McGowan Eileen, Eriksen Jason, Hutton Michael
Department of Neuroscience, Mayo Clinic College of Medicine, 4500 San Pablo Road, Jacksonville, FL 32224, USA.
Trends Genet. 2006 May;22(5):281-9. doi: 10.1016/j.tig.2006.03.007. Epub 2006 Mar 29.
It has been over a decade since the first Alzheimer's disease (AD) transgenic mouse models were reported. These models have enabled dramatic advances in our understanding of the pathogenic mechanism in AD and of potential therapeutic approaches to tackling the inexorable clinical progression of the disease. In this article, we discuss the current status of AD mouse models and focus on recent work that has examined the development of the neuropathological lesions observed in AD (plaques and tangles). The relationship between these lesions, neurodegeneration and development of the clinical syndrome will be explored.
自首个阿尔茨海默病(AD)转基因小鼠模型被报道以来,已经过去了十多年。这些模型使我们在理解AD的致病机制以及应对该疾病无情临床进展的潜在治疗方法方面取得了巨大进展。在本文中,我们讨论了AD小鼠模型的现状,并重点关注了最近关于研究AD中观察到的神经病理损伤(斑块和缠结)发展情况的工作。我们将探讨这些损伤、神经退行性变与临床综合征发展之间的关系。