Semaphorin 3A Confers Protection against Oxidative Stress-induced Damage in Periodontal Ligament Stem Cells through the Activation of the Wnt/β-catenin Signaling Pathway.

Haipeng He, Xueshun Yuan, Yanyan Chen, Tianyong Hu, Baohui Cheng, Ruitian Du, Jiamin Huang, Xiaorui Geng, Hongwen Li, Senqing Liu, Zhiqiang Liu
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Abstract

Objectives: The osteogenic potential of periodontal ligament stem cells (PDLSCs) is crucial for periodontal tissue regeneration. Prolonged and excessive oxidative stress (OS) impairs the osteogenic function of PDLSCs. Recently, Semaphorin 3A (Sema3A) has been reported to have multiple roles in bone protection. This study aimed to investigate the protective effect of Sema3A on the osteogenic differentiation of PDLSCs under OS conditions induced by hydrogen peroxide (H2O2).

Methods: PDLSCs were subjected to H2O2 treatment to induce OS. The OS indices in PDLSCs were evaluated by analyzing levels of reactive oxygen species (ROS), cell viability, and expression of antioxidant factors using relevant assay kits. A small molecule inhibitor, XAV-939, was employed to block the Wnt/β-catenin pathway. Osteogenic differentiation was assessed using alkaline phosphatase (ALP) activity staining and Alizarin Red S (ARS) staining for mineralized nodules. Expression levels of osteogenic gene markers and β-catenin were determined via real-time quantitative polymerase chain reaction (RT-qPCR) or western blot (WB) analysis.

Results: The stimulation of H2O2 induced OS in PDLSCs, resulting in a downregulation of Sema3A expression and a decrease in osteogenic markers, including ALP activity, mineralized nodule formation, and the expression of osteogenic genes (RUNX2 and ALP). However, the application of recombinant human Sema3A (rhSema3A) counteracted H2O2-induced OS and restored these osteogenic markers in PDLSCs under OS induced by H2O2. Mechanistic studies revealed that these effects were associated with an upregulation of β-catenin levels. Moreover, inhibiting β-- catenin expression compromised the protective effect of Sema3A on osteogenesis in PDLSCs under OS.

Conclusion: Sema3A exerts a protective effect against H2O2-induced OS and activates the Wnt/β-- catenin pathway to restore osteogenic differentiation impaired by OS in PDLSCs.

Semaphorin 3A通过激活Wnt/β-catenin信号通路对氧化应激诱导的牙周韧带干细胞损伤的保护作用
目的:牙周韧带干细胞(PDLSCs)的成骨潜能对牙周组织再生至关重要。长期和过度的氧化应激(OS)会损害PDLSCs的成骨功能。最近,有报道称信号蛋白3A (Sema3A)在骨保护中具有多种作用。本研究旨在探讨Sema3A对过氧化氢(H2O2)诱导的OS条件下PDLSCs成骨分化的保护作用。方法:对PDLSCs进行H2O2处理诱导OS。采用相关检测试剂盒,通过分析活性氧(ROS)水平、细胞活力和抗氧化因子表达来评估PDLSCs的OS指标。一种小分子抑制剂XAV-939被用来阻断Wnt/β-catenin通路。矿化结节采用碱性磷酸酶(ALP)活性染色和茜素红S (ARS)染色评估成骨分化。通过实时定量聚合酶链反应(RT-qPCR)或western blot (WB)检测成骨基因标志物和β-catenin的表达水平。结果:H2O2刺激诱导PDLSCs发生OS,导致Sema3A表达下调,成骨标志物(包括ALP活性、矿化结节形成、成骨基因RUNX2和ALP)表达降低。然而,重组人Sema3A (rhSema3A)的应用抵消了H2O2诱导的OS,并在H2O2诱导的OS下恢复了PDLSCs中这些成骨标志物。机制研究表明,这些作用与β-连环蛋白水平上调有关。此外,抑制β- catenin表达削弱了Sema3A对OS下PDLSCs成骨的保护作用。结论:Sema3A对h2o2诱导的OS具有保护作用,激活Wnt/β- catenin通路,恢复OS损伤的PDLSCs成骨分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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