Inestrosa N C, Soto C
Department of Cellular and Molecular Biology, Faculty of Biological Sciences, P. Catholic University of Chile, Santiago.
Biol Res. 1992;25(2):63-72.
Alzheimer's disease is a progressive neurodegenerative disorder that affects a significant percentage of elderly individuals. Degenerative nerve cells express atypical proteins, and amyloid is deposited. The hallmark event of Alzheimer's disease is the deposition of amyloid as insoluble fibrous masses in extracellular neuritic plaques and around the walls of cerebral blood vessels. This review will focus on the advances on the knowledge of Alzheimer's amyloid, because it is becoming increasingly clear that the deposition of amyloid on neuritic plaques in the brain represents the earliest and most characteristic pathological feature of Alzheimer's disease. The main component of amyloid is a 4.2-4.5 KDa hydrophobic peptide, named amyloid beta-peptide, that is codified in chromosome 21 as part of a much larger precursor protein. The study of the mechanism by which the amyloid beta-peptide arises from the amyloid precursor protein is very important in order to understand the biological basis of amyloid deposition and its role in Alzheimer's disease.
阿尔茨海默病是一种进行性神经退行性疾病,影响着相当比例的老年人。退化的神经细胞表达非典型蛋白质,并且淀粉样蛋白会沉积。阿尔茨海默病的标志性事件是淀粉样蛋白以不溶性纤维团块的形式沉积在细胞外神经炎性斑块和脑血管壁周围。这篇综述将聚焦于阿尔茨海默病淀粉样蛋白知识的进展,因为越来越清楚的是,大脑中神经炎性斑块上淀粉样蛋白的沉积代表了阿尔茨海默病最早且最具特征性的病理特征。淀粉样蛋白的主要成分是一种4.2 - 4.5千道尔顿的疏水肽,名为β淀粉样肽,它在21号染色体上作为一个大得多的前体蛋白的一部分被编码。为了理解淀粉样蛋白沉积的生物学基础及其在阿尔茨海默病中的作用,研究β淀粉样肽从淀粉样前体蛋白产生的机制非常重要。