| Online-Ressource |
Verfasst von: | Hartley, Anna [VerfasserIn]  |
| Burger, Luisa [VerfasserIn]  |
| Wincek, Cornelia L. [VerfasserIn]  |
| Dons, Lieke [VerfasserIn]  |
| Li, Tracy [VerfasserIn]  |
| Grewenig, Annabel [VerfasserIn]  |
| Tasgin, Toros [VerfasserIn]  |
| Urban, Manuela Vanessa [VerfasserIn]  |
| Roig-Merino, Alicia [VerfasserIn]  |
| Ghazvini, Mehrnaz [VerfasserIn]  |
| Harbottle, Richard P. [VerfasserIn]  |
Titel: | A simple nonviral method to generate human induced pluripotent stem cells using SMAR DNA vectors |
Verf.angabe: | Anna Hartley, Luisa Burger, Cornelia L. Wincek, Lieke Dons, Tracy Li, Annabel Grewenig, Toros Taşgın, Manuela Urban, Alicia Roig-Merino, Mehrnaz Ghazvini and Richard P. Harbottle |
E-Jahr: | 2024 |
Jahr: | 30 April 2024 |
Umfang: | 17 S. |
Illustrationen: | Illustrationen |
Fussnoten: | Gesehen am 11.06.2025 |
Titel Quelle: | Enthalten in: Genes |
Ort Quelle: | Basel : MDPI, 2009 |
Jahr Quelle: | 2024 |
Band/Heft Quelle: | 15(2024), 5, Artikel-ID 575, Seite 1-17 |
ISSN Quelle: | 2073-4425 |
Abstract: | Induced pluripotent stem cells (iPSCs) are a powerful tool for biomedical research, but their production presents challenges and safety concerns. Yamanaka and Takahashi revolutionised the field by demonstrating that somatic cells could be reprogrammed into pluripotent cells by overexpressing four key factors for a sufficient time. iPSCs are typically generated using viruses or virus-based methods, which have drawbacks such as vector persistence, risk of insertional mutagenesis, and oncogenesis. The application of less harmful nonviral vectors is limited as conventional plasmids cannot deliver the levels or duration of the factors necessary from a single transfection. Hence, plasmids that are most often used for reprogramming employ the potentially oncogenic Epstein-Barr nuclear antigen 1 (EBNA-1) system to ensure adequate levels and persistence of expression. In this study, we explored the use of nonviral SMAR DNA vectors to reprogram human fibroblasts into iPSCs. We show for the first time that iPSCs can be generated using nonviral plasmids without the use of EBNA-1 and that these DNA vectors can provide sufficient expression to induce pluripotency. We describe an optimised reprogramming protocol using these vectors that can produce high-quality iPSCs with comparable pluripotency and cellular function to those generated with viruses or EBNA-1 vectors. |
DOI: | doi:10.3390/genes15050575 |
URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
kostenfrei: Volltext: https://doi.org/10.3390/genes15050575 |
| kostenfrei: Volltext: https://www.mdpi.com/2073-4425/15/5/575 |
| DOI: https://doi.org/10.3390/genes15050575 |
Datenträger: | Online-Ressource |
Sprache: | eng |
Sach-SW: | Cells, Cultured |
| Cellular Reprogramming |
| Epstein-Barr Virus Nuclear Antigens |
| Fibroblasts |
| Genetic Vectors |
| Humans |
| Induced Pluripotent Stem Cells |
| iPSC |
| nonviral |
| Plasmids |
| reprogramming |
| S/MAR |
| SMAR DNA vector |
| stem cells |
| Transfection |
K10plus-PPN: | 1927943345 |
Verknüpfungen: | → Zeitschrift |
¬A¬ simple nonviral method to generate human induced pluripotent stem cells using SMAR DNA vectors / Hartley, Anna [VerfasserIn]; 30 April 2024 (Online-Ressource)