ASK1 in Ca2+-induced p38 MAP kinase activation.

نویسندگان

  • Kohsuke Takeda
  • Atsushi Matsuzawa
  • Hideki Nishitoh
  • Kei Tobiume
  • Satoshi Kishida
  • Jun Ninomiya-Tsuji
  • Kunihiro Matsumoto
  • Hidenori Ichijo
چکیده

The mammalian mitogen-activated protein (MAP) kinase kinase kinase apoptosis signal-regulating kinase 1 (ASK1) is a pivotal component in cytokine- and stress-induced apoptosis. It also regulates cell differentiation and survival through p38 MAP kinase activation. Here we show that Ca2+ signalling regulates the ASK1-p38 MAP kinase cascade. Ca2+ influx evoked by membrane depolarization in primary neurons and synaptosomes induced activation of p38, which was impaired in those derived from ASK1-deficient mice. Ca2+/calmodulin-dependent protein kinase type II (CaMKII) activated ASK1 by phosphorylation. Moreover, p38 activation induced by the expression of constitutively active CaMKII required endogenous ASK1. Thus, ASK1 is a critical intermediate of Ca2+ signalling between CaMKII and p38 MAP kinase.

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عنوان ژورنال:
  • EMBO reports

دوره 5 2  شماره 

صفحات  -

تاریخ انتشار 2004