Akt1 regulates a JNK scaffold during excitotoxic apoptosis

被引:180
作者
Kim, AH
Yano, H
Cho, H
Meyer, D
Monks, B
Margolis, B
Birnbaum, MJ
Chao, MV [1 ]
机构
[1] NYU, Sch Med, Mol Neurobiol Program, Skirball Inst Biomol Med, New York, NY 10016 USA
[2] Univ Michigan, Howard Hughes Med Inst, Dept Internal Med, Ann Arbor, MI 48109 USA
[3] Univ Penn, Sch Med, Howard Hughes Med Inst, Dept Internal Med, Philadelphia, PA 19104 USA
关键词
D O I
10.1016/S0896-6273(02)00821-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:697 / 709
页数:13
相关论文
共 62 条
  • [21] Regulation of neuronal survival by the serine-threonine protein kinase Akt
    Dudek, H
    Datta, SR
    Franke, TF
    Birnbaum, MJ
    Yao, RJ
    Cooper, GM
    Segal, RA
    Kaplan, DR
    Greenberg, ME
    [J]. SCIENCE, 1997, 275 (5300) : 661 - 665
  • [22] Direct inhibition of c-Jun N-terminal kinase in sympathetic neurones prevents c-jun promoter activation and NGF withdrawal-induced death
    Eilers, A
    Whitfield, J
    Shah, B
    Spadoni, C
    Desmond, H
    Ham, J
    [J]. JOURNAL OF NEUROCHEMISTRY, 2001, 76 (05) : 1439 - 1454
  • [23] Pheromone response, mating and cell biology
    Elion, EA
    [J]. CURRENT OPINION IN MICROBIOLOGY, 2000, 3 (06) : 573 - 581
  • [24] FERKANY JW, 1984, NATURE, V308, P561, DOI 10.1038/308561a0
  • [25] Direct regulation of the Akt proto-oncogene product by phosphatidylinositol-3,4-bisphosphate
    Franke, TF
    Kaplan, DR
    Cantley, LC
    Toker, A
    [J]. SCIENCE, 1997, 275 (5300) : 665 - 668
  • [26] Inhibition of JNK by overexpression of the JNK binding domain of JIP-1 prevents apoptosis in sympathetic neurons
    Harding, TC
    Xue, LZ
    Bienemann, A
    Haywood, D
    Dickens, M
    Tolkovsky, AM
    Uney, JB
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (07) : 4531 - 4534
  • [27] Hetman M, 2000, J NEUROSCI, V20, P2567
  • [28] MKK7 is a stress-activated mitogen-activated protein kinase kinase functionally related to hemipterous
    Holland, PM
    Suzanne, M
    Campbell, JS
    Noselli, S
    Cooper, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (40) : 24994 - 24998
  • [29] CLONED GLUTAMATE RECEPTORS
    HOLLMANN, M
    HEINEMANN, S
    [J]. ANNUAL REVIEW OF NEUROSCIENCE, 1994, 17 : 31 - 108
  • [30] Ito M, 1999, MOL CELL BIOL, V19, P7539