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Generation of iPSC-based human-mouse microglial brain chimeras to study senescence of human microglia

Here, we provide a step-by-step protocol for generating human induced pluripotent stem cell (hiPSC)-based microglial mouse brain chimeras. In addition, we detail steps for intracerebral injection of pathological tau and magnetic cell isolation of human microglia from chimeric mouse brains for single...

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Detalles Bibliográficos
Autores principales: Jin, Mengmeng, Ma, Ziyuan, Jiang, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667309/
https://www.ncbi.nlm.nih.gov/pubmed/36595906
http://dx.doi.org/10.1016/j.xpro.2022.101847
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author Jin, Mengmeng
Ma, Ziyuan
Jiang, Peng
author_facet Jin, Mengmeng
Ma, Ziyuan
Jiang, Peng
author_sort Jin, Mengmeng
collection PubMed
description Here, we provide a step-by-step protocol for generating human induced pluripotent stem cell (hiPSC)-based microglial mouse brain chimeras. In addition, we detail steps for intracerebral injection of pathological tau and magnetic cell isolation of human microglia from chimeric mouse brains for single-cell RNA sequencing. Human microglia developed in chimeric mouse brains recapitulate the pathophysiology of microglia in human brain tissue, offering unprecedented opportunities to study human microglial senescence in vivo. For complete details on the use and execution of this protocol, please refer to (Jin et al., 2022b).
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spelling pubmed-96673092022-11-17 Generation of iPSC-based human-mouse microglial brain chimeras to study senescence of human microglia Jin, Mengmeng Ma, Ziyuan Jiang, Peng STAR Protoc Protocol Here, we provide a step-by-step protocol for generating human induced pluripotent stem cell (hiPSC)-based microglial mouse brain chimeras. In addition, we detail steps for intracerebral injection of pathological tau and magnetic cell isolation of human microglia from chimeric mouse brains for single-cell RNA sequencing. Human microglia developed in chimeric mouse brains recapitulate the pathophysiology of microglia in human brain tissue, offering unprecedented opportunities to study human microglial senescence in vivo. For complete details on the use and execution of this protocol, please refer to (Jin et al., 2022b). Elsevier 2022-11-12 /pmc/articles/PMC9667309/ /pubmed/36595906 http://dx.doi.org/10.1016/j.xpro.2022.101847 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Jin, Mengmeng
Ma, Ziyuan
Jiang, Peng
Generation of iPSC-based human-mouse microglial brain chimeras to study senescence of human microglia
title Generation of iPSC-based human-mouse microglial brain chimeras to study senescence of human microglia
title_full Generation of iPSC-based human-mouse microglial brain chimeras to study senescence of human microglia
title_fullStr Generation of iPSC-based human-mouse microglial brain chimeras to study senescence of human microglia
title_full_unstemmed Generation of iPSC-based human-mouse microglial brain chimeras to study senescence of human microglia
title_short Generation of iPSC-based human-mouse microglial brain chimeras to study senescence of human microglia
title_sort generation of ipsc-based human-mouse microglial brain chimeras to study senescence of human microglia
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667309/
https://www.ncbi.nlm.nih.gov/pubmed/36595906
http://dx.doi.org/10.1016/j.xpro.2022.101847
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