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Increased Osteogenic Differentiation of Periodontal Ligament Stem Cells on Polydopamine Film Occurs via Activation of Integrin and PI3K Signaling Pathways

机译:通过整合素和PI3K信号通路的激活增加聚多巴胺膜上牙周膜干细胞成骨分化的增加。

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Background/Aims: Mussel-inspired polydopamine (PDA) is known to be an effective bioadhesive and bioactive material for controlling stem cell fate, which is important in stem cell-based regenerative medicine; however, the effect of PDA on osteogenic differentiation of periodontal ligament stem cells (PDLSCs) is not fully understood. In this study, we investigated the osteoinductive effect of PDA on PDLSCs and examined how this phenomenon is encouraged. Methods: Osteogenic induction of PDLSCs was established by culturing cells on PDA film or on an uncoated polystyrene surface as a control. Osteogenic differentiation of PDLSCs was assessed by measurement of intracellular calcium levels and alkaline phosphatase (ALP) activity as well as by evaluation of protein expression of osteocalcin (OCN), osterix (OSX), and runt-related transcription factor 2 (RUNX2). Results: The PDLSCs cultured on PDA film showed higher osteogenic activity than those on the control surface. Moreover, PDLSCs on PDA film expressed increased levels of the integrin adhesion receptors integrin α5 and β1 compared to control cells. Expression of one isoform of the intracellular signaling protein phosphatidylinositol-3-kinase (PI3K), p110γ, was increased in PDLSCs on PDA film in a PDA dose-dependent manner. This signaling protein was found to interact with integrin β1, demonstrating integrin-linked PI3K activation in response to PDA. Finally, the blockage of PI3K reduced the PDA-induced osteogenic activity of PDLSCs. Conclusion: our findings suggest that the bioadhesive PDA stimulates osteogenic differentiation of PDLSCs via activation of the integrin α5/β1 and PI3K signaling pathways.
机译:背景/目的:受到贻贝启发的聚多巴胺(PDA)是控制干细胞命运的有效生物粘附和生物活性材料,在基于干细胞的再生医学中很重要。但是,PDA对牙周膜干细胞(PDLSCs)成骨分化的作用尚不完全清楚。在这项研究中,我们调查了PDA对PDLSCs的骨诱导作用,并研究了如何鼓励这种现象。方法:通过在PDA膜或未涂覆的聚苯乙烯表面上培养细胞作为对照,建立PDLSC的成骨诱导作用。通过测量细胞内钙水平和碱性磷酸酶(ALP)活性以及评估骨钙蛋白(OCN),osterix(OSX)和矮子相关转录因子2(RUNX2)的蛋白质表达来评估PDLSC的成骨分化。结果:在PDA膜上培养的PDLSCs的成骨活性高于对照表面。此外,与对照细胞相比,PDA膜上的PDLSCs表达的整合素粘附受体整合素α5和β1水平升高。细胞内信号蛋白磷脂酰肌醇-3-激酶(PI3K)的一种同工型p110γ的表达以PDA剂量依赖性方式在PDA膜上的PDLSC中增加。发现该信号蛋白与整联蛋白β1相互作用,表明整联蛋白连接的PI3K激活对PDA的响应。最后,PI3K的阻滞降低了PDA诱导的PDLSCs的成骨活性。结论:我们的发现表明,生物粘附性PDA通过激活整联蛋白α5/β1和PI3K信号通路来刺激PDLSC的成骨分化。

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