首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Biodentine and Mineral Trioxide Aggregate Induce Similar Cellular Responses in a Fibroblast Cell Line
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Biodentine and Mineral Trioxide Aggregate Induce Similar Cellular Responses in a Fibroblast Cell Line

机译:Biodentine和三氧化二矿物质总量在成纤维细胞系中诱导相似的细胞反应

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Introduction The aim of this study was to assess the cell viability and messenger RNA expression of interleukin (IL)-1α and IL-6 in 3T3 fibroblast cells when in direct contact with Biodentine (Septodont, Saint Maur de Fossés, France) and mineral trioxide aggregate (MTA). Methods Biodentine and MTA were coated onto coverslips and allowed to set. An uncoated coverslip and one coated with GC Fuji IX (GC Corporation, Tokyo, Japan) were used as controls. Coverslips were cultured with 3T3 fibroblast cells. Cell viability was assessed quantitatively using AlamarBlue dye (Serotec, Oxford, UK) after 3, 6, 24, and 72 hours. Morphologic cell changes of 3T3 cells in contact with BD and MTA were observed by scanning electron microscopy, and cytokine expression was assessed at the messenger RNA level by semiquantitative reverse-transcription polymerase chain reaction after 3 and 24 hours of direct contact with the materials. Results Cells in contact with Biodentine and MTA showed similar viability to untreated control cells at all time points, with the exception of 6 hours when viability was decreased with both treatments. Examination by scanning electron microscopy revealed cells adhering to most of the Biodentine surface after 24 hours. However, for MTA samples, significantly fewer cells were observed. The messenger RNA expression of IL-1α and IL-6 by cells in contact with Biodentine was similar to cells in contact with MTA. Conclusions Biodentine and MTA showed similar cytotoxicity and induced a similar pattern of cytokine expression.
机译:引言这项研究的目的是评估与Biodentine(Septodont,Saint Maur deFossés,法国)和三氧化二矿直接接触时3T3成纤维细胞中白细胞介素(IL)-1α和IL-6的细胞活力和信使RNA表达。聚合(MTA)。方法将Biodentine和MTA涂在盖玻片上并使其固化。将未涂覆的盖玻片和涂覆有GC Fuji IX(日本东京的GC公司)的盖玻片用作对照。盖玻片用3T3成纤维细胞培养。在3、6、24和72小时后,使用AlamarBlue染料(英国牛津的Serotec)定量评估细胞活力。通过扫描电子显微镜观察与BD和MTA接触的3T3细胞的形态学细胞变化,并在与材料直接接触3和24小时后,通过半定量逆转录聚合酶链反应在信使RNA水平评估细胞因子的表达。结果与Biodentine和MTA接触的细胞在所有时间点均显示出与未经处理的对照细胞相似的生存力,但两种处理均降低了6小时的生存能力。通过扫描电子显微镜检查发现24小时后细胞粘附在大部分Biodentine表面上。但是,对于MTA样品,观察到的细胞明显较少。与Biodentine接触的细胞IL-1α和IL-6的信使RNA表达与与MTA接触的细胞相似。结论Biodentine和MTA表现出相似的细胞毒性,并诱导相似的细胞因子表达模式。

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