A novel Polish presenilin-1 mutation (P117L) is associated with familial Alzheimer's disease and leads to death as early as the age of 28 years

被引:92
作者
Wisniewski, T
Dowjat, WK
Buxbaum, JD
Khorkova, O
Efthimiopoulos, S
Kulczycki, J
Lojkowska, W
Wegiel, J
Wisniewski, HM
Frangione, B
机构
[1] NYU Med Ctr, Dept Neurol, New York, NY 10016 USA
[2] NYU Med Ctr, Dept Pathol, New York, NY 10016 USA
[3] Mt Sinai Sch Med, Dept Psychiat, New York, NY USA
[4] Hoechst Marion Roussel, Somerville, NJ USA
[5] Inst Psychiat & Neurol, Warsaw, Poland
[6] New York State Inst Basic Res Dev Disabil, Staten Isl, NY 10314 USA
关键词
Alzheimer's disease; amyloid beta; mutation; presenilin; transfection;
D O I
10.1097/00001756-199801260-00008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE majority of early-onset familial Alzheimer's disease (FAD) is associated with mutations in the presenilin-1 (PS1) gene. We describe a novel Polish PS1 mutation of Pro117Leu, associated with the earliest average age of onset and death so far reported in a PS-linked, FAD kindred. Human kidney 293 and mouse neuroblastoma N2a cells were stably transfected with wild-type and PS1 P117L. There was a significant increase in the amyloid beta 42/40 ratio in the N2a P117L PS1 transfected cells compared with N2a transfected with wild-type PS1. What role PS has in the pathogenesis of AD remains to be determined, however, the severity of the clinical picture associated with this PS1 mutation stresses the importance of presenilin.
引用
收藏
页码:217 / 221
页数:5
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