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Cell survival and gene expression under compressive stress in a three-dimensional in vitro human periodontal ligament-like tissue model

机译:三维体外人牙周膜样组织模型中压应力下的细胞存活和基因表达

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摘要

This study investigated cell survival and gene expression under various compressive stress conditions mimicking orthodontic force by using a newly developed in vitro model of human periodontal ligament-like tissue (HPdLLT). The HPdLLT was developed by three-dimensional culturing of human periodontal ligament fibroblasts in a porous poly-l-lactide matrix with threefold increased culture media permeability due to hydrophilic modification. In vitro HPdLLTs in experimental groups were subjected to 5, 15, 25 and 35?g/cm2 compressive stress for 1, 3, 7 or 14?days; controls were cultured over the same periods without compressive stress. Cell morphology and cell apoptosis in the experimental and control groups were investigated using scanning electron microscopy and caspase-3/7 detection. Real-time polymerase chain reaction was performed for seven osteogenic and osteoclastic genes. Similar extracellular matrix and spindle-shaped cells were observed inside or on the surface of in vitro HPdLLTs, with no relation to compressive stress duration or intensity. Similar caspase-3/7 activity indicating comparable apoptosis levels was observed in all samples. Receptor activator of nuclear factor kappa-B ligand and bone morphogenetic protein 2 genes showed characteristic “double-peak” expression at 15 and 35?g/cm2 on day 14, and alkaline phosphatase and periodontal ligament-associated protein 1 expression peaked at 5?g/cm2 on day 14; other genes also showed time-dependent and load-dependent expression patterns. The in vitro HPdLLT model system effectively mimicked the reaction and gene expression of the human periodontal ligament in response to orthodontic force. This work provides new information on the effects of compressive stress on human periodontal ligament tissue.
机译:这项研究通过使用新开发的人牙周膜韧带样组织(HPdLLT)体外模型研究了在模拟正畸力的各种压应力条件下的细胞存活和基因表达。 HPdLLT是通过在亲水性改性的三倍增加的培养基渗透性的多孔聚丙交酯基质中对人牙周膜成纤维细胞进行三维培养而开发的。实验组的体外HPdLLTs受到5、15、25和35?g / cm2的压缩应力,持续1、3、7或14?天;对照在相同时期内培养而没有压应力。使用扫描电子显微镜和caspase-3 / 7检测研究实验组和对照组的细胞形态和细胞凋亡。对七个成骨和破骨基因进行了实时聚合酶链反应。在体外HPdLLT的内部或表面观察到类似的细胞外基质和纺锤形细胞,与压应力持续时间或强度无关。在所有样品中均观察到类似的caspase-3 / 7活性,表明可比较的凋亡水平。核因子κB配体和骨形态发生蛋白2基因的受体激活剂在第14天表现出特征性的“双峰”表达,分别为15和35?g / cm2,碱性磷酸酶和牙周膜相关蛋白1的表达达到峰值5?。第14天为g / cm2;其他基因也显示出时间依赖性和负荷依赖性表达模式。体外HPdLLT模型系统有效地模拟了响应正畸力的人类牙周膜的反应和基因表达。这项工作提供了有关压应力对人牙周膜组织的影响的新信息。

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