Martín Gabriela, Preve Valentín, Hargreaves Kenneth, Diogenes Anibal, Inostroza Carolina, Saint-Jean Nicole, Brizuela Claudia
Department of Endodontics, Universidad Católica de Córdoba, Córdoba 5000, Argentina.
Faculty of Dentistry, Universidad Nacional de Córdoba, Córdoba 5000, Argentina.
Dent J (Basel). 2023 Sep 4;11(9):210. doi: 10.3390/dj11090210.
Regenerative endodontic procedures rely on the delivery of mesenchymal stem cells into the root canal and on the effect of local growth factors from the dentin and blood clot. The aim of this study was to assess the effect of dentin conditioning with ethylenediamine tetraacetic acid (EDTA) and diode lasers with different wavelengths (808 nm and 980 nm) on the expression of odontoblast-like cell markers. Forty dentin cylinders were divided into four groups according to the irrigation protocol: EDTA, EDTA + 808 nm diode laser, EDTA + 980 nm diode laser, and phosphate-buffered saline as the control group. Dental pulp stem cells were seeded into the previously conditioned cylinders and incubated for 14 days. The quantitative real-time polymerase chain reaction was used to evaluate the expression of dentin sialophosphoprotein (DSPP), dentin morphoprotein-1 (DMP-1), and transforming growth factor-beta 1 (TGF-β1). Data analysis was performed using the Kruskal-Wallis test. The activation of EDTA with 980 nm and 808 nm diode lasers resulted in lower DSPP and DMP-1 expression than that for EDTA alone ( < 0.05 and < 0.01, respectively). The expression of TGF was similar among all groups. The highest level of expression of odontoblast-like differentiation markers was observed with EDTA alone. However, the use of an 808 nm diode laser during EDTA irrigation reduced the expression of odontoblastic differentiation markers.
再生牙髓治疗程序依赖于将间充质干细胞输送到根管中,并依赖于来自牙本质和血凝块的局部生长因子的作用。本研究的目的是评估用乙二胺四乙酸(EDTA)和不同波长(808nm和980nm)的二极管激光处理牙本质对成牙本质样细胞标志物表达的影响。根据冲洗方案将40个牙本质圆柱体分为四组:EDTA组、EDTA + 808nm二极管激光组、EDTA + 980nm二极管激光组,以及作为对照组的磷酸盐缓冲盐水组。将牙髓干细胞接种到预先处理过的圆柱体中并孵育14天。采用定量实时聚合酶链反应来评估牙本质涎磷蛋白(DSPP)、牙本质形态蛋白-1(DMP-1)和转化生长因子-β1(TGF-β1)的表达。使用Kruskal-Wallis检验进行数据分析。与单独使用EDTA相比,980nm和808nm二极管激光激活EDTA后导致DSPP和DMP-1表达降低(分别为<0.05和<0.01)。所有组中TGF的表达相似。单独使用EDTA时观察到成牙本质样分化标志物的表达水平最高。然而,在EDTA冲洗过程中使用808nm二极管激光会降低成牙本质细胞分化标志物的表达。