Departamento Biologia Celular, Genetica y Fisiologia, Instituto de Investigacion Biomedica de Malaga-IBIMA, Facultad de Ciencias, Universidad de Malaga, 29071 Malaga, Spain.
Centro de Investigacion Biomedica en Red Sobre Enfermedades Neurodegenerativas (CIBERNED), 28031 Madrid, Spain.
Int J Mol Sci. 2022 May 12;23(10):5404. doi: 10.3390/ijms23105404.
Alzheimer's disease (AD) constitutes the most prominent form of dementia among elderly individuals worldwide. Disease modeling using murine transgenic mice was first initiated thanks to the discovery of heritable mutations in amyloid precursor protein (APP) and presenilins (PS) genes. However, due to the repeated failure of translational applications from animal models to human patients, along with the recent advances in genetic susceptibility and our current understanding on disease biology, these models have evolved over time in an attempt to better reproduce the complexity of this devastating disease and improve their applicability. In this review, we provide a comprehensive overview about the major pathological elements of human AD (plaques, tauopathy, synaptic damage, neuronal death, neuroinflammation and glial dysfunction), discussing the knowledge that available mouse models have provided about the mechanisms underlying human disease. Moreover, we highlight the pros and cons of current models, and the revolution offered by the concomitant use of transgenic mice and omics technologies that may lead to a more rapid improvement of the present modeling battery.
阿尔茨海默病(AD)构成了全球老年人中最突出的痴呆形式。由于在淀粉样前体蛋白(APP)和早老素(PS)基因中发现了遗传性突变,使用转基因小鼠的疾病模型首先得以建立。然而,由于动物模型向人类患者的转化应用一再失败,以及遗传易感性的最新进展和我们目前对疾病生物学的理解,这些模型随着时间的推移不断发展,试图更好地复制这种破坏性疾病的复杂性并提高其适用性。在这篇综述中,我们全面概述了人类 AD 的主要病理元素(斑块、tau 病、突触损伤、神经元死亡、神经炎症和神经胶质功能障碍),讨论了现有小鼠模型为人类疾病机制提供的知识。此外,我们还强调了当前模型的优缺点,以及转基因小鼠和组学技术的共同使用带来的变革,这可能会加速现有模型库的改进。