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

被引:167
作者
Cairns, Dana M. [1 ,2 ]
Rouleau, Nicolas [1 ,2 ]
Parker, Rachael N. [1 ]
Walsh, Katherine G. [3 ]
Gehrke, Lee [4 ]
Kaplan, David L. [1 ,2 ]
机构
[1] Tufts Univ, Dept Biomed Engn, Medford, MA 02155 USA
[2] Tufts Univ, Allen Discovery Ctr, Medford, MA 02155 USA
[3] Tufts Univ, Dept Biol, Medford, MA 02155 USA
[4] MIT, Inst Med Engn & Sci, Cambridge, MA 02142 USA
关键词
SIMPLEX-VIRUS TYPE-1; AMYLOID-BETA PEPTIDES; PLAQUE-FORMATION; INFECTION; PHOSPHORYLATION; AMYLOIDOGENESIS; ACCUMULATION; EXPRESSION; MECHANISM; OLIGOMERS;
D O I
10.1126/sciadv.aay8828
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
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页数:13
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