通过DNA四面体框架传递化学修饰的microRNA,用于牙髓再生
Xiaoling Wei1,2, Huaxing Xu1,2, Mengqi Zhou1,2
1Shanghai Stomatological Hospital and School of Stomatology, Fudan University, Shanghai, 200001, China.
Journal of nanobiotechnology
|April 4, 2024
概括
化学修饰的miRNA载入纳米结构有效地促进牙髓干细胞 (DPSC) 再生和血管生成. 这一突破增强了血管网络的形成,以改善牙组织工程和再生牙科应用.
科学领域:
- 恢复性牙科 恢复性牙科
- 生物材料科学 生物材料科学
- 组织工程是组织工程.
背景情况:
- 牙纸再生对于治疗牙疾病至关重要.
- 建立功能性血管网络与牙纸干细胞 (DPSCs) 是一个关键的挑战.
- 目前用于激活DPSC的方法缺乏效率和稳定性.
研究的目的:
- 开发一种用于增强DPSC介导血管生成和牙髓再生的新型纳米结构.
- 为了研究化学修饰的微RNA (miRNA) 装载的四面体DNA纳米结构 (miR@TDNs) 对于DPSC激活和传递的有效性.
主要方法:
- 合成化学修饰的miR-126-3p载荷四面体DNA纳米结构 (miR@TDNs).
- 在体外评估miR@TDNs对DPSC增殖,迁移和血管生成相关的基因表达的影响.
- 评估内皮细胞对增强的DPSC对神经信号传递的反应.
- 在体内验证使用matrigel插头测定和异胎牙肉质移植.
主要成果:
- miR@TDNs显著增强了DPSC的增殖,迁移和血管生成基因上调.
- 来自DPSCs的改善膜信号导致增强内皮细胞管的形成和迁移.
- 在体内研究证实,miR@TDNs促进血管生成,促进牙纸再生.
结论:
- 化学修饰的miRNA载核酸纳米结构有效增强DPSC介导的血管生成.
- 这种方法显示出促进牙纸再生的巨大潜力.
- 基于核酸的输送系统在再生牙科中是一个有前途的治疗策略.
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MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
