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骨原细胞对铝酸钙基水泥的反应。

Osteogenic cell response to calcium aluminate-based cement.

机构信息

School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.

School of Dentistry, University of Ribeirão Preto, Ribeirão Preto, SP, Brazil.

出版信息

Int Endod J. 2017 Aug;50(8):771-779. doi: 10.1111/iej.12682. Epub 2016 Sep 29.

Abstract

AIM

To evaluate the effect of a calcium aluminate-based cement (CAC+) on the development of the osteogenic phenotype in vitro.

METHODOLOGY

Rat calvaria-derived cells were grown on Thermanox coverslips for 24 h and then exposed to either samples (4-h set) of CAC+ or mineral trioxide aggregate (MTA) placed on Transwell inserts for periods of up to 14 days. Nonexposed cultures were used as the controls. The comparisons were made using the nonparametric Kruskal-Wallis test, followed by the Student-Newman-Keuls post hoc test when appropriate.

RESULTS

The results showed that proximity to MTA or CAC+ samples inhibited cell growth, whereas at a distance, viable and proliferative cells adhered to and spread on the Thermanox , expressing osteoblast differentiation markers prior to mineralization of the extracellular matrix. Compared with MTA, the osteogenic cell cultures exposed to CAC+ exhibited significantly greater cell viability, alkaline phosphatase (ALP) activity and expression of runt-related transcription factor 2, osterix, ALP, bone sialoprotein and osteocalcin (P < 0.05 for all). For the osteogenic cell cultures exposed to CAC+, the quantification of matrix mineralization was not altered (P > 0.05).

CONCLUSIONS

CAC+ supported the acquisition of the osteogenic cell phenotype in vitro, rendering this novel material a potential alternative to MTA in endodontic procedures. Further in vivo studies are needed to verify if the beneficial in vitro effects of CAC+ on osteoblastic cells correspond to an increase and/or acceleration of bone repair in the periapical region.

摘要

目的

评估铝酸钙基水泥(CAC+)对体外成骨表型发展的影响。

方法

将大鼠颅盖骨来源的细胞在 Thermanox 盖玻片上培养 24 小时,然后将其暴露于 CAC+或三氧化矿物凝聚体(MTA)的样本(4 小时组)置于 Transwell 插入物上,培养时间长达 14 天。未暴露的培养物用作对照。使用非参数 Kruskal-Wallis 检验进行比较,然后在适当的情况下使用 Student-Newman-Keuls 事后检验。

结果

结果表明,接近 MTA 或 CAC+样本会抑制细胞生长,而在远处,存活和增殖的细胞会附着并在 Thermanox 上扩散,在细胞外基质矿化之前表达成骨细胞分化标志物。与 MTA 相比,暴露于 CAC+的成骨细胞培养物表现出显著更高的细胞活力、碱性磷酸酶(ALP)活性和 runt 相关转录因子 2、osterix、ALP、骨唾液蛋白和骨钙素的表达(所有 P<0.05)。对于暴露于 CAC+的成骨细胞培养物,基质矿化的定量没有改变(P>0.05)。

结论

CAC+支持体外获得成骨细胞表型,使这种新型材料成为牙髓治疗中替代 MTA 的潜在选择。需要进一步的体内研究来验证 CAC+对成骨细胞的有益体外作用是否对应于根尖周区域骨修复的增加和/或加速。

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