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成牙骨质细胞对基于磷酸钙树脂和硅酸钙的商用封闭剂的反应。

The response of cementoblasts to calcium phosphate resin-based and calcium silicate-based commercial sealers.

机构信息

Department of Periodontology, Selcuk University, Konya, Turkey.

出版信息

Int Endod J. 2013 Mar;46(3):242-52. doi: 10.1111/j.1365-2591.2012.02122.x. Epub 2012 Sep 24.

Abstract

AIM

To investigate cell viability and gene expression of cementoblasts (OCCM.30) exposed to extractable components released by resin-based sealers with different chemical composition Hybrid Root Seal (HRS), SimpliSeal (SS), Real Seal (RS) and AH Plus (AH) and by a MTA-based sealers Tech Biosealer Endo (TBE).

METHODOLOGY

Discs of all materials were prepared and allowed to set in humid conditions at 37° for 48 h. The discs were then incubated for 72 h at 37 °C to obtain material extracts (1/1) in DMEM. The extracts containing the components released by the sealers were filtered and other dilutions (1/2, 1/4) were prepared from the original solution (1/1). Original and diluted solutions were tested on the cementoblasts. Impedance-based real-time cell analysis (RTCA) was used to evaluate cell viability, quantitative real-time polymerase chain reaction (QRT-PCR) was used to examine the expression of mineralization-related genes (osteocalcin; OCN, Runt-related transcription factor-2; Runx2, collagen type 1; COL I, alkaline phosphatase; ALP). For statistical analysis, one-way analysis of variance (anova) and Tukey's honestly significant difference (HSD) tests were used.

RESULTS

TBE (1/2), RS (1/2, 1/4), and HRS (1/2, 1/4) significantly decreased cell viability (P < 0.001). AH (1/2, 1/4) and SS (1/2, 1/4) had similar cell viability to the control at 30 h. All tested materials significantly decreased cell viability when compared to the control group except AH (1/2, 1/4) and SS (1/4) at 90 h. All of the tested sealers reduced COL I mRNA expressions when compared to the control. SS was associated with significant increases in OCN and Runx2 mRNA expressions when compared to the control (P < 0.001). Whereas all of the dilutions of TBE, RS and HRS significantly decreased BSP mRNA expressions (P < 0,001), 1/2 and 1/4 dilutions of SS increased BSP mRNA expression (P < 0,001). Except the 1/4 dilutions of AH and SS, all the sealer dilutions significantly reduced ALP mRNA expression in cementoblasts (P < 0,001).

CONCLUSIONS

SimpliSeal and AH Plus resulted in more favourable response to cementoblasts because of their regulation potential on the mineralized tissue-associated protein's mRNA expressions.

摘要

目的

研究不同化学成分的树脂基密封剂(Hybrid Root Seal [HRS]、SimpliSeal [SS]、Real Seal [RS] 和 AH Plus [AH])和基于 MTA 的密封剂 Tech Biosealer Endo(TBE)释放的可提取成分对成牙骨质细胞(OCCM.30)活力和基因表达的影响。

方法

制备所有材料的圆盘,并在 37°C 的潮湿条件下放置 48 小时以使其凝固。然后将圆盘在 37°C 下孵育 72 小时,以获得 DMEM 中的材料提取物(1/1)。过滤含有密封剂释放成分的提取物,并从原始溶液(1/1)中制备其他稀释液(1/2、1/4)。将原始溶液和稀释溶液用于成牙骨质细胞。基于阻抗的实时细胞分析(RTCA)用于评估细胞活力,实时定量聚合酶链反应(QRT-PCR)用于检测矿化相关基因(骨钙素;OCN、Runt 相关转录因子 2;Runx2、胶原蛋白 1;COL I、碱性磷酸酶;ALP)的表达。进行统计分析时,使用单因素方差分析(anova)和 Tukey 的显著差异(HSD)检验。

结果

TBE(1/2)、RS(1/2、1/4)和 HRS(1/2、1/4)显著降低细胞活力(P<0.001)。AH(1/2、1/4)和 SS(1/2、1/4)在 30 小时时与对照组的细胞活力相似。与对照组相比,所有测试材料均显著降低了细胞活力,除了 AH(1/2、1/4)和 SS(1/4)在 90 小时时。与对照组相比,所有测试密封剂均降低 COL I mRNA 表达。与对照组相比,SS 与 OCN 和 Runx2 mRNA 表达的显著增加相关(P<0.001)。然而,TBE、RS 和 HRS 的所有稀释液均显著降低 BSP mRNA 表达(P<0.001),SS 的 1/2 和 1/4 稀释液增加 BSP mRNA 表达(P<0.001)。除 AH 和 SS 的 1/4 稀释液外,所有密封剂稀释液均显著降低成牙骨质细胞中 ALP mRNA 表达(P<0.001)。

结论

由于 SimpliSeal 和 AH Plus 对矿化组织相关蛋白 mRNA 表达具有调节潜力,因此它们对成牙骨质细胞的反应更为有利。

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