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JNK MAPK is involved in BMP-2-induced odontoblastic differentiation of human dental pulp cells

机译:JNK MAPK参与BMP-2诱导的人类牙髓细胞的牙本质成骨分化

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Bone morphogenetic protein-2 (BMP-2) is a multi-functional growth factor belonging to the transforming growth factor β superfamily that has a broad range of activities that affect many different cell types. BMP-2 induces odontoblastic differentiation of human dental pulp cells (DPCs), but the underlying mechanism remains unclear. In this study, we investigated the potential role of the JNK mitogen-activated protein kinases (MAPK) pathway in BMP-2-induced odontoblastic differentiation of DPCs. The levels of phosphorylated and unphosphorylated JNK MAPK were quantified by Western blot analysis following treatment with BMP-2 and the JNK inhibitor SP600125. The role of JNK MAPK in the BMP-2-induced odontoblastic differentiation of DPCs was determined by measuring alkaline phosphatase (ALP) activity and by examining the expression of odontoblastic markers using quantitative real-time polymerase chain reaction analysis. The effect of JNK MAPK silencing on odontoblastic differentiation was also investigated. BMP-2 upregulated the phosphorylation of JNK in DPCs in a dose- and time-dependent manner. Early markers of odontoblastic differentiation, including ALP activity, osteopontin and dentin matrix protein-1, were not inhibited by the JNK inhibitor. However, the JNK inhibitor, SP600125, significantly inhibited late-stage differentiation of odontoblasts, including the gene expression of osteocalcin, dentin sialophosphoprotein and bone sialoprotein, and also reduced the formation of mineralized nodules in BMP-2-treated DPCs. Consistent with this observation, silencing of JNK MAPK also decreased late-stage odontoblastic differentiation. Taken together, these findings suggest that JNK activity is required for late-stage odontoblastic differentiation induced by BMP-2.
机译:骨形态发生蛋白2(BMP-2)是属于转化生长因子β超家族的多功能生长因子,具有影响许多不同细胞类型的广泛活性。 BMP-2诱导人牙髓细胞(DPC)的牙本质成骨细胞分化,但其潜在机制仍不清楚。在这项研究中,我们调查了JNK丝裂原激活的蛋白激酶(MAPK)途径在BMP-2诱导DPC牙本质成骨分化中的潜在作用。在用BMP-2和JNK抑制剂SP600125处理后,通过Western blot分析定量磷酸化和未磷酸化的JNK MAPK的水平。通过测量碱性磷酸酶(ALP)活性并使用定量实时聚合酶链反应分析检查牙本质母标记物的表达,确定了JNK MAPK在BMP-2诱导的牙髓母细胞分化中的作用。还研究了JNK MAPK沉默对成牙本质细胞分化的影响。 BMP-2以剂量和时间依赖性方式上调DPC中JNK的磷酸化。 JNK抑制剂不会抑制牙本质成骨细胞分化的早期标志物,包括ALP活性,骨桥蛋白和牙本质基质蛋白1。但是,JNK抑制剂SP600125显着抑制成牙本质细胞的后期分化,包括骨钙素,牙本质唾液磷蛋白和骨唾液蛋白的基因表达,并且还减少了BMP-2处理的DPC中矿化结节的形成。与该观察结果一致,JNK MAPK沉默也降低了晚期牙成骨细胞分化。综上所述,这些发现表明,JMP活性是BMP-2诱导的晚期齿突细胞分化所必需的。

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