Transglutaminase activity is increased in Alzheimer's disease brain

被引:164
作者
Johnson, GVW
Cox, TM
Lockhart, JP
Zinnerman, MD
Miller, ML
Powers, RE
机构
[1] Dept. Psychiat. and Behav. Neurbio., SC1061, University of Alabama at Birmingham, Birmingham
关键词
transglutaminase; neurofibrillary tangle; Alzheimer's disease; tau protein;
D O I
10.1016/S0006-8993(96)01431-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Transglutaminase is a calcium-activated enzyme that crosslinks substrate proteins into insoluble, often filamentous aggregates resistant to proteases. Because the neurofibrillary tangles in Alzheimer's disease have similar characteristics, and because tau protein, the major component of these tangles is an excellent substrate of transglutaminase in vitro, transglutaminase activity and levels were measured in control and Alzheimer's disease brain. Frozen prefrontal cortex and cerebellum samples from Alzheimer's disease and control cases matched for age and postmortem interval were used in the analyses. Total transglutaminase activity was significantly higher in the Alzheimer's disease prefrontal cortex compared to control. In addition the levels of tissue transglutaminase, as determined by quantitative immunoblotting, were elevated approximately 3-fold in Alzheimer's disease prefrontal cortex compared to control. To our knowledge, this is the first demonstration that transglutaminase is increased in Alzheimer's disease brain. There were no significant differences in transglutaminase activity or levels in the cerebellum between control and Alzheimer's disease cases. Because the elevation of transglutaminase in the Alzheimer's disease samples occurred in the prefrontal cortex, where neurofibrillary pathology is usually abundant, and not in the cerebellum, which is usually spared in Alzheimer's disease, it can be suggested that transglutaminase could be a contributing factor in neurofibrillary tangle formation.
引用
收藏
页码:323 / 329
页数:7
相关论文
共 55 条
  • [41] MATTSON MP, 1994, ANN NY ACAD SCI, V747, P50
  • [42] MILLER CCJ, 1986, J NEUROCHEM, V46, P1912
  • [43] MILLER ML, 1995, J NEUROCHEM, V65, P1760
  • [44] PROLINE-DIRECTED AND NON-PROLINE-DIRECTED PHOSPHORYLATION OF PHF-TAU
    MORISHIMAKAWASHIMA, M
    HASEGAWA, M
    TAKIO, K
    SUZUKI, M
    YOSHIDA, H
    TITANI, K
    IHARA, Y
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (02) : 823 - 829
  • [45] G(H) - A GTP-BINDING PROTEIN WITH TRANSGLUTAMINASE ACTIVITY AND RECEPTOR SIGNALING FUNCTION
    NAKAOKA, H
    PEREZ, DM
    BAEK, KJ
    DAS, T
    HUSAIN, A
    MISONO, K
    IM, MJ
    GRAHAM, RM
    [J]. SCIENCE, 1994, 264 (5165) : 1593 - 1596
  • [46] PURIFICATION AND CHARACTERIZATION OF RAT-BRAIN TRANSGLUTAMINASE
    OHASHI, H
    ITOH, Y
    BIRCKBICHLER, PJ
    TAKEUCHI, Y
    [J]. JOURNAL OF BIOCHEMISTRY, 1995, 118 (06) : 1271 - 1278
  • [47] A ROLE FOR TRANSGLUTAMINASE IN NEUROTRANSMITTER RELEASE BY RAT-BRAIN SYNAPTOSOMES
    PASTUSZKO, A
    WILSON, DF
    ERECINSKA, M
    [J]. JOURNAL OF NEUROCHEMISTRY, 1986, 46 (02) : 499 - 508
  • [48] TRANSGLUTAMINASE-C IN CEREBELLAR GRANULE NEURONS - REGULATION AND LOCALIZATION OF SUBSTRATE CROSS-LINKING
    PERRY, MJM
    MAHONEY, SA
    HAYNES, LW
    [J]. NEUROSCIENCE, 1995, 65 (04) : 1063 - 1076
  • [49] OXIDATION OF CYSTEINE-322 IN THE REPEAT DOMAIN OF MICROTUBULE-ASSOCIATED PROTEIN-TAU CONTROLS THE IN-VITRO ASSEMBLY OF PAIRED HELICAL FILAMENTS
    SCHWEERS, O
    MANDELKOW, EM
    BIERNAT, J
    MANDELKOW, E
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) : 8463 - 8467
  • [50] ALZHEIMERS-DISEASE - INSOLUBILITY OF PARTIALLY PURIFIED PAIRED HELICAL FILAMENTS IN SODIUM DODECYL-SULFATE AND UREA
    SELKOE, DJ
    IHARA, Y
    SALAZAR, FJ
    [J]. SCIENCE, 1982, 215 (4537) : 1243 - 1245