Hendriks L, Cras P, Martin J J, Broeckhoven C V
Born-Bunge Foundation, University of Antwerp, Department of Biochemistry, Belgium.
Ciba Found Symp. 1996;199:170-80. doi: 10.1002/9780470514924.ch11.
One of the major pathological hallmarks of Alzheimer's disease is the deposition in the brain parenchyma and cerebral blood vessel walls of amyloid beta-protein, a 4kDa proteolytic product of the longer beta-amyloid precursor protein (APP). Six different single base mutations in the APP gene have been reported causing early-onset Alzheimer's disease (age at onset < or = 65 years) or related amyloidosis in a small number of families. Cell transfection experiments using wild-type and mutant APP cDNA indicated that APP mutations result in the production of more or longer, aggregation prone, A beta peptides.
阿尔茨海默病的主要病理特征之一是淀粉样β蛋白在脑实质和脑血管壁中的沉积,淀粉样β蛋白是较长的β淀粉样前体蛋白(APP)的一种4kDa蛋白水解产物。据报道,APP基因中有六种不同的单碱基突变可导致早发性阿尔茨海默病(发病年龄≤65岁)或在少数家族中引发相关淀粉样变性。使用野生型和突变型APP cDNA进行的细胞转染实验表明,APP突变会导致产生更多或更长的、易于聚集的Aβ肽。