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氟化物可调节前成骨细胞的活力以及基质金属蛋白酶-2和-9的活性。

Fluoride modulates preosteoblasts viability and matrix metalloproteinases-2 and -9 activities.

作者信息

Slompo Camila, Buzalaf Camila P, Damante Carla A, Martins Gisele M, Hannas Angélica R, Buzalaf Marília A R, Oliveira Rodrigo C

机构信息

Department of Biological Sciences, Bauru Dental School, USP - University of São Paulo, Bauru, SP, Brazil.

出版信息

Braz Dent J. 2012;23(6):629-34. doi: 10.1590/s0103-64402012000600002.

Abstract

This study evaluated the influence of fluoride on cell viability and activity of matrix metalloproteinases (MMP) -2 and -9 secreted by preosteoblasts. Preosteoblasts (MC3T3-E1 murine cell line) were cultured in MEM medium supplement with 10% Fetal Bovine Serum (FBS) and nucleosides/ribonucleosides without ascorbic acid. Adherent cells were treated with different concentrations of F (as sodium fluoride-NaF) in medium (5 x 10(-6) M, 10(-5) M, 10(-4) M and 10(-3) M) for 24, 48, 72 and 96 h at 37ºC, 5% CO(2). Control cells were cultivated in MEM only. After each period, preosteoblast viability was assessed by MTT assay. MMP-2 and -9 activities were performed by gel zymography. Also, alkaline phosphatase (ALP) activity was quantified by colorimetry in all experimental groups. It was shown that cultured cells with the highest dose of F (10(-3) M) for 96 h decreased preosteoblast viability while lower doses of F did not alter it, when compared to untreated cells. No differences were observed in ALP activity among groups. Moreover, compared to control, the treatment of cells with F at low dose slightly increased MMP-2 and -9 activities after 24 h. It was concluded that F modulates preosteoblast viability in a dose-dependent manner and also may regulate extracellular matrix remodeling.

摘要

本研究评估了氟对前成骨细胞分泌的基质金属蛋白酶(MMP)-2和-9的细胞活力及活性的影响。前成骨细胞(MC3T3-E1小鼠细胞系)在补充有10%胎牛血清(FBS)和核苷/核糖核苷且无抗坏血酸的MEM培养基中培养。贴壁细胞在37℃、5% CO₂条件下,于培养基中用不同浓度的氟(以氟化钠-NaF形式)(5×10⁻⁶ M、10⁻⁵ M、10⁻⁴ M和10⁻³ M)处理24、48、72和96小时。对照细胞仅在MEM中培养。每个时间段后,通过MTT法评估前成骨细胞活力。通过凝胶酶谱法检测MMP-2和-9的活性。此外,通过比色法对所有实验组的碱性磷酸酶(ALP)活性进行定量。结果显示,与未处理细胞相比,用最高剂量的氟(10⁻³ M)处理96小时的培养细胞降低了前成骨细胞活力,而较低剂量的氟未改变其活力。各实验组之间的ALP活性未观察到差异。此外,与对照组相比,低剂量氟处理细胞24小时后,MMP-2和-9的活性略有增加。得出的结论是,氟以剂量依赖的方式调节前成骨细胞活力,并且还可能调节细胞外基质重塑。

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