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[关于包裹在泊洛沙姆F-127水凝胶中的牙髓干细胞体外成骨分化的实验研究]

[Experimental study on the in vitro osteogenic differentiation of dental pulp stem cells encapsulated in Pluronic F-127 hydrogel].

作者信息

Paerhati Abudureheman, Muhetaer Huojia, Duolikun Wufuer, Maimaitiyiming Halike, Liu X W

机构信息

Department of Stomatology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830001, China.

出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2016 Jul;51(7):420-5. doi: 10.3760/cma.j.issn.1002-0098.2016.07.009.

Abstract

OBJECTIVE

To evaluate the biocompatibility and viability of nonionic triblock copolymer Pluronic F-127 as a cell scaffold for osteogenic differentiation of dental pulp stem cells(DPSC).

METHODS

DPSC were obtained via enzymatic digestion method and purified bylimited dilution method. The freeze dried hydrogel of 20% Pluronic F-127 was prepared and itsstructurewas observed usingscanning electron microscopy(SEM). After the encapsulation of cells of passage 3 in Pluronic F-127, the effects of hydrogel on the proliferations of DPSC were assessed with methyl thiazolyl terazolium(MTT) after one day and 3, 5, 7 days of incubations, respectively. On day 14, osteogenic abilities of DPSC encapsulated in the hydrogel were estimated by means of alizarin red S, immunocytochemical staining and real-time quantitative PCR(RT-qPCR).

RESULTS

DPSC were isolated and cultured successfully in the present study. SEM observations showed that porous structures which might be suitable for cell culture. A570 values of MTT were then normalized. A570 values of the cells in 2D cultures were 0.30±0.06, 0.30±0.17, 0.35±0.04 and 0.25±0.06 and A570 values of DPSC in 3D cultures were 0.36±0.06, 0.54±0.18, 0.70±0.10 and 0.32±0.10 on day 1, 3, 5 and 7, respectively. A570 value peaks were found on day 5 in both groups. The proliferation of 3D cultured DPSC was higher than that of 2D cultured cells(P<0.05). After 14 days of osteogenic induction, there were no calcium nodules observed in the control group and the numbers of calcium nodulesin the 2D and 3D groups had no significant difference(P>0.05). Inmmunocytochemical staining demonstrated strong expression of osteoblast marker Runt-related transcription factor 2(RUNX2), type Ⅰ collagen(Col-Ⅰ) and relatively low expression of osteocalcin(OCN). Moreover, RT-qPCR showed no differences between the relative expression of ALP, RUNX-2, OCN in the 2D and 3D groups (P>0.05), but a higher relative expression of Col-Ⅰ was observed in the 3D group(P=0.023).

CONCLUSIONS

Pluronic F-127 is a promising cell scaffold or cell carrier for the osteobalst differentiation of dental pulp stem cells.

摘要

目的

评估非离子三嵌段共聚物普朗尼克F-127作为牙髓干细胞(DPSC)成骨分化细胞支架的生物相容性和活力。

方法

通过酶消化法获取DPSC,并采用有限稀释法进行纯化。制备20%普朗尼克F-127的冻干水凝胶,用扫描电子显微镜(SEM)观察其结构。将第3代细胞包封于普朗尼克F-127中后,分别在培养1天、3天、5天和7天后,用噻唑蓝(MTT)法评估水凝胶对DPSC增殖的影响。在第14天,通过茜素红S染色、免疫细胞化学染色和实时定量PCR(RT-qPCR)评估包封于水凝胶中的DPSC的成骨能力。

结果

本研究成功分离并培养了DPSC。SEM观察显示存在可能适合细胞培养的多孔结构。然后对MTT的A570值进行标准化。二维培养的细胞在第1天、3天、5天和7天的A570值分别为0.30±0.06、0.30±0.17、0.35±0.04和0.25±0.06,三维培养的DPSC在相应天数的A570值分别为0.36±0.06、0.54±0.18、0.70±0.10和0.32±0.10。两组在第5天均出现A570值峰值。三维培养的DPSC的增殖高于二维培养的细胞(P<0.05)。成骨诱导14天后,对照组未观察到钙结节,二维组和三维组的钙结节数量无显著差异(P>0.05)。免疫细胞化学染色显示成骨细胞标志物Runx相关转录因子2(RUNX2)、Ⅰ型胶原(Col-Ⅰ)表达较强,骨钙素(OCN)表达相对较低。此外,RT-qPCR显示二维组和三维组碱性磷酸酶(ALP)、RUNX-2、OCN的相对表达无差异(P>0.05),但三维组Col-Ⅰ的相对表达较高(P=0.023)。

结论

普朗尼克F-127是一种有前景的用于牙髓干细胞向成骨细胞分化的细胞支架或细胞载体。

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