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阿尔茨海默病:遗传学研究与转基因模型

Alzheimer's disease: genetic studies and transgenic models.

作者信息

Price D L, Tanzi R E, Borchelt D R, Sisodia S S

机构信息

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2196, USA.

出版信息

Annu Rev Genet. 1998;32:461-93. doi: 10.1146/annurev.genet.32.1.461.

Abstract

Recent advances in a variety of areas of research, particularly in genetics and in transgenic (Tg)/gene targeting approaches, have had a substantial impact on our understanding of Alzheimer's disease (AD) and related disorders. After briefly reviewing the progress that has been made in diagnostic assessments of patients with senile dementia and in investigations of the neuropathology of AD, we discuss some of the genes/proteins that are causative or risk factors for this disease, including those encoding amyloid precursor protein, presenilin 1 and 2, and apolipoprotein E. In addition, we comment on several potential new candidate loci/genes. Subsequently, we review selected recent reports of analyses of a variety of lines of Tg mice that show several neuropathological features of AD, including A beta-amyloid deposits and dystrophic neurites. Finally, we discuss the several important issues in future investigations of Tg mice, with particular emphasis on the influences of genetic strains on phenotype, especially behavior, and strategies for making new models of neurodegenerative disorders. We believe that investigations of these Tg models will (a) enhance understanding of the relationships between impaired performance on memory tasks and the pathological/biochemical abnormalities in brain, (b) help to clarify pathogenic mechanisms in vivo, (c) lead to identification of new therapeutic targets, and (d) allow testing of new treatment strategies first in mice and then, if successful, in humans with AD.

摘要

多个研究领域的最新进展,尤其是遗传学以及转基因(Tg)/基因靶向方法方面的进展,对我们理解阿尔茨海默病(AD)及相关疾病产生了重大影响。在简要回顾老年痴呆患者诊断评估以及AD神经病理学研究取得的进展之后,我们讨论了一些导致该疾病的基因/蛋白质或风险因素,包括那些编码淀粉样前体蛋白、早老素1和2以及载脂蛋白E的基因/蛋白质。此外,我们对几个潜在的新候选基因座/基因进行了评论。随后,我们回顾了近期有关多种Tg小鼠品系分析的部分报告,这些小鼠表现出AD的几种神经病理学特征,包括β-淀粉样蛋白沉积和营养不良性神经突。最后,我们讨论了Tg小鼠未来研究中的几个重要问题,特别强调了遗传品系对表型尤其是行为的影响,以及构建神经退行性疾病新模型的策略。我们相信对这些Tg模型的研究将(a)增进对记忆任务表现受损与大脑病理/生化异常之间关系的理解,(b)有助于阐明体内致病机制,(c)导致新治疗靶点的识别,以及(d)首先在小鼠中测试新的治疗策略,若成功则随后在AD患者中进行测试。

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