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富含血小板纤维蛋白、富含血小板纤维蛋白+50重量%纳米羟基磷灰石、富含血小板纤维蛋白+50重量%牙本质碎屑对成牙本质细胞分化的比较评价——一项研究的第2部分。

Comparative evaluation of platelet-rich fibrin, platelet-rich fibrin + 50 wt% nanohydroxyapatite, platelet-rich fibrin + 50 wt% dentin chips on odontoblastic differentiation - An study-part 2.

作者信息

Girija Kottuppallil, Kavitha Mahendran

机构信息

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.

出版信息

J Conserv Dent. 2020 Jul-Aug;23(4):354-358. doi: 10.4103/JCD.JCD_3_20. Epub 2021 Jan 16.

Abstract

AIM

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).

SUBJECTS AND METHODS

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.

STATISTICAL ANALYSIS USED

One-way ANOVA with Tukey-honestly significant difference tests were applied to assess the significance among various groups.

RESULTS

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).

CONCLUSIONS

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.

摘要

目的

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。

对象与方法

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。

统计分析方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0cd/7883785/35f3e775173d/JCD-23-354-g001.jpg

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