用于牙槽骨缺损再生和修复的 RNA 技术。

Journal of dental research Pub Date : 2024-06-01 Epub Date: 2024-05-07 DOI:10.1177/00220345241242047
D Su, S Swearson, S Eliason, K G Rice, B A Amendt
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引用次数: 0

摘要

microRNA-200a(miR-200a)靶向参与成骨分化和骨发育的多种信号通路。然而,它在成骨和骨再生中的治疗功能仍然未知。在本研究中,我们利用体外和体内模型研究了 miR-200a 过表达和使用基于质粒的 miR 抑制剂系统(PMIS)抑制 miR-200a 对成骨分化和骨再生的分子功能。利用PMIS-miR-200a抑制miR-200a能显著增加人胚胎腭间充质细胞的成骨生物标志物,并促进大鼠牙槽缺损的骨再生。在大鼠上颌 M1 磨牙拔除术中,用种植钻去除支撑牙齿的结构,在牙槽骨上形成 3 毫米的缺损。在打开的牙槽骨缺损中插入胶原蛋白海绵,并在海绵中加入 PMIS-miR-200a 质粒 DNA,然后缝合伤口以保护海绵并关闭缺损。重要的是要去除可能影响牙槽骨再生的现有牙齿支撑结构。牙槽骨在 4 周后再生。海绵胶原起到了稳定的作用,并将 PMIS-miR-200a DNA 传递给进入骨缺损海绵中的细胞。我们发现,表达 CD90 和 Stro-1 的间充质干细胞进入海绵,吸收 DNA 并表达 PMIS-miR-200a。PMIS-miR-200a 启动了体内转化细胞的骨再生程序。研究发现,体外抑制 miR-200a 能上调 Wnt 和 BMP 信号活性以及与成骨相关的 Runx2、OCN、Lef-1、Msx2 和 Dlx5。对 PMIS-miR-200a 处理过的大鼠进行的肝脏和血液毒性测试表明,几种肝病生物标志物没有增加。这些结果证明了 PMIS-miR-200a 在快速骨再生方面的治疗功能。此外,这些研究旨在证明 PMIS-miR-200a 溶液的易用性,在临床上使用注射器进行一次性简单应用即可。
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RNA Technology to Regenerate and Repair Alveolar Bone Defects.

microRNA-200a (miR-200a) targets multiple signaling pathways that are involved in osteogenic differentiation and bone development. However, its therapeutic function in osteogenesis and bone regeneration remains unknown. In this study, we use in vitro and in vivo models to investigate the molecular function of miR-200a overexpression and miR-200a inhibition using a plasmid-based miR inhibitor system (PMIS) on osteogenic differentiation and bone regeneration. Inhibition of miR-200a using PMIS-miR-200a significantly increased osteogenic biomarkers of human embryonic palatal mesenchyme cells and promoted bone regeneration in rat tooth socket defects. In rat maxillary M1 molar extractions, the supporting tooth structures were removed with an implant drill to yield a 3-mm defect in the alveolar bone. A collagen sponge was inserted into the open alveolar defect and PMIS-miR-200a plasmid DNA was added to the sponge and the wound sutured to protect the sponge and close the defect. It was important to remove the existing tooth supporting structure, which can influence alveolar bone regeneration. The alveolar bone was regenerated in 4 wk. The collagen sponge acts to stabilize and deliver the PMIS-miR-200a DNA to cells entering the sponge in the bone defect. We show that mesenchymal stem cells expressing CD90 and Stro-1 enter the sponges, take up the DNA, and express PMIS-miR-200a. PMIS-miR-200a initiates a bone regeneration program in transformed cells in vivo. In vitro inhibition of miR-200a was found to upregulate Wnt and BMP signaling activity as well as Runx2, OCN, Lef-1, Msx2, and Dlx5 associated with osteogenesis. Liver and blood toxicity testing of PMIS-miR-200a-treated rats showed no increase in several biomarkers of liver disease. These results demonstrate the therapeutic function of PMIS-miR-200a for rapid bone regeneration. Furthermore, the studies were designed to demonstrate the ease of use of PMIS-miR-200a in solution and applied using a syringe in the clinic through a simple one-time application.

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