Yan Wu, Chao Deng, Kun Yang, Xiaoxia Cui, Qi Liu, Yan Jin
Hua Xi Kou Qiang Yi Xue Za Zhi. 2015 Dec;33(6):627-32. doi: 10.7518/hxkq.2015.06.016.
The effect of advanced glycation end products (AGEs) on the osteogenic differentiation of humanperiodontal ligament stem cells(hPDLSCs) was discussed. Changes in the Wnt signaling pathway during glycation were also determined.
In vitro tissue explanting method was primarily applied. Limiting diluted clone was cultured to obtain hPDLSCs in vitro. The subjects were divided into two groups: the healthy group (N-hPDLSCs) and the AGEs-stimulating group (A-hPDLSCs). Osteoblast mineralization was induced in the experimental groups. The following processes were performed: alizarin red staining; alkaline phosphatase (ALP) staining; real time polymerase chain reaction (real time PCR) for detecting osteogenic genes and Wnt classical pathway-related factors, DKK-1 and β-catenin; Western blot analysis. Bone protein and β-catenin were correlated in the nuclear expression.
The cells were osteogenically induced. ALP staining showed that the N-hPDLSCs displayed the deepest color. Alizarin red staining indicated that the A-hPDLSCs group had less calcified nodules than the N-hPDLSCs group. The real time PCR results suggested that the expression of relative osteogenic genes in A-hPDLSCs was quite low. Statistically significant differences in differentiation were found between groups (P < 0.05). The Western blot result was similar to that of real time PCR. Classical Wnt signaling pathway-related factor β-catenin was higher in A-hPDLSCs than in N-hPDLSCs. By contrast, DKK-1, which is an inhibitor in the Wnt pathway, had a significantly lower expression rate in A-hPDLSCs than in N-hPDLSCs. The Western blot result also showed that β-catenin expression in the nucleoprotein in A-hPDLSCs was notably higher than in N-hPDLSCs.
AGEs can inhibit hPDLSCs osteogenic differentiation. AGEs induce changes in the normal periodontal ligament stem cells classical Wnt pathway. Canonical Wnt pathway is reactivated because of AGEs stimulation.
探讨晚期糖基化终末产物(AGEs)对人牙周膜干细胞(hPDLSCs)成骨分化的影响,并确定糖基化过程中Wnt信号通路的变化。
主要采用体外组织块培养法。通过有限稀释克隆培养在体外获得hPDLSCs。将研究对象分为两组:健康组(N-hPDLSCs)和AGEs刺激组(A-hPDLSCs)。对实验组进行成骨细胞矿化诱导。进行以下操作:茜素红染色;碱性磷酸酶(ALP)染色;实时聚合酶链反应(实时PCR)检测成骨基因及Wnt经典通路相关因子DKK-1和β-连环蛋白;蛋白质免疫印迹分析。分析骨蛋白与β-连环蛋白的核表达相关性。
对细胞进行成骨诱导。ALP染色显示N-hPDLSCs颜色最深。茜素红染色表明,A-hPDLSCs组钙化结节少于N-hPDLSCs组。实时PCR结果提示,A-hPDLSCs中相对成骨基因的表达相当低。两组间分化存在统计学显著差异(P < 0.05)。蛋白质免疫印迹结果与实时PCR结果相似。经典Wnt信号通路相关因子β-连环蛋白在A-hPDLSCs中高于N-hPDLSCs。相比之下,作为Wnt通路抑制剂的DKK-1在A-hPDLSCs中的表达率显著低于N-hPDLSCs。蛋白质免疫印迹结果还显示,A-hPDLSCs中核蛋白内β-连环蛋白的表达明显高于N-hPDLSCs。
AGEs可抑制hPDLSCs的成骨分化。AGEs诱导正常牙周膜干细胞经典Wnt通路发生变化。由于AGEs刺激,经典Wnt通路被重新激活。