A POTENTIAL ROLE FOR APOPTOSIS IN NEURODEGENERATION AND ALZHEIMERS-DISEASE

被引:387
作者
COTMAN, CW
ANDERSON, AJ
机构
[1] Irvine Research Unit in Brain Aging, 1305 Biological Sciences II, Department of Psychobiology, University of California, Irvine, CA
关键词
PROGRAMMED CELL DEATH; IMMEDIATE EARLY GENE; PROTOONCOGENE; C-JUN; C-FOS; PLAQUES; NEUROFIBRILLARY TANGLES; DNA FRAGMENTATION; OXIDATIVE INJURY;
D O I
10.1007/BF02740836
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous studies have shown that beta-amyloid (A beta) peptides are neurotoxic. Recent data suggest that neurons undergoing A beta-induced cell death exhibit characteristics that correspond to the classical features of apoptosis, suggesting that these cells may initiate a program of cell death. This chapter explores the criteria and precautions that must be applied to evaluate mechanisms of cell death in vitro and in vivo, discusses the evidence supporting an apoptotic mechanism of cell death in response to A beta in cultured neurons, and describes potential correlations for these findings in the Alzheimer's disease brain. In addition, cellular signaling pathways that may be associated with apoptosis in response to A beta are examined, and support for apoptosis as a mechanism of cell death for other neurodegeneration-inducing stimuli (e.g., oxidative injury) is described. The connection of multiple stimuli that induce neuronal cell death to an apoptotic mechanism suggests that apoptosis could play a central role in neurodegeneration in the brain.
引用
收藏
页码:19 / 45
页数:27
相关论文
共 216 条
  • [1] REDOX REGULATION OF FOS AND JUN DNA-BINDING ACTIVITY INVITRO
    ABATE, C
    PATEL, L
    RAUSCHER, FJ
    CURRAN, T
    [J]. SCIENCE, 1990, 249 (4973) : 1157 - 1161
  • [2] EXPRESSION AND PURIFICATION OF THE LEUCINE ZIPPER AND DNA-BINDING DOMAINS OF FOS AND JUN - BOTH FOS AND JUN CONTACT DNA DIRECTLY
    ABATE, C
    LUK, D
    GENTZ, R
    RAUSCHER, FJ
    CURRAN, T
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (03) : 1032 - 1036
  • [3] ALNEMRI ES, 1990, J BIOL CHEM, V265, P17323
  • [4] OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING
    AMES, BN
    SHIGENAGA, MK
    HAGEN, TM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) : 7915 - 7922
  • [5] ANDERSON A, UNPUB NEUROSCIENCE
  • [6] INCREASED IMMUNOREACTIVITY FOR JUN-RELATED AND FOS-RELATED PROTEINS IN ALZHEIMERS-DISEASE - ASSOCIATION WITH PATHOLOGY
    ANDERSON, AJ
    CUMMINGS, BJ
    COTMAN, CW
    [J]. EXPERIMENTAL NEUROLOGY, 1994, 125 (02) : 286 - 295
  • [7] ONCOGENE JUN ENCODES A SEQUENCE-SPECIFIC TRANS-ACTIVATOR SIMILAR TO AP-1
    ANGEL, P
    ALLEGRETTO, EA
    OKINO, ST
    HATTORI, K
    BOYLE, WJ
    HUNTER, T
    KARIN, M
    [J]. NATURE, 1988, 332 (6160) : 166 - 171
  • [8] ARENDS MJ, 1991, INT REV EXP PATHOL, V32, P223
  • [9] GIANT MULTILEVEL CATION CHANNELS FORMED BY ALZHEIMER-DISEASE AMYLOID BETA-PROTEIN [A-BETA-P-(1-40)] IN BILAYER-MEMBRANES
    ARISPE, N
    POLLARD, HB
    ROJAS, E
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (22) : 10573 - 10577
  • [10] ALZHEIMER-DISEASE AMYLOID BETA-PROTEIN FORMS CALCIUM CHANNELS IN BILAYER-MEMBRANES - BLOCKADE BY TROMETHAMINE AND ALUMINUM
    ARISPE, N
    ROJAS, E
    POLLARD, HB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) : 567 - 571