胶质增生
疾病
神经炎症
神经科学
单纯疱疹病毒
陶氏病
人脑
炎症
小胶质细胞
淀粉样蛋白(真菌学)
生物
老年斑
医学
阿尔茨海默病
病理
免疫学
神经退行性变
病毒
作者
Dana M. Cairns,Nicolas Rouleau,Rachael N. Parker,Katherine G. Walsh,Lee Gehrke,David L. Kaplan
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2020-05-08
卷期号:6 (19)
被引量:165
标识
DOI:10.1126/sciadv.aay8828
摘要
Alzheimer's disease (AD) is a neurodegenerative disorder that causes cognitive decline, memory loss, and inability to perform everyday functions. Hallmark features of AD-including generation of amyloid plaques, neurofibrillary tangles, gliosis, and inflammation in the brain-are well defined; however, the cause of the disease remains elusive. Growing evidence implicates pathogens in AD development, with herpes simplex virus type I (HSV-1) gaining increasing attention as a potential causative agent. Here, we describe a multidisciplinary approach to produce physiologically relevant human tissues to study AD using human-induced neural stem cells (hiNSCs) and HSV-1 infection in a 3D bioengineered brain model. We report a herpes-induced tissue model of AD that mimics human disease with multicellular amyloid plaque-like formations, gliosis, neuroinflammation, and decreased functionality, completely in the absence of any exogenous mediators of AD. This model will allow for future studies to identify potential downstream drug targets for treating this devastating disease.
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