Girija Kottuppallil, Kavitha Mahendran
Department of Conservative Dentistry and Endodontics, Tamil Nadu Government Dental College and Hospital, Tamil Nadu Dr. M.G.R Medical University, Chennai, Tamil Nadu, India.
J Conserv Dent. 2020 Jul-Aug;23(4):354-358. doi: 10.4103/JCD.JCD_3_20. Epub 2021 Jan 16.
The purpose of this study was to investigate the effects of platelet-rich fibrin (PRF) modified with bioactive radiopacifiers-nanohydroxyapatite (nHA) and dentin chips (DC) on odontoblastic differentiation in human dental pulp cells (HDPCs).
PRF was modified with 50wt% of nHA (G bone-SHAG31, Surgiwear Company) and 50 wt% of DC. HDPSCs differentiation and mineralization by the groups ([Group A - Control (Dimethyl sulfoxide), Group B - PRF, Group C - PRF + nHA, Group D - PRF + DC]) were assessed. ELISA was done to quantify the interleukin (IL)-6 and IL-8 cytokine expression. The odontoblastic differentiation was determined by the expression of odontogenesis-related genes and the extent of mineralization using alizarin red S staining.
One-way ANOVA with Tukey-honestly significant difference tests were applied to assess the significance among various groups.
The level of inflammatory cytokines (IL-6 and IL-8) expression by Group D (PRF + 50 wt% DC) was higher compared to Group B (PRF) and Group C (PRF + 50 wt% DC). Group C (PRF + 50 wt% nHA) induced more mineralization nodules compared to other groups. The integrated density value for the DSPP and DMP-1 protein expression by Group C (PRF + 50 wt% nHA) and Group D (PRF + 50 wt% DC) was higher compared to Group B (PRF).
The results suggest that the addition of bioactive radiopacifiers into PRF has a synergistic effect on the stimulation of odontoblastic differentiation of HDPCs, hence inducing mineralization.
本研究旨在探讨用生物活性显影剂——纳米羟基磷灰石(nHA)和牙本质碎屑(DC)改性的富血小板纤维蛋白(PRF)对人牙髓细胞(HDPCs)成牙本质细胞分化的影响。
用50wt%的nHA(G骨-SHAG31,外科手术用品公司)和50wt%的DC对PRF进行改性。评估各实验组([A组 - 对照组(二甲基亚砜),B组 - PRF,C组 - PRF + nHA,D组 - PRF + DC])对HDPSCs分化和矿化情况。采用酶联免疫吸附测定(ELISA)法对白细胞介素(IL)-6和IL-8细胞因子表达进行定量分析。通过成牙本质相关基因的表达以及使用茜素红S染色法测定矿化程度来确定成牙本质细胞分化情况。
采用单因素方差分析和Tukey真实显著性差异检验来评估各实验组之间的显著性差异。
与B组(PRF)和C组(PRF + 50wt% nHA)相比,D组(PRF + 50wt% DC)的炎性细胞因子(IL-6和IL-8)表达水平更高。与其他组相比,C组(PRF + 50wt% nHA)诱导产生的矿化结节更多。与B组(PRF)相比,C组(PRF + 50wt% nHA)和D组(PRF + 50wt% DC)的牙本质涎磷蛋白(DSPP)和牙本质基质蛋白-1(DMP-1)蛋白表达的积分密度值更高。
结果表明,向PRF中添加生物活性显影剂对刺激HDPCs的成牙本质细胞分化具有协同作用,从而诱导矿化。