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Protocol for Tri-culture of hiPSC-Derived Neurons, Astrocytes, and Microglia
This protocol establishes a tri-culture of hiPSC-derived neurons, astrocytes, and microglia for the study of cellular interactions during homeostasis, injury, and disease. This system allows for mechanistic studies that can identify the roles of individual cell types in disease and injury response i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757552/ https://www.ncbi.nlm.nih.gov/pubmed/33377084 http://dx.doi.org/10.1016/j.xpro.2020.100190 |
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author | Ryan, Sean K. Jordan-Sciutto, Kelly L. Anderson, Stewart A. |
author_facet | Ryan, Sean K. Jordan-Sciutto, Kelly L. Anderson, Stewart A. |
author_sort | Ryan, Sean K. |
collection | PubMed |
description | This protocol establishes a tri-culture of hiPSC-derived neurons, astrocytes, and microglia for the study of cellular interactions during homeostasis, injury, and disease. This system allows for mechanistic studies that can identify the roles of individual cell types in disease and injury response in a physiologically relevant, all-human system. This protocol utilizes and modifies prior differentiations. Limitations include the prolonged maturation of human astrocytes and neurons and scalability. For complete details on the use and execution of this protocol, please refer to Ryan et al. (2020). |
format | Online Article Text |
id | pubmed-7757552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-77575522020-12-28 Protocol for Tri-culture of hiPSC-Derived Neurons, Astrocytes, and Microglia Ryan, Sean K. Jordan-Sciutto, Kelly L. Anderson, Stewart A. STAR Protoc Protocol This protocol establishes a tri-culture of hiPSC-derived neurons, astrocytes, and microglia for the study of cellular interactions during homeostasis, injury, and disease. This system allows for mechanistic studies that can identify the roles of individual cell types in disease and injury response in a physiologically relevant, all-human system. This protocol utilizes and modifies prior differentiations. Limitations include the prolonged maturation of human astrocytes and neurons and scalability. For complete details on the use and execution of this protocol, please refer to Ryan et al. (2020). Elsevier 2020-12-01 /pmc/articles/PMC7757552/ /pubmed/33377084 http://dx.doi.org/10.1016/j.xpro.2020.100190 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Protocol Ryan, Sean K. Jordan-Sciutto, Kelly L. Anderson, Stewart A. Protocol for Tri-culture of hiPSC-Derived Neurons, Astrocytes, and Microglia |
title | Protocol for Tri-culture of hiPSC-Derived Neurons, Astrocytes, and Microglia |
title_full | Protocol for Tri-culture of hiPSC-Derived Neurons, Astrocytes, and Microglia |
title_fullStr | Protocol for Tri-culture of hiPSC-Derived Neurons, Astrocytes, and Microglia |
title_full_unstemmed | Protocol for Tri-culture of hiPSC-Derived Neurons, Astrocytes, and Microglia |
title_short | Protocol for Tri-culture of hiPSC-Derived Neurons, Astrocytes, and Microglia |
title_sort | protocol for tri-culture of hipsc-derived neurons, astrocytes, and microglia |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757552/ https://www.ncbi.nlm.nih.gov/pubmed/33377084 http://dx.doi.org/10.1016/j.xpro.2020.100190 |
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