Vongsakulpaisarn Poranee, Sangkhamanee Sujiwan Seubbuk, Rassameemasmaung Supanee, Sritanaudomchai Hathaitip
Department of Oral Medicine and Periodontology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Department of Oral Biology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Eur J Dent. 2024 Feb;18(1):378-386. doi: 10.1055/s-0043-1771337. Epub 2023 Aug 10.
Tumor necrosis factor-α (TNF-α) causes bone resorption in periodontitis. It induces the production of receptor activator of NF-κB ligand (RANKL) from osteoblasts, leading to the disturbance of bone homeostasis through RANKL, RANK, and osteoprotegerin (OPG) axis. This study aimed to explore the effect of periodontal ligament stem cells-derived conditioned medium (PDLSCs-CM) on gene expression related to bone homeostasis and the differentiation of TNF-α-challenged osteoblasts.
Human osteoblasts were cultured with 50 ng/mL of TNF-α and 0, 1, 10, and 100 µg/ mL of PDLSCs-CM. Osteoblasts cultured without TNF-α and PDLSCs-CM were served as control. Gene expression of RANKL, OPG, and interleukin-1β (IL-1β) was evaluated by reverse transcription quantitative polymerase chain reaction at 48 hours. The early-stage and late-stage differentiation of TNF-α-challenged osteoblasts without or with PDLSCs-CM was explored by alkaline phosphatase (ALP) activity and alizarin red staining, respectively, at day 1, 3, 6, 9, and 12.
Mann-Whitney U test was used to analyze the differences in gene expression of TNF-α-challenged osteoblasts at 24 and 48 hours, and Kruskal-Wallis test was used to analyze the effect of PDLSCs-CM on gene expression and ALP activity among all experimental groups using SPSS software version 21.0. Statistical significance was considered with -value less than 0.05.
Expression of RANKL, OPG and IL-1β was significantly upregulated in TNF-α-challenged osteoblasts compared to the untreated control. The PDLSCs-CM at 1 and 10 μg/mL downregulated gene expression of TNF-α-challenged osteoblasts compared to the group without PDLSCs-CM, but the difference did not reach statistical significance. The ALP activity was decreased in TNF-α-challenged osteoblasts. The addition of PDLSCs-CM did not alter ALP activity of TNF-α-challenged osteoblasts. Alizarin red staining was comparable in the TNF-α-challenged osteoblasts cultured without or with PDLSCs-CM.
The PDLSCs-CM did not alter gene expression involved in bone homeostasis and differentiation of TNF-α-challenged osteoblasts.
肿瘤坏死因子-α(TNF-α)可导致牙周炎中的骨吸收。它诱导成骨细胞产生核因子κB受体激活蛋白配体(RANKL),通过RANKL、RANK和骨保护素(OPG)轴导致骨稳态紊乱。本研究旨在探讨牙周膜干细胞条件培养基(PDLSCs-CM)对与骨稳态相关基因表达及TNF-α刺激的成骨细胞分化的影响。
将人成骨细胞与50 ng/mL的TNF-α以及0、1、10和100 μg/mL的PDLSCs-CM一起培养。未用TNF-α和PDLSCs-CM培养的成骨细胞作为对照。在48小时时通过逆转录定量聚合酶链反应评估RANKL、OPG和白细胞介素-1β(IL-1β)的基因表达。分别在第1、3、6、9和12天通过碱性磷酸酶(ALP)活性和茜素红染色探索有无PDLSCs-CM的TNF-α刺激的成骨细胞的早期和晚期分化。
使用曼-惠特尼U检验分析TNF-α刺激的成骨细胞在24和48小时时基因表达的差异,使用Kruskal-Wallis检验分析PDLSCs-CM对所有实验组基因表达和ALP活性的影响,采用SPSS 21.0软件。P值小于0.05时认为具有统计学意义。
与未处理的对照相比,TNF-α刺激的成骨细胞中RANKL、OPG和IL-1β的表达显著上调。与无PDLSCs-CM的组相比,1和10 μg/mL的PDLSCs-CM下调了TNF-α刺激的成骨细胞的基因表达,但差异未达到统计学意义。TNF-α刺激的成骨细胞中ALP活性降低。添加PDLSCs-CM未改变TNF-α刺激的成骨细胞的ALP活性。在有无PDLSCs-CM培养的TNF-α刺激的成骨细胞中茜素红染色相当。
PDLSCs-CM未改变参与骨稳态及TNF-α刺激的成骨细胞分化的基因表达。