| Literature DB >> 12194869 |
Albert H Kim1, Hiroko Yano, Han Cho, Debra Meyer, Bob Monks, Ben Margolis, Morris J Birnbaum, Moses V Chao.
Abstract
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.Entities:
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Year: 2002 PMID: 12194869 DOI: 10.1016/s0896-6273(02)00821-8
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173