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阿尔茨海默病中β淀粉样蛋白的生物学特性

Biology of A beta amyloid in Alzheimer's disease.

作者信息

Wisniewski T, Ghiso J, Frangione B

机构信息

Department of Neurology, New York University Medical Center, New York 10016, USA.

出版信息

Neurobiol Dis. 1997;4(5):313-28. doi: 10.1006/nbdi.1997.0147.

Abstract

The genetic associations with the pathological features of AD are diverse: A rapidly growing number of mutations in presenilin 1 and 2 on chromosomes 14 and 1, respectively, are found in many early-onset FAD patients (Lendon et al., 1997). In addition, beta PP mutations are found in a small percentage of early-onset FAD kindreds. The apoE4 allele on chromosome 19 is associated with the presence of the most common form of AD, sporadic AD (Wisniewski & Frangione, 1992; Namba et al., 1991). However, it is clear that other proteins are also involved in the pathogenesis of AD, since some early-onset FAD kindreds do not have linkage to PS1, PS2, apoE, or beta PP, while at least 50% of late-onset AD is unrelated to apoE. Other proteins which have been implicated in the formation of senile plaques, but so far are not known to have any genetic linkage to AD, include proteoglycans (Snow et al., 1987), apoA1 (Wisniewski et al., 1995a), alpha 1-antichymotrypsin (Abraham et al., 1988), HB-GAM (Wisniewski et al., 1996a), complement components (McGeer & Rogers, 1992), acetylcholinesterase (Friede, 1965), and NAC (Ueda et al., 1993). Which of these proteins will be the most important for the etiology of the most common form of AD, late-onset sporadic AD, remains an open question. Three of the genes which are now known to be linked to AD, including PS1, beta PP, and apoE, have been established immunohistochemically and biochemically to be components of senile plaques (see Fig. 1). This raises at least two possibilities: either each of these proteins is part of one pathway with A beta-related amyloid formation as a final causative pathogenic event or amyloid deposition in AD is a reactive process related to dysfunction of a number of different CNS proteins. Whether or not amyloid formation is directly causative in the pathogenesis of AD, current data suggest that new therapeutic approaches which may inhibit the aggregation and/or the conformational change of sA beta to A beta fibrils (Soto et al., 1996) have the greatest likelihood to make a significant impact on controlling amyloid accumulation in AD.

摘要

与阿尔茨海默病(AD)病理特征相关的基因多种多样:分别在14号和1号染色体上的早老素1和早老素2中发现,越来越多的突变存在于许多早发性家族性阿尔茨海默病(FAD)患者中(伦登等人,1997年)。此外,在一小部分早发性FAD家族中发现了β淀粉样前体蛋白(beta PP)突变。19号染色体上的载脂蛋白E4(apoE4)等位基因与最常见形式的AD即散发性AD的存在有关(维斯涅夫斯基和弗兰焦内,1992年;南波等人,1991年)。然而,很明显其他蛋白质也参与了AD的发病机制,因为一些早发性FAD家族与早老素1(PS1)、早老素2(PS2)、载脂蛋白E(apoE)或beta PP没有连锁关系,而至少50%的晚发性AD与apoE无关。其他一些与老年斑形成有关但目前尚不清楚与AD有任何基因连锁关系的蛋白质包括蛋白聚糖(斯诺等人,1987年)、载脂蛋白A1(维斯涅夫斯基等人,1995a)、α1抗糜蛋白酶(亚伯拉罕等人,1988年)、人绒毛膜促性腺激素(HB-GAM)(维斯涅夫斯基等人,1996a)、补体成分(麦吉尔和罗杰斯,1992年)、乙酰胆碱酯酶(弗里德,1965年)和NAC(上田等人,1993年)。这些蛋白质中哪一种对最常见形式的AD即晚发性散发性AD的病因最为重要,仍然是一个悬而未决的问题。目前已知与AD相关的三个基因,包括PS1、beta PP和apoE,已通过免疫组织化学和生物化学方法确定为老年斑的成分(见图1)。这至少提出了两种可能性:要么这些蛋白质中的每一种都是与β淀粉样蛋白(Aβ)相关的淀粉样蛋白形成这一最终致病病理事件的一个途径的一部分,要么AD中的淀粉样蛋白沉积是一个与多种不同中枢神经系统蛋白质功能障碍相关的反应过程。无论淀粉样蛋白形成在AD发病机制中是否直接起因果作用,目前的数据表明,可能抑制可溶性Aβ(sAβ)聚集和/或向Aβ纤维的构象变化的新治疗方法(索托等人,1996年)最有可能对控制AD中的淀粉样蛋白积累产生重大影响。

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