THE ALZHEIMERS A-BETA PEPTIDE INDUCES NEURODEGENERATION AND APOPTOTIC CELL-DEATH IN TRANSGENIC MICE

被引:477
作者
LAFERLA, FM
TINKLE, BT
BIEBERICH, CJ
HAUDENSCHILD, CC
JAY, G
机构
[1] AMER RED CROSS, JEROME H HOLLAND LAB BIOMED SCI, DEPT VIROL, ROCKVILLE, MD 20855 USA
[2] AMER RED CROSS, JEROME H HOLLAND LAB BIOMED SCI, DEPT EXPTL PATHOL, ROCKVILLE, MD 20855 USA
关键词
D O I
10.1038/ng0195-21
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To test whether the hypothesis that the Alzheimer's A beta peptide is neurotoxic, we introduced a transgene into mice to direct expression of this peptide to neurons. We show that the transgene is expressed in brain regions which are severely affected in Alzheimer's disease resulting in extensive neuronal degeneration. Morphological and biochemical evidence indicates that the eventual death of these cells occurs by apoptosis. Coincident with the cell degeneration and cell death is the presence of a striking reactive gliosis. Over 50% of the transgenic mice die by 12 months of age, half the normal life span of control mice. These data show that A beta is neurotoxic in vivo and suggest that apoptosis may be responsible for the accompanying neuronal loss, the principal underlying cellular feature of Alzheimer's disease.
引用
收藏
页码:21 / 30
页数:10
相关论文
共 69 条
[1]   EXPRESSION OF CHICKEN LIVER-CELL ADHESION MOLECULE FUSION GENES IN TRANSGENIC MICE [J].
BEGEMANN, M ;
TAN, SS ;
CUNNINGHAM, BA ;
EDELMAN, GM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (22) :9042-9046
[2]   GENERATION OF BETA-AMYLOID IN THE SECRETORY PATHWAY IN NEURONAL AND NONNEURONAL CELLS [J].
BUSCIGLIO, J ;
GABUZDA, DH ;
MATSUDAIRA, P ;
YANKNER, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :2092-2096
[3]   MULTIPLEX GENE-REGULATION - A 2-TIERED APPROACH TO TRANSGENE REGULATION IN TRANSGENIC MICE [J].
BYRNE, GW ;
RUDDLE, FH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (14) :5473-5477
[4]   RELEASE OF EXCESS AMYLOID BETA-PROTEIN FROM A MUTANT AMYLOID BETA-PROTEIN PRECURSOR [J].
CAI, XD ;
GOLDE, TE ;
YOUNKIN, SG .
SCIENCE, 1993, 259 (5094) :514-516
[5]   APOPTOSIS AND DISEASE [J].
CARSON, DA ;
RIBEIRO, JM .
LANCET, 1993, 341 (8855) :1251-1254
[6]   EFFICIENCY OF UTILIZATION OF THE SIMIAN VIRUS-40 LATE POLYADENYLATION SITE - EFFECTS OF UPSTREAM SEQUENCES [J].
CARSWELL, S ;
ALWINE, JC .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (10) :4248-4258
[7]   MUTATION OF THE BETA-AMYLOID PRECURSOR PROTEIN IN FAMILIAL ALZHEIMERS-DISEASE INCREASES BETA-PROTEIN PRODUCTION [J].
CITRON, M ;
OLTERSDORF, T ;
HAASS, C ;
MCCONLOGUE, L ;
HUNG, AY ;
SEUBERT, P ;
VIGOPELFREY, C ;
LIEBERBURG, I ;
SELKOE, DJ .
NATURE, 1992, 360 (6405) :672-674
[8]  
COHEN JJ, 1993, IMMUNOL TODAY, V14, P126, DOI 10.1016/0167-5699(93)90214-6
[9]   BETA-AMYLOID NEUROTOXICITY - A DISCUSSION OF INVITRO FINDINGS [J].
COTMAN, CW ;
PIKE, CJ ;
COPANI, A .
NEUROBIOLOGY OF AGING, 1992, 13 (05) :587-590
[10]   GENERAL AND DRAMATIC GLIAL REACTION IN ALZHEIMER BRAINS [J].
DELACOURTE, A .
NEUROLOGY, 1990, 40 (01) :33-37