دورية أكاديمية
Targeted gene silencing in human embryonic stem cells using cell-penetrating peptide PepFect 14
| العنوان: | Targeted gene silencing in human embryonic stem cells using cell-penetrating peptide PepFect 14 |
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| المؤلفون: | Egle-Helene Ervin, Martin Pook, Indrek Teino, Valmar Kasuk, Annika Trei, Margus Pooga, Toivo Maimets |
| المصدر: | Stem Cell Research & Therapy, Vol 10, Iss 1, Pp 1-14 (2019) |
| بيانات النشر: | BMC, 2019. |
| سنة النشر: | 2019 |
| المجموعة: | LCC:Medicine (General) LCC:Biochemistry |
| مصطلحات موضوعية: | Human embryonic stem cells, siRNA transfection, Cell-penetrating peptide, PepFect 14, OCT4, B2M, Medicine (General), R5-920, Biochemistry, QD415-436 |
| الوصف: | Abstract Background Human embryonic stem (hES) cells serve as an invaluable tool for research and future medicine, but their transfection often leads to unwanted side effects as the method itself may induce differentiation. On the other hand, RNA interference (RNAi)-based targeted gene silencing is a quick, cost-effective, and easy-to-perform method to address questions regarding the function of genes, especially when hypomorphic knockdowns are needed. Therefore, effective transfection method with minimal side effects is essential for applying RNAi to hES cells. Here, we report a highly promising approach for targeted gene silencing in hES cells with siRNA complexed with cell-penetrating peptide PepFect 14 (PF14). This strategy provides researchers with efficient tool for unraveling the functions of genes or addressing the differentiation of pluripotent stem cells. Methods We present a method for delivery of siRNA into hES cells with cell-penetrating peptide PF14. Accordingly, hES cells were transfected in ROCK inhibitor containing medium for 24 h right after EDTA passaging as small cell clumps. Fluorescently labeled siRNA and siRNAs targeting OCT4 or beta-2-microglobulin (B2M) mRNA sequences were used to evaluate the efficiency of transfection and silencing. Analyses were performed at various time points by flow cytometry, RT-qPCR, and immunofluorescence microscopy. Results Effective downregulation of OCT4 in 70% of treated hES cells at protein level was achieved, along with 90% reduction at mRNA level in bulk population of cells. The applicability of this low-cost and easy-to-perform method was confirmed by inducing silencing of another target not associated with hES cell pluripotency (B2M). Furthermore, we discovered that downregulation of OCT4 induces neuroectodermal differentiation accompanied by reduced expression of B2M during early stage of this lineage. Conclusions The results demonstrate PF14 as a promising tool for studying gene function and regulatory networks in hES cells by using RNAi. |
| نوع الوثيقة: | article |
| وصف الملف: | electronic resource |
| اللغة: | English |
| تدمد: | 1757-6512 |
| Relation: | http://link.springer.com/article/10.1186/s13287-019-1144-x; https://doaj.org/toc/1757-6512 |
| DOI: | 10.1186/s13287-019-1144-x |
| URL الوصول: | https://doaj.org/article/50205bb260684d2cbb3e422b4eefcc20 |
| رقم الأكسشن: | edsdoj.50205bb260684d2cbb3e422b4eefcc20 |
| قاعدة البيانات: | Directory of Open Access Journals |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 17576512 |
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| DOI: | 10.1186/s13287-019-1144-x |