PHD2 shRNA修饰的骨髓间充质干细胞在炎症条件下促进牙周骨质修复

Bin Yan Luo, Shu Yu Cheng, Wen Zheng Liao, Bao Chun Tan, Di Cui, Min Wang, Jun Qian, Chang Xing Chen, Fu Hua Yan
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引用次数: 0

摘要

目的研究骨髓间充质干细胞(BMMSCs)是否在炎症条件下通过含羟化酶结构域蛋白2(PHD2)/缺氧诱导因子-1(HIF-1)信号通路调节牙周骨质修复:方法:在体外卟啉菌牙龈脂多糖(Pg-LPS)刺激的炎症微环境中,探讨了 PHD2 shRNA 修饰的 BMMSCs 的成骨分化及其可能机制。通过实验性牙周炎评估了 PHD2 基因修饰的 BMMSCs 对牙周骨质流失的影响:结果:Pg-LPS 的刺激极大地损害了 BMMSCs 的成骨分化,而 PHD2 的沉默则显著增强了 BMMSCs 的成骨作用。更重要的是,Pg-LPS刺激下血管内皮生长因子(VEGF)水平升高,这被证实与成骨增强有关。在实验性牙周炎中,PHD2修饰的BMMSCs移植可提高牙周组织的成骨参数和血管内皮生长因子的表达:本研究强调,PHD2 基因沉默可通过挽救种子细胞的功能障碍来对抗炎症性骨质流失,是一种可行的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PHD2 shRNA-Modified Bone Marrow Mesenchymal Stem Cells Facilitate Periodontal Bone Repair in Response to Inflammatory Condition.

Objective: To investigate whether bone marrow mesenchymal stem cells (BMMSCs) modulate periodontal bone repair through the hydroxylase domain-containing protein 2 (PHD2)/hypoxia- inducible factor-1 (HIF-1) signalling pathway in response to inflammatory conditions.

Methods: Osteogenic differentiation of PHD2 shRNA-modified BMMSCs and the possible mechanism were explored in an inflammatory microenvironment stimulated by porphyromonas gingivalis lipopolysaccharide (Pg-LPS) in vitro. The effect of PHD2 gene-modified BMMSCs on periodontal bone loss was evaluated with experimental periodontitis.

Results: Pg-LPS stimulation greatly impaired the osteogenic differentiation of BMMSCs, whereas the silence of PHD2 significantly enhanced the osteogenesis of BMMSCs. More importantly, increased level of vascular endothelial growth factor (VEGF) was detected under Pg-LPS stimulation, which was verified to be associated with the augmented osteogenesis. In experimental periodontitis, PHD2-modified BMMSCs transplantation elevated osteogenic parameters and the expression of VEGF in periodontal tissue.

Conclusion: This study highlighted that PHD2 gene silencing could be a feasible approach to combat inflammatory bone loss by rescuing the dysfunction of seed cells.

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