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首页> 外文期刊>American Journal of Translational Research >Loss of Wnt4 expression inhibits the odontogenic potential of dental pulp stem cells through JNK signaling in pulpitis
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Loss of Wnt4 expression inhibits the odontogenic potential of dental pulp stem cells through JNK signaling in pulpitis

机译:Wnt4表达的丧失通过牙髓炎中的JNK信号传导抑制牙髓干细胞的牙源性潜力

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Dental pulp stem cell (DPSC)-based odontogenic regeneration in inflammatory conditions is important in the process of pulpitis. DPSCs have been reported to lose potential for odontogenic regeneration in inflammatory conditions. This study aims to determine the mechanism of impaired odontogenic differentiation of DPSCs in an inflammatory microenvironment. We regulated Wnt4 expression using recombinant lentiviral Wnt4 and Wnt4 siRNA. Alkaline phosphatase (ALP) and Alizarin red S (ARS) staining as well as Real-Time PCR were performed to evaluate the osteogenic differentiation potential of DPSCs with either upregulated or downregulated Wnt4. Furthermore, SP600125 was used to inhibit the potential downstream factor JNK1, and the osteogenic differentiation ability of DPSCs was evaluated. As shown, Wnt4 was downregulated in DPSCs under inflammatory conditions. Inhibition of Wnt4 expression in DPSCs negatively regulated odontogenic differentiation. Overexpression of Wnt4 in LPS-treated DPSCs promoted odontogenic differentiation. In addition, JNK1 was responsible for Wnt4-mediated odontogenic differentiation of DPSCs. Taken together, Wnt4 may function by affecting JNK signaling pathways in the process of impaired odontogenic regeneration by DPSCs under inflammatory conditions.
机译:牙髓炎过程中,炎症条件下基于牙髓干细胞(DPSC)的牙源性再生很重要。据报道,DPSC在炎性条件下丧失牙源性再生的潜力。这项研究旨在确定在炎性微环境中DPSC的牙源性分化受损的机制。我们使用重组慢病毒Wnt4和Wnt4 siRNA调节Wnt4的表达。进行碱性磷酸酶(ALP)和茜素红S(ARS)染色以及实时PCR来评估Wnt4上调或下调的DPSCs的成骨分化潜能。此外,使用SP600125抑制潜在的下游因子JNK1,并评估了DPSC的成骨分化能力。如图所示,在炎性条件下,DPSC中的Wnt4被下调。在DPSC中Wnt4表达的抑制负调控牙源性分化。在LPS处理的DPSC中Wnt4的过表达促进了牙源性分化。此外,JNK1负责Wnt4介导的DPSC牙源性分化。两者合计,Wnt4可能通过影响炎症条件下DPSC的成牙本质再生受损过程中的JNK信号传导途径而起作用。

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