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Passaging effects on mineralization and mRNA expression of rat calvarial cells seeded in monolayer and on 3D polymer constructs in vitro

机译:单层和3D聚合物构建体中大鼠颅骨细胞矿化和mRNA表达的传递对粒子钙细胞的表达

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In this study, primary rat calvarial cells were expanded and then seeded in monolayer and on porous 3D scaffolds to determine the effect of passaging on matrix mineralization and osteogenic gene mRNA production. Passage 1, 2 and 3 cells were seeded in collagen coated 6 well plates and on 5mm × 3mm poly(L-lactide-co-D, L-lactide 70:30) (PLDL) discs (n=6 for each group). Monolayer culture was carried out to 3 weeks and plates were stained by Von Kossa to measure mineralization area. Constructs were cultured for 8 weeks and scanned by micro-computed tomography (μCT) at 24 and 57 days to quantify mineralization. Both culture groups were analyzed with real-time quantitative RT-PCR to determine the amount of osteogenic gene mRNA produced. Von Kossa staining showed a statistically significant decrease in the amount of mineralized nodule formation as passage number increased. There was no significant difference in the amount of mineralization produced by each passage group in 3D culture as shown by ~LCT analysis. There was no reduction in osteogenic mRNA detected by real time quantitative RT-PCR for osteocalcin (OCN), osteopontin (OPN), osteonectin (ONN) or alkaline phosphatase (ALP) from passage 1 to 3 in 3D culture while 2D culture did show reductions in OCN and OPN with passaging.
机译:在这项研究中,原代大鼠颅盖细胞扩增,然后在单层和在多孔3D支架接种,以确定传代于基质矿化和成骨基因的mRNA产生的效果。通道1,2和3细胞胶原包被的6个孔板中,并于5毫米×3毫米聚(L-丙交酯 - 共 - d,L-丙交酯70:30)(PLDL)光盘(N = 6对于每个组)接种。单层培养物进行至3周,将板由冯科萨染色以测量矿化面积。构建体8周中培养,并在24和57天微计算机断层摄影(μCT)扫描量化矿化。两种培养基与实时定量RT-PCR进行分析以确定成骨基因的mRNA产生的量。冯Kossa染色表明在矿化结节形成的量的统计学显著减少作为通道数增加。有在矿化如图〜LCT分析通过在3D培养各通道组产生的量没有显著差异。有在成骨的mRNA不降低通过实时定量RT-PCR来自通道1在3D培养检测到骨钙素(OCN),骨桥蛋白(OPN),骨连接素(ONN)或碱性磷酸酶(ALP)到3,而2D培养确实显示减少在OCN和OPN与传代。

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