Department of Orthodontics, University of Regensburg, 93047 Regensburg, Germany.
Department of Biomaterials, University of Uberaba, Uberaba 38010-200, Brazil.
Int J Mol Sci. 2022 Dec 15;23(24):15948. doi: 10.3390/ijms232415948.
This study aimed to evaluate if single-nucleotide polymorphisms (SNPs) in the vitamin D receptor (VDR) gene are associated with gene expression in human periodontal ligament (hPDL) fibroblasts under simulated orthodontic compressive force. hPDL samples from 57 patients were used. A physiological compressive strain was performed to simulate orthodontic tooth movement in pressure areas under cell culture conditions. The RNA from hPDL fibroblasts was isolated to determine the relative gene expression (mRNA) of the VDR. The DNA was also isolated for the genotyping analysis of five SNPs in the VDR gene: BglI (rs739837, G/T), BsmI (rs1544410, T/C), ApaI (rs7975232, A/C), FokI (rs2228570, A/G), and TaqI (rs731236, A/G). Real-time polymerase chain reaction was used for both analyses. Kruskal−Wallis tests were used to compare VDR expression among genotypes of each SNP. A linear regression analysis was performed to evaluate SNP−SNP interaction. An established alpha of 5% was used. The relative mRNA VDR expression according to the genotypes in the SNPs BglI, BsmI, ApaI, FokI, and TaqI was not statistically significantly different (p > 0.05). The SNP−SNP interaction evaluated by regression analysis did not demonstrate any statistically significant association. No association was observed (p > 0.05). In conclusion, the SNPs BglI (rs739837), BsmI (rs1544410), ApaI (rs7975232), FokI (rs2228570), and TaqI (rs731236) did not show an impact on VDR gene expression in hPDL fibroblasts under simulated orthodontic compressive force.
本研究旨在评估维生素 D 受体(VDR)基因中的单核苷酸多态性(SNP)是否与模拟正畸压力下人类牙周韧带(hPDL)成纤维细胞中的基因表达相关。使用了 57 名患者的 hPDL 样本。在细胞培养条件下的压力区,通过生理压缩应变来模拟正畸牙齿移动。分离 hPDL 成纤维细胞的 RNA,以确定 VDR 的相对基因表达(mRNA)。还分离了 DNA 以进行 VDR 基因中五个 SNP 的基因分型分析:BglI(rs739837,G/T)、BsmI(rs1544410,T/C)、ApaI(rs7975232,A/C)、FokI(rs2228570,A/G)和 TaqI(rs731236,A/G)。Real-time polymerase chain reaction 用于这两种分析。Kruskal−Wallis 检验用于比较每个 SNP 基因型的 VDR 表达。进行线性回归分析以评估 SNP-SNP 相互作用。使用既定的 5%的 alpha 值。根据 BglI、BsmI、ApaI、FokI 和 TaqI 中 SNP 的基因型,VDR 相对 mRNA 表达在统计学上无显著差异(p>0.05)。通过回归分析评估的 SNP-SNP 相互作用没有显示出任何统计学上的关联。没有观察到关联(p>0.05)。总之,在模拟正畸压力下,BglI(rs739837)、BsmI(rs1544410)、ApaI(rs7975232)、FokI(rs2228570)和 TaqI(rs731236)SNP 对 hPDL 成纤维细胞中的 VDR 基因表达没有影响。