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Improvement of osteogenesis in dental pulp pluripotent-like stem cells by oligopeptide-modified poly(beta-amino ester)s

机译:寡肽改性聚(β-氨基酯)改善牙科髓状多能干细胞中骨质发生的骨质发生

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摘要

Controlling pluripotent stem cell differentiation via genetic manipulation is a promising technique in regenerative medicine. However, the lack of safe and efficient delivery vehicles limits this application. Recently, a new family of poly(beta-amino ester)s (pBAEs) with oligopeptide-modified termini showing high transfection efficiency of both siRNA and DNA plasmid has been developed. In this study, oligopeptide-modified pBAEs were used to simultaneously deliver anti-OCT3/4 siRNA, anti-NANOG siRNA, and RUNX2 plasmid to cells from the dental pulp with pluripotent-like characteristics (DPPSC) in order to promote their osteogenic differentiation. Results indicate that transient inhibition of the pluripotency marker OCT3/4 and the overexpression of RUNX2 at day 7 of differentiation markedly increased and accelerated the expression of osteogenic markers. Furthermore, terminally-differentiated cells exhibited higher matrix mineralization and alkaline phosphatase activity. Finally, cell viability and genetic stability assays indicate that this co-delivery system has high chromosomal stability and minimal cytotoxicity. Therefore, we conclude that such co-delivery strategy is a safe and a quick option for the improvement of DPPSC osteogenic differentiation.
机译:通过遗传操纵控制多能干细胞分化是再生医学中有希望的技术。但是,缺乏安全高效的送货车限制了这一申请。最近,已经开发出具有寡肽改性的末端的多种聚(β-氨基酯)(PBAE),显示SiRNA和DNA质粒的高转染效率。在该研究中,使用寡肽改性的PBAES与具有多能特性(DPPSC)的牙髓纸浆同时递送抗-OT-10 / 4 siRNA,抗纳米siRNA和RONX2质粒,以促进其成骨分化。结果表明,分化的第7天在第7天在第7天的多能性标志物的瞬态抑制和Runx2的过表达显着增加,加速了骨质发生标志物的表达。此外,终末分化的细胞表现出更高的基质矿化和碱性磷酸酶活性。最后,细胞活力和遗传稳定性测定表明该共递送系统具有高染色体稳定性和最小的细胞毒性。因此,我们得出结论,这种共同传递策略是一种安全的和快速选择,用于改善DPPSC骨质发生分化。

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