High level calcineurin activity predisposes neuronal cells to apoptosis

被引:140
作者
Asai, A
Qiu, JH
Narita, Y
Chi, S
Saito, N
Shinoura, N
Hamada, H
Kuchino, Y
Kirino, T
机构
[1] Univ Tokyo, Fac Med, Dept Neurosurg, Lab Neurosci & Neurooncol,Bunkyo Ku, Tokyo 1138655, Japan
[2] Inst Canc, Ctr Canc Chemotherapy, Dept Mol Biotherapy Res, Toshima Ku, Tokyo 1708455, Japan
[3] Natl Canc Ctr, Res Inst, Div Biophys, Chuo Ku, Tokyo 1040045, Japan
[4] Japan Sci & Technol Corp, CREST, Kawaguchi 3320012, Japan
关键词
D O I
10.1074/jbc.274.48.34450
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Calcineurin is a Ca2+/calmodulin-dependent protein phosphatase that is abundantly expressed in several specific areas of the brain, which are exceptionally vulnerable to stroke, epilepsy, and neurodegenerative diseases. In this study, we assessed the effects of high level activity of calcineurin on neuronal cells. Virus-mediated high level constitutive activity of calcineurin rendered neuronal cells susceptible to apoptosis induced by serum reduction or by a brief exposure to calcium ionophore. Adenovirus-mediated, high level forced activity of calcineurin induced cytochrome c/caspase-3-dependent apoptosis in neurons. Preincubation with the calcineurin inhibitors cyclosporin A and FK506 reduced susceptibility to apoptosis. High level constitutive expression of Bcl-2 or CrmA or incubation with a specific caspase-3 inhibitor inhibited the calcineurin-induced apoptosis. These data indicate that high level constitutive activity of calcineurin predisposes neuronal cells to cytochrome c/caspase-3 dependent apoptosis even under sublethal conditions.
引用
收藏
页码:34450 / 34458
页数:9
相关论文
共 57 条
  • [1] DO NMDA ANTAGONISTS PREVENT NEURONAL INJURY - YES
    ALBERS, GW
    GOLDBERG, MP
    CHOI, DW
    [J]. ARCHIVES OF NEUROLOGY, 1992, 49 (04) : 418 - 420
  • [2] Calcineurin and mitochondrial function in glutamate-induced neuronal cell death
    Ankarcrona, M
    Dypbukt, JM
    Orrenius, S
    Nicotera, P
    [J]. FEBS LETTERS, 1996, 394 (03): : 321 - 324
  • [3] CELL-AUTONOMOUS FAS (CD95) FAS-LIGAND INTERACTION MEDIATES ACTIVATION-INDUCED APOPTOSIS IN T-CELL HYBRIDOMAS
    BRUNNER, T
    MOGIL, RJ
    LAFACE, D
    YOO, NJ
    MAHBOUBI, A
    ECHEVERRI, F
    MARTIN, SJ
    FORCE, WR
    LYNCH, DH
    WARE, CF
    GREEN, DR
    [J]. NATURE, 1995, 373 (6513) : 441 - 444
  • [4] CHOI DW, 1987, J NEUROSCI, V7, P369
  • [5] CRAIN BJ, 1988, NEUROSCIENCE, V27, P387
  • [6] IMMUNOSUPPRESSANT FK506 ENHANCES PHOSPHORYLATION OF NITRIC-OXIDE SYNTHASE AND PROTECTS AGAINST GLUTAMATE NEUROTOXICITY
    DAWSON, TM
    STEINER, JP
    DAWSON, VL
    DINERMAN, JL
    UHL, GR
    SNYDER, SH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (21) : 9808 - 9812
  • [7] AUTOCRINE T-CELL SUICIDE MEDIATED BY APO-1/(FAS/CD95)
    DHEIN, J
    WALCZAK, H
    BAUMLER, C
    DEBATIN, KM
    KRAMMER, PH
    [J]. NATURE, 1995, 373 (6513) : 438 - 441
  • [8] REGULATION OF MICROTUBULE ASSOCIATED PROTEIN-2 (MAP2) EXPRESSION BY NERVE GROWTH-FACTOR IN PC12 CELLS
    FISCHER, I
    RICHTERLANDSBERG, C
    SAFAEI, R
    [J]. EXPERIMENTAL CELL RESEARCH, 1991, 194 (02) : 195 - 201
  • [9] FREUND TF, 1990, EXP BRAIN RES, V83, P55
  • [10] FRUMAN DA, 1992, P NATL ACAD SCI USA, V89, P3689