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脱矿牙本质基质的脂质体递送用于牙齿组织再生。

Liposomal Delivery of Demineralized Dentin Matrix for Dental Tissue Regeneration.

机构信息

1 Department of Oral and Biomedical Sciences, School of Dentistry, Cardiff University , Cardiff, United Kingdom .

2 Department of Biological and Medical Sciences, Oxford Brookes University , Oxford, United Kingdom .

出版信息

Tissue Eng Part A. 2018 Jul;24(13-14):1057-1065. doi: 10.1089/ten.TEA.2017.0419. Epub 2018 Feb 21.

Abstract

Current dental restorations have short longevity, and consequently, there is a need for novel tissue engineering strategies that aim to regenerate the dentin-pulp complex. Dentin matrix contains a myriad of bioactive growth factors and extracellular matrix proteins associated with the recruitment, proliferation, and differentiation of dental pulp progenitor cells. In this study, we show that demineralized dentin matrix (DDM), from noncarious dentine, can be encapsulated into liposomes for delivery to dental tissue to promote regeneration. Liposomes were formulated to encapsulate 0-100 μg/mL DDM, lysed with Triton X, and used in vascular endothelial growth factor (VEGF) and transforming growth factor-β1 (TGF-β1) enzyme-linked immunosorbent assays to quantify release. The encapsulation efficiencies were calculated to be 25.9% and 28.8% (VEGF/TGF-β1) for 50 μg/mL DDM liposomes and 39% and 146.7% (VEGF/TGF-β1) for 100 μg/mL DDM liposomes. All liposome formulations had no cytotoxic effects on a dental pulp stem cell (DPSC) clone, as shown by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltertrazolium bromide), Caspase 3/7 assays, and cell counts. The ability of the liposomes to stimulate DPSC chemotactic recruitment was tested by Boyden chamber chemotaxis assays. Unloaded liposomes alone stimulated significant progenitor cell recruitment, while DDM-loaded liposomes further promoted chemotactic recruitment in a dose-dependent manner. DDM liposomes promoted the upregulation of "osteodentin" markers osteocalcin and RUNX2 (Runt-related transcription factor 2) in DPSCs after 9 days of treatment, determined by real-time quantitative PCR. Furthermore, Alizarin Red S staining showed that unloaded liposomes alone induced biomineralization of DPSCs, and DDM liposomes further increased the amount of mineralization observed. DDM liposomes were more effective than free DDM (10 μg/mL) at activating recruitment and osteogenic differentiation of DPSC, which are key events in the endogenous repair of the dentin-pulp complex. The study has highlighted the therapeutic potential of bioactive DDM liposomes in activating dental tissue repair in vitro, suggesting that liposomal delivery from biomaterials could be a valuable tool for reparative dentistry and hard-tissue engineering applications.

摘要

目前的牙科修复体寿命较短,因此需要新的组织工程策略来再生牙本质牙髓复合体。牙本质基质中含有许多与牙髓祖细胞的募集、增殖和分化相关的生物活性生长因子和细胞外基质蛋白。在这项研究中,我们表明,脱矿牙本质基质(DDM)可以封装在脂质体中,递送到牙齿组织中,以促进再生。脂质体被制成可以封装 0-100μg/mL 的 DDM,用 Triton X 裂解,并用于血管内皮生长因子(VEGF)和转化生长因子-β1(TGF-β1)酶联免疫吸附测定中,以定量释放。对于 50μg/mL 的 DDM 脂质体,包封效率分别为 25.9%和 28.8%(VEGF/TGF-β1),对于 100μg/mL 的 DDM 脂质体,包封效率分别为 39%和 146.7%(VEGF/TGF-β1)。所有脂质体配方对牙髓干细胞(DPSC)克隆均无细胞毒性作用,这通过 MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐)、Caspase 3/7 测定和细胞计数证明。通过 Boyden 室趋化性测定测试了脂质体刺激 DPSC 趋化性募集的能力。未负载的脂质体本身就刺激了显著的祖细胞募集,而负载 DDM 的脂质体则以剂量依赖的方式进一步促进了趋化性募集。通过实时定量 PCR 测定,DDM 脂质体在处理 9 天后还促进了 DPSCs 中“骨牙本质”标志物骨钙素和 RUNX2(Runt 相关转录因子 2)的上调。此外,茜素红 S 染色显示,未负载的脂质体本身诱导了 DPSCs 的生物矿化,而 DDM 脂质体进一步增加了观察到的矿化量。DDM 脂质体比游离 DDM(10μg/mL)更有效地激活 DPSCs 的募集和成骨分化,这是牙本质牙髓复合体内源性修复的关键事件。该研究强调了生物活性 DDM 脂质体在体外激活牙齿组织修复的治疗潜力,表明生物材料的脂质体递送可能是修复牙科和硬组织工程应用的有价值工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d5/6033301/f68b56c95b5c/fig-1.jpg

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