Improving mouse models for the study of Alzheimer's disease.

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
Alaina M Reagan, Kristen D Onos, Sarah E Heuer, Michael Sasner, Gareth R Howell
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引用次数: 0

Abstract

Alzheimer's disease (AD) is a complex neurodegenerative disease whose risk is influenced by genetic and environmental factors. Although a number of pathological hallmarks have been extensively studied over the last several decades, a complete picture of disease initiation and progression remains unclear. We now understand that numerous cell types and systems are involved in AD pathogenesis, and that this cellular profile may present differently for each individual, making the creation of relevant mouse models challenging. However, with increasingly diverse data made available by genome-wide association studies, we can identify and examine new genes and pathways involved in genetic risk for AD, many of which involve vascular health and inflammation. When developing mouse models, it is critical to assess (1) an aging timeline that represents onset and progression in humans, (2) genetic variants and context, (3) environmental factors present in human populations that result in both neuropathological and functional changes-themes that we address in this chapter.

改进阿尔茨海默病研究的小鼠模型。
阿尔茨海默病(AD)是一种复杂的神经退行性疾病,其发病风险受遗传和环境因素的影响。尽管在过去的几十年里,许多病理特征已经被广泛研究,但疾病发生和发展的完整图景仍然不清楚。我们现在了解到,许多细胞类型和系统参与了AD的发病机制,并且每个个体的细胞特征可能不同,这使得相关小鼠模型的创建具有挑战性。然而,随着全基因组关联研究提供的数据越来越多样化,我们可以识别和检查与阿尔茨海默病遗传风险相关的新基因和途径,其中许多涉及血管健康和炎症。在开发小鼠模型时,至关重要的是评估(1)代表人类发病和进展的衰老时间表,(2)遗传变异和背景,(3)导致神经病理和功能变化的人群中存在的环境因素-我们在本章中讨论的主题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
91
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