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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...

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Detalles Bibliográficos
Autores principales: Ryan, Sean K., Jordan-Sciutto, Kelly L., Anderson, Stewart A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
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).
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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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