Cargando…
Modelling Zika Virus Infection of the Developing Human Brain In Vitro Using Stem Cell Derived Cerebral Organoids
The recent emergence of Zika virus (ZIKV) in susceptible populations has led to an abrupt increase in microcephaly and other neurodevelopmental conditions in newborn infants. While mosquitos are the main route of viral transmission, it has also been shown to spread via sexual contact and vertical mo...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752258/ https://www.ncbi.nlm.nih.gov/pubmed/28994790 http://dx.doi.org/10.3791/56404 |
_version_ | 1783290096215130112 |
---|---|
author | Salick, Max R Wells, Michael F Eggan, Kevin Kaykas, Ajamete |
author_facet | Salick, Max R Wells, Michael F Eggan, Kevin Kaykas, Ajamete |
author_sort | Salick, Max R |
collection | PubMed |
description | The recent emergence of Zika virus (ZIKV) in susceptible populations has led to an abrupt increase in microcephaly and other neurodevelopmental conditions in newborn infants. While mosquitos are the main route of viral transmission, it has also been shown to spread via sexual contact and vertical mother-to-fetus transmission. In this latter case of transmission, due to the unique viral tropism of ZIKV, the virus is believed to predominantly target the neural progenitor cells (NPCs) of the developing brain. Here a method for modeling ZIKV infection, and the resulting microcephaly, that occur when human cerebral organoids are exposed to live ZIKV is described. The organoids display high levels of virus within their neural progenitor population, and exhibit severe cell death and microcephaly over time. This three-dimensional cerebral organoid model allows researchers to conduct species-matched experiments to observe and potentially intervene with ZIKV infection of the developing human brain. The model provides improved relevance over standard two-dimensional methods, and contains human-specific cellular architecture and protein expression that are not possible in animal models. |
format | Online Article Text |
id | pubmed-5752258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-57522582018-01-19 Modelling Zika Virus Infection of the Developing Human Brain In Vitro Using Stem Cell Derived Cerebral Organoids Salick, Max R Wells, Michael F Eggan, Kevin Kaykas, Ajamete J Vis Exp Neuroscience The recent emergence of Zika virus (ZIKV) in susceptible populations has led to an abrupt increase in microcephaly and other neurodevelopmental conditions in newborn infants. While mosquitos are the main route of viral transmission, it has also been shown to spread via sexual contact and vertical mother-to-fetus transmission. In this latter case of transmission, due to the unique viral tropism of ZIKV, the virus is believed to predominantly target the neural progenitor cells (NPCs) of the developing brain. Here a method for modeling ZIKV infection, and the resulting microcephaly, that occur when human cerebral organoids are exposed to live ZIKV is described. The organoids display high levels of virus within their neural progenitor population, and exhibit severe cell death and microcephaly over time. This three-dimensional cerebral organoid model allows researchers to conduct species-matched experiments to observe and potentially intervene with ZIKV infection of the developing human brain. The model provides improved relevance over standard two-dimensional methods, and contains human-specific cellular architecture and protein expression that are not possible in animal models. MyJove Corporation 2017-09-19 /pmc/articles/PMC5752258/ /pubmed/28994790 http://dx.doi.org/10.3791/56404 Text en Copyright © 2017, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Neuroscience Salick, Max R Wells, Michael F Eggan, Kevin Kaykas, Ajamete Modelling Zika Virus Infection of the Developing Human Brain In Vitro Using Stem Cell Derived Cerebral Organoids |
title | Modelling Zika Virus Infection of the Developing Human Brain In Vitro Using Stem Cell Derived Cerebral Organoids |
title_full | Modelling Zika Virus Infection of the Developing Human Brain In Vitro Using Stem Cell Derived Cerebral Organoids |
title_fullStr | Modelling Zika Virus Infection of the Developing Human Brain In Vitro Using Stem Cell Derived Cerebral Organoids |
title_full_unstemmed | Modelling Zika Virus Infection of the Developing Human Brain In Vitro Using Stem Cell Derived Cerebral Organoids |
title_short | Modelling Zika Virus Infection of the Developing Human Brain In Vitro Using Stem Cell Derived Cerebral Organoids |
title_sort | modelling zika virus infection of the developing human brain in vitro using stem cell derived cerebral organoids |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752258/ https://www.ncbi.nlm.nih.gov/pubmed/28994790 http://dx.doi.org/10.3791/56404 |
work_keys_str_mv | AT salickmaxr modellingzikavirusinfectionofthedevelopinghumanbraininvitrousingstemcellderivedcerebralorganoids AT wellsmichaelf modellingzikavirusinfectionofthedevelopinghumanbraininvitrousingstemcellderivedcerebralorganoids AT eggankevin modellingzikavirusinfectionofthedevelopinghumanbraininvitrousingstemcellderivedcerebralorganoids AT kaykasajamete modellingzikavirusinfectionofthedevelopinghumanbraininvitrousingstemcellderivedcerebralorganoids |