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首页> 外文期刊>Brazilian Dental Journal >Influence of Poly-L-Lactic Acid Scaffold's Pore Size on the Proliferation and Differentiation of Dental Pulp Stem Cells
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Influence of Poly-L-Lactic Acid Scaffold's Pore Size on the Proliferation and Differentiation of Dental Pulp Stem Cells

机译:聚乳酸支架孔大小对牙髓干细胞增殖和分化的影响

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The aim of this study was to evaluate the influence of the poly-L-lactic acid (PLLA)-based scaffold's pore size on the proliferation and differentiation of dental pulp stem cells (DPSCs). The scaffolds were prepared in pulp chambers of 1-mm-thick tooth slices from third molars using salt crystals (150-250 µm or 251-450 µm) as porogen. DPSC (1x105 cells) were seeded in the scaffolds with different pore sizes, and cultured in 24-well plates. The cell proliferation was evaluated using the WST-1 assay after 3-21 days. Furthermore, RT-PCR was used to assess the differentiation of the DPSCs into odontoblasts, using markers of odontoblastic differentiation (DSPP, DSP-1 and MEPE). RNA from human odontoblasts was used as control. Cell proliferation rate was similar in both scaffolds except at the 14th day period, in which the cells seeded in the scaffolds with larger pores showed higher proliferation (p0.05). After 21 days DPSCs seeded in both evaluated scaffolds were able of expressing odontoblastic markers DMP-1, DSPP and MEPE. In summary, both scaffolds tested in this study allowed the proliferation and differentiation of DPSCs into odontoblast-like cells.
机译:这项研究的目的是评估基于聚L-乳酸(PLLA)的支架的孔径对牙髓干细胞(DPSCs)增殖和分化的影响。使用盐晶体(150-250 µm或251-450 µm)作为成孔剂,在第1磨牙的1毫米厚的牙切片的牙髓腔中制备支架。将DPSC(1x105细胞)接种在具有不同孔径的支架中,并在24孔板中培养。 3-21天后,使用WST-1测定法评估细胞增殖。此外,RT-PCR用于评估成牙本质细胞分化的标志物(DSPP,DSP-1和MEPE),将DPSC分化为成牙本质细胞。来自人成牙本质细胞的RNA用作对照。除了在第14天时,两种支架上的细胞增殖速率都相似,在第14天期间,接种在具有较大孔的支架上的细胞显示出更高的增殖(p <0.05)。 21天后,在两种评估的支架中接种的DPSC能够表达牙母细胞标记物DMP-1,DSPP和MEPE。总之,在这项研究中测试的两个支架都允许DPSC增殖和分化为成牙本质细胞样细胞。

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