Akt1 Regulates a JNK Scaffold during Excitotoxic Apoptosis

نویسندگان

  • Albert H Kim
  • Hiroko Yano
  • Han Cho
  • Debra Meyer
  • Bob Monks
  • Ben Margolis
  • Morris J Birnbaum
  • Moses V Chao
چکیده

Cell survival is determined by a balance among signaling cascades, including those that recruit the Akt and JNK pathways. Here we describe a novel interaction between Akt1 and JNK interacting protein 1 (JIP1), a JNK pathway scaffold. Direct association between Akt1 and JIP1 was observed in primary neurons. Neuronal exposure to an excitotoxic stimulus decreased the Akt1-JIP1 interaction and concomitantly increased association between JIP1 and JNK. Akt1 interaction with JIP1 inhibited JIP1-mediated potentiation of JNK activity by decreasing JIP1 binding to specific JNK pathway kinases. Consistent with this view, neurons from Akt1-deficient mice exhibited higher susceptibility to kainate than wild-type littermates. Overexpression of Akt1 mutants that bind JIP1 reduced excitotoxic apoptosis. These results suggest that Akt1 binding to JIP1 acts as a regulatory gate preventing JNK activation, which is released under conditions of excitotoxic injury.

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عنوان ژورنال:
  • Neuron

دوره 35  شماره 

صفحات  -

تاریخ انتشار 2002