负载转化生长因子 β1 的脂质体促进牙髓干细胞的牙源性分化。
Liposomes loaded with transforming growth factor β1 promote odontogenic differentiation of dental pulp stem cells.
机构信息
Department of Paediatric Dentistry, School of Stomatology, China Medical University, Shenyang, China; Department of Oral and Biomedical Sciences, School of Dentistry, Cardiff University, Cardiff, UK.
Department of Oral and Biomedical Sciences, School of Dentistry, Cardiff University, Cardiff, UK; Cardiff Institute for Tissue Engineering and Repair (CITER), Cardiff, UK.
出版信息
J Dent. 2020 Dec;103:103501. doi: 10.1016/j.jdent.2020.103501. Epub 2020 Oct 14.
OBJECTIVES
This study investigated whether novel liposome formulations loaded with transforming growth factor β1 (TGF-β1) could promote the odontogenic differentiation of human dental pulp stem cells (hDPSCs) for dentine-pulp regeneration.
METHODS
0-100 ng/mL of liposomal TGF-β1 was prepared using the thin-film hydration method. Release of TGF-β1 from the liposomes was quantified by an enzyme-linked immunosorbent assay (ELISA). The hDPSCs were treated with different concentrations of liposomal TGF-β1 and cell viability was tested using an MTT assay. "Osteodentine" differentiation capacity was assessed by RT-qPCR, ELISA and Alizarin red S staining.
RESULTS
The ELISA results showed that liposomal TGF-β1 achieved a controlled and prolonged release over time. The MTT results demonstrated that the liposomes (100 μg/mL) were not cytotoxic to the cells. Liposomal TGF-β1 up-regulated the expression of "osteodentine" markers, RUNX-2, DMP-1 and DSPP, in hDPSCs after 7 days of treatment and resulted in the accumulation of mineralised nodules.
CONCLUSION
This study indicated that liposomes are an effective carrier for delivering TGF-β1 over time. Liposomal TGF-β1 promoted dentinogenesis and increased mineralisation in hDPSCs. This highlights the potential of liposomal TGF-β1 for future use in dentine-pulp regeneration.
CLINICAL SIGNIFICANCE
Liposomal TGF-β1 may be used as a synergist for promoting dentine-pulp regeneration of immature permanent teeth or as a pulp capping agent for inducing reparative dentine formation.
目的
本研究旨在探讨新型载转化生长因子β1(TGF-β1)脂质体能否促进人牙髓干细胞(hDPSCs)牙本质-牙髓再生的牙向分化。
方法
采用薄膜水化法制备 0-100ng/mL 的脂质体 TGF-β1,并通过酶联免疫吸附试验(ELISA)定量检测 TGF-β1 的释放。用不同浓度的脂质体 TGF-β1 处理 hDPSCs,通过 MTT 试验检测细胞活力。通过 RT-qPCR、ELISA 和茜素红 S 染色评估“类牙骨质”分化能力。
结果
ELISA 结果表明,脂质体 TGF-β1 可实现时间依赖性的控制和缓释。MTT 结果表明,脂质体(100μg/mL)对细胞无细胞毒性。脂质体 TGF-β1 可上调 hDPSCs 中“类牙骨质”标志物 RUNX-2、DMP-1 和 DSPP 的表达,并在 7 天治疗后导致矿化结节的积累。
结论
本研究表明,脂质体是一种有效的 TGF-β1 递药载体,可实现时间依赖性缓释。脂质体 TGF-β1 可促进 hDPSCs 牙骨质形成,并增加矿化。这突出了脂质体 TGF-β1 在未来用于牙本质-牙髓再生的潜力。
临床意义
脂质体 TGF-β1 可作为协同剂促进未成熟恒牙牙本质-牙髓再生,或作为牙髓盖髓剂诱导修复性牙本质形成。