Mohd Idris, Izyan and Nordin, Fazlina and Muhamad, Nur Jannaim and Jalil, Julaina Abdul and Diana, Fatimah and Ordin, Aminn and Mohamed, Rosnani and Matripen, Adiratna and Tye, Gee Jun and Zaman, Wan Safwani Wankamarul and Yazid, Muhammad Dain and Hweing, Min (2023) The establishment of in vitro human induced pluripotent stem cell-derived. Sains Malaysiana, 52 (3). pp. 863-876. ISSN 0126-6039, DOI https://doi.org/10.17576/jsm-2023-5203-14.
Full text not available from this repository.Abstract
Induced pluripotent stem cells (iPSCs) have been generated using different reprogramming strategies. Lentiviruses remain a strategic method for cell reprogramming as it is highly efficient in gene transfer. The latest fourth-generation lentiviral packaging systems claimed to be efficient and safe. However, modifications made to enhance safety of lentiviral vectors have been shown to affect vector performance. In this study, we established that the fourthgeneration lentiviral packaging system can produce high-titre lentiviruses with high-transduction efficiencies. Subsequently, the robustness and reproducibility of generating iPSCs from adult human dermal fibroblasts were tested using these lentiviruses. The use of fourth-generation lentiviruses consistently generates iPSCs with similar efficiency and quality in different primary cell lines. This study demonstrated that the human-derived iPSCs can be maintained using mitomycin-C inactivated feeder cells. The iPSCs clones highly expressed key pluripotency markers and can spontaneously differentiate into cells from the three embryonic germ layers. The iPSCs generated were able to differentiate into neural stem cell lineages, producing cells expressing Nestin and Sox2 as well as able to further differentiate into neurons with more than 70% efficiency. The data demonstrated that the use of the fourth-generation lentiviral packaging to produce lentiviruses for iPSCs generation is robust and reproducible as it can generate iPSCs from different adult dermal fibroblasts with the potential to differentiate into neural stem cells and neurons. The use of safer lentiviral packaging systems combined with established vector plasmids will help to expedite the generation of iPSCs for clinical applications.
| Item Type: | Article |
|---|---|
| Funders: | None |
| Uncontrolled Keywords: | Induced pluripotent stem cells; Lentivirus; Neural stem cells; Neurons; Reprogramming |
| Subjects: | R Medicine > R Medicine (General) > Medical technology T Technology > T Technology (General) |
| Divisions: | Faculty of Engineering > Biomedical Engineering Department |
| Depositing User: | Ms Zaharah Ramly |
| Date Deposited: | 10 Nov 2024 05:16 |
| Last Modified: | 10 Nov 2024 05:16 |
| URI: | http://eprints.um.edu.my/id/eprint/38502 |
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