A 3D human brain-like tissue model of herpes-induced Alzheimer's disease

Copyright © 2020 The Authors, 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...

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Main Authors: Cairns, Dana M (Author), Rouleau, Nicolas (Author), Parker, Rachael N (Author), Walsh, Katherine G (Author), Gehrke, Lee (Author), Kaplan, David L (Author)
Format: Article
Language:English
Published: American Association for the Advancement of Science (AAAS), 2021-12-08T19:22:24Z.
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Online Access:Get fulltext
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042 |a dc 
100 1 0 |a Cairns, Dana M  |e author 
700 1 0 |a Rouleau, Nicolas  |e author 
700 1 0 |a Parker, Rachael N  |e author 
700 1 0 |a Walsh, Katherine G  |e author 
700 1 0 |a Gehrke, Lee  |e author 
700 1 0 |a Kaplan, David L  |e author 
245 0 0 |a A 3D human brain-like tissue model of herpes-induced Alzheimer's disease 
260 |b American Association for the Advancement of Science (AAAS),   |c 2021-12-08T19:22:24Z. 
856 |z Get fulltext  |u https://hdl.handle.net/1721.1/138397 
520 |a Copyright © 2020 The Authors, 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. 
546 |a en 
655 7 |a Article 
773 |t 10.1126/SCIADV.AAY8828 
773 |t Science Advances