Sara Cuevas Ocana
How can gene-editing of human pluripotent stem cells help cystic fibrosis?
Cuevas Ocana, Sara; Wong, Amy; Aushev, Magomet; Ye Yang, Jin; Perkins, Neil; Bear, Christine; Rossant, Janet; Gray, Michael
Authors
Amy Wong
Magomet Aushev
Jin Ye Yang
Neil Perkins
Christine Bear
Janet Rossant
Michael Gray
Abstract
Cystic fibrosis (CF) is a monogenic recessive disorder, affecting 70,000 people worldwide. CF is due to mutations in the CFTR gene, resulting in a defective protein that leads to symptoms in numerous organs, especially lungs. Despite recent advances, the lack of CF material contributes to the unmet need to find effective treatments for 55% of CF patients, and to restore the function of all affected tissues.
A potential strategy would be to use gene-editing technologies (TALENs or CRISPR/Cas9) to introduce into or correct specific mutations in pluripotent stem cells (hPSCs) that can be turned into any other cell type. But current protocols for gene-editing hPSCs are often complicated, lengthy (6-8 months) and costly, thus, being restricted to a few specialised labs.
This study describes an optimised protocol to correct the W1282X mutation in 3 CF hPSC lines derived from an adult and children with CF (iPSCs), by transfecting a CRISPR/Cas9 plasmid, a selection plasmid and a donor template. Corrected iPSCs were produced in 3-6 weeks. This protocol was previously used to generate the most common CF genotype, ∆F508/∆F508, from healthy hPSCs using TALENs.
This work demonstrated that optimising each step of the gene-editing process, including an efficient transfection of hPSCs, and rapid isolation and screening for corrected cells, can produce in vitro models for CF in less than one month with minimum costs. These cells generated from paediatric or adult CF patients can be used to generate mutation-customised tissue-specific cultures holding great promise to advance drug testing and personalised medicine for CF.
Citation
Cuevas Ocana, S., Wong, A., Aushev, M., Ye Yang, J., Perkins, N., Bear, C., Rossant, J., & Gray, M. How can gene-editing of human pluripotent stem cells help cystic fibrosis?. Presented at ERS International Congress 2019, Madrid, Spain
Presentation Conference Type | Conference Abstract |
---|---|
Conference Name | ERS International Congress 2019 |
Online Publication Date | Nov 21, 2019 |
Publication Date | 2019 |
Deposit Date | Aug 10, 2023 |
Journal | European Respiratory Journal |
Print ISSN | 0903-1936 |
Electronic ISSN | 1399-3003 |
Publisher | European Respiratory Society |
Peer Reviewed | Peer Reviewed |
Volume | 54 |
Issue | suppl 63 |
Article Number | OA2125 |
DOI | https://doi.org/10.1183/13993003.congress-2019.oa2125 |
Public URL | https://nottingham-repository.worktribe.com/output/23574680 |
Publisher URL | https://erj.ersjournals.com/content/54/suppl_63/OA2125 |
Additional Information | This is an ERS International Congress abstract |
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