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Generation and validation of APOE knockout human iPSC-derived cerebral organoids
Apolipoprotein E (apoE) is a major lipid carrier in the brain and closely associated with the pathogenesis of Alzheimer's disease (AD). Here, we describe a protocol for efficient knockout of APOE in human induced pluripotent stem cells (iPSCs) using the CRISPR-Cas9 system. We obtain homozygous...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190508/ https://www.ncbi.nlm.nih.gov/pubmed/34151296 http://dx.doi.org/10.1016/j.xpro.2021.100571 |
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author | Martens, Yuka A. Xu, Siming Tait, Richard Li, Gary Zhao, Xinping C. Lu, Wenyan Liu, Chia-Chen Kanekiyo, Takahisa Bu, Guojun Zhao, Jing |
author_facet | Martens, Yuka A. Xu, Siming Tait, Richard Li, Gary Zhao, Xinping C. Lu, Wenyan Liu, Chia-Chen Kanekiyo, Takahisa Bu, Guojun Zhao, Jing |
author_sort | Martens, Yuka A. |
collection | PubMed |
description | Apolipoprotein E (apoE) is a major lipid carrier in the brain and closely associated with the pathogenesis of Alzheimer's disease (AD). Here, we describe a protocol for efficient knockout of APOE in human induced pluripotent stem cells (iPSCs) using the CRISPR-Cas9 system. We obtain homozygous APOE knockout (APOE(-/-)) iPSCs and further validate the deficiency of apoE in iPSC-derived cerebral organoids. APOE(-/-) cerebral organoids can serve as a useful tool to study apoE functions and apoE-related pathogenic mechanisms in AD. For complete details on the use and execution of this protocol, please refer to Zhao et al. (2020). |
format | Online Article Text |
id | pubmed-8190508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81905082021-06-17 Generation and validation of APOE knockout human iPSC-derived cerebral organoids Martens, Yuka A. Xu, Siming Tait, Richard Li, Gary Zhao, Xinping C. Lu, Wenyan Liu, Chia-Chen Kanekiyo, Takahisa Bu, Guojun Zhao, Jing STAR Protoc Protocol Apolipoprotein E (apoE) is a major lipid carrier in the brain and closely associated with the pathogenesis of Alzheimer's disease (AD). Here, we describe a protocol for efficient knockout of APOE in human induced pluripotent stem cells (iPSCs) using the CRISPR-Cas9 system. We obtain homozygous APOE knockout (APOE(-/-)) iPSCs and further validate the deficiency of apoE in iPSC-derived cerebral organoids. APOE(-/-) cerebral organoids can serve as a useful tool to study apoE functions and apoE-related pathogenic mechanisms in AD. For complete details on the use and execution of this protocol, please refer to Zhao et al. (2020). Elsevier 2021-06-05 /pmc/articles/PMC8190508/ /pubmed/34151296 http://dx.doi.org/10.1016/j.xpro.2021.100571 Text en © 2021 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 Martens, Yuka A. Xu, Siming Tait, Richard Li, Gary Zhao, Xinping C. Lu, Wenyan Liu, Chia-Chen Kanekiyo, Takahisa Bu, Guojun Zhao, Jing Generation and validation of APOE knockout human iPSC-derived cerebral organoids |
title | Generation and validation of APOE knockout human iPSC-derived cerebral organoids |
title_full | Generation and validation of APOE knockout human iPSC-derived cerebral organoids |
title_fullStr | Generation and validation of APOE knockout human iPSC-derived cerebral organoids |
title_full_unstemmed | Generation and validation of APOE knockout human iPSC-derived cerebral organoids |
title_short | Generation and validation of APOE knockout human iPSC-derived cerebral organoids |
title_sort | generation and validation of apoe knockout human ipsc-derived cerebral organoids |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190508/ https://www.ncbi.nlm.nih.gov/pubmed/34151296 http://dx.doi.org/10.1016/j.xpro.2021.100571 |
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