Cargando…

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

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Cairns, Dana M., Rouleau, Nicolas, Parker, Rachael N., Walsh, Katherine G., Gehrke, Lee, Kaplan, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202879/
https://www.ncbi.nlm.nih.gov/pubmed/32494701
http://dx.doi.org/10.1126/sciadv.aay8828
_version_ 1783529781284831232
author Cairns, Dana M.
Rouleau, Nicolas
Parker, Rachael N.
Walsh, Katherine G.
Gehrke, Lee
Kaplan, David L.
author_facet Cairns, Dana M.
Rouleau, Nicolas
Parker, Rachael N.
Walsh, Katherine G.
Gehrke, Lee
Kaplan, David L.
author_sort Cairns, Dana M.
collection PubMed
description 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.
format Online
Article
Text
id pubmed-7202879
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-72028792020-06-02 A 3D human brain–like tissue model of herpes-induced Alzheimer’s disease Cairns, Dana M. Rouleau, Nicolas Parker, Rachael N. Walsh, Katherine G. Gehrke, Lee Kaplan, David L. Sci Adv Research Articles 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. American Association for the Advancement of Science 2020-05-06 /pmc/articles/PMC7202879/ /pubmed/32494701 http://dx.doi.org/10.1126/sciadv.aay8828 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Cairns, Dana M.
Rouleau, Nicolas
Parker, Rachael N.
Walsh, Katherine G.
Gehrke, Lee
Kaplan, David L.
A 3D human brain–like tissue model of herpes-induced Alzheimer’s disease
title A 3D human brain–like tissue model of herpes-induced Alzheimer’s disease
title_full A 3D human brain–like tissue model of herpes-induced Alzheimer’s disease
title_fullStr A 3D human brain–like tissue model of herpes-induced Alzheimer’s disease
title_full_unstemmed A 3D human brain–like tissue model of herpes-induced Alzheimer’s disease
title_short A 3D human brain–like tissue model of herpes-induced Alzheimer’s disease
title_sort 3d human brain–like tissue model of herpes-induced alzheimer’s disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202879/
https://www.ncbi.nlm.nih.gov/pubmed/32494701
http://dx.doi.org/10.1126/sciadv.aay8828
work_keys_str_mv AT cairnsdanam a3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT rouleaunicolas a3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT parkerrachaeln a3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT walshkatherineg a3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT gehrkelee a3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT kaplandavidl a3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT cairnsdanam 3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT rouleaunicolas 3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT parkerrachaeln 3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT walshkatherineg 3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT gehrkelee 3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease
AT kaplandavidl 3dhumanbrainliketissuemodelofherpesinducedalzheimersdisease