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
  • [1] Transduction of interleukin-2 antiapoptotic and proliferative signals via Akt protein kinase
    Ahmed, NN
    Grimes, HL
    Bellacosa, A
    Chan, TO
    Tsichlis, PN
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) : 3627 - 3632
  • [2] Amino-terminal phosphorylation of c-Jun regulates stress-induced apoptosis and cellular proliferation
    Behrens, A
    Sibilia, M
    Wagner, EF
    [J]. NATURE GENETICS, 1999, 21 (03) : 326 - 329
  • [3] Akt activation by growth factors is a multiple-step process: the role of the PH domain
    Bellacosa, A
    Chan, TO
    Ahmed, NN
    Datta, K
    Malstrom, S
    Stokoe, D
    McCormick, F
    Feng, JN
    Tsichlis, P
    [J]. ONCOGENE, 1998, 17 (03) : 313 - 325
  • [4] Cdc42-induced activation of the mixed-lineage kinase SPRK in vivo -: Requirement of the Cdc42/Rac interactive binding motif and changes in phosphorylation
    Böck, BC
    Vacratsis, PO
    Qamirani, E
    Gallo, KA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (19) : 14231 - 14241
  • [5] IB1, a JIP-1-related nuclear protein present in insulin-secreting cells
    Bonny, C
    Nicod, P
    Waeber, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (04) : 1843 - 1846
  • [6] Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor
    Brunet, A
    Bonni, A
    Zigmond, MJ
    Lin, MZ
    Juo, P
    Hu, LS
    Anderson, MJ
    Arden, KC
    Blenis, J
    Greenberg, ME
    [J]. CELL, 1999, 96 (06) : 857 - 868
  • [7] Regulation of cell death protease caspase-9 by phosphorylation
    Cardone, MH
    Roy, N
    Stennicke, HR
    Salvesen, GS
    Franke, TF
    Stanbridge, E
    Frisch, S
    Reed, JC
    [J]. SCIENCE, 1998, 282 (5392) : 1318 - 1321
  • [8] Role of Akt and c-Jun N-terminal kinase 2 in apoptosis induced by interleukin-4 deprivation
    Cerezo, A
    Martínez, C
    Lanzarot, D
    Fischer, S
    Franke, TF
    Rebollo, A
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (11) : 3107 - 3118
  • [9] Synergistic interaction of MEK kinase 2, c-Jun N-terminal kinase (JNK) kinase 2, and JNK1 results in efficient and specific JNK1 activation
    Cheng, JK
    Yang, JH
    Xia, Y
    Karin, M
    Su, B
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (07) : 2334 - 2342
  • [10] AKT2, A PUTATIVE ONCOGENE ENCODING A MEMBER OF A SUBFAMILY OF PROTEIN-SERINE THREONINE KINASES, IS AMPLIFIED IN HUMAN OVARIAN CARCINOMAS
    CHENG, JQ
    GODWIN, AK
    BELLACOSA, A
    TAGUCHI, T
    FRANKE, TF
    HAMILTON, TC
    TSICHLIS, PN
    TESTA, JR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (19) : 9267 - 9271