BETA-AMYLOID FROM ALZHEIMER-DISEASE BRAINS INHIBITS SPROUTING AND SURVIVAL OF SYMPATHETIC NEURONS

被引:111
作者
ROHER, AE
BALL, MJ
BHAVE, SV
WAKADE, AR
机构
[1] WAYNE STATE UNIV,SCH MED,DEPT PHARMACOL,DETROIT,MI 48201
[2] OREGON HLTH SCI UNIV,DIV NEUROPATHOL,PORTLAND,OR 97201
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0006-291X(91)91455-L
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
The significance of the amyloid plaque core proteins (APCP) in Alzheimer's disease (AD) and its consequences for neuronal survival have been controversial. To address this problem we purified the APCP and βA, obtained from brains with AD, and assessed their biological effects in tissue culture. APCP and βA caused severe toxicity to chick and rat sympathetic and sensory neurons whose survival is dependent upon NGF. This toxicity was dose dependent and reversible at low doses. APCP and βA prevented sprouting of neurites in freshly plated neurons. In established cultures addition of these molecules caused vacuolation and fragmentation of neurites and disintegration of neuronal soma. We suggest that the deposition of APCP in AD may be partly responsible for the destruction of the neuritic arbor, thereby contributing to the formation of the neuritic plaque and to neuronal death. © 1991.
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页码:572 / 579
页数:8
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