Akt1 regulates a JNK scaffold during excitotoxic apoptosis

Neuron. 2002 Aug 15;35(4):697-709. doi: 10.1016/s0896-6273(02)00821-8.

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Animals
  • Apoptosis / drug effects
  • Apoptosis / genetics*
  • Arabidopsis Proteins*
  • Carrier Proteins / drug effects
  • Carrier Proteins / metabolism*
  • Cell Survival / drug effects
  • Cell Survival / genetics
  • Cells, Cultured
  • Central Nervous System Diseases / metabolism*
  • Central Nervous System Diseases / pathology
  • Central Nervous System Diseases / physiopathology
  • Fetus
  • Gene Deletion
  • Gene Expression / drug effects
  • Gene Expression / genetics
  • Glutamic Acid / metabolism
  • Hippocampus / cytology
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Humans
  • JNK Mitogen-Activated Protein Kinases
  • Kainic Acid / metabolism
  • Kainic Acid / pharmacology
  • Mice
  • Mice, Knockout
  • Mitogen-Activated Protein Kinases / drug effects
  • Mitogen-Activated Protein Kinases / metabolism*
  • Neurons / drug effects
  • Neurons / metabolism*
  • Neurons / pathology
  • Neurotoxins / genetics
  • Neurotoxins / metabolism*
  • Plant Proteins / drug effects
  • Plant Proteins / genetics
  • Potassium Channels / deficiency*
  • Potassium Channels / drug effects
  • Potassium Channels / genetics
  • Protein Binding / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Glutamate / drug effects
  • Receptors, Glutamate / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • Arabidopsis Proteins
  • Carrier Proteins
  • MAPK8IP1 protein, human
  • Mapk8ip protein, mouse
  • Mapk8ip1 protein, rat
  • Neurotoxins
  • Plant Proteins
  • Potassium Channels
  • Receptors, Glutamate
  • AKT1 protein, Arabidopsis
  • Glutamic Acid
  • JNK Mitogen-Activated Protein Kinases
  • Mitogen-Activated Protein Kinases
  • Kainic Acid