Department of Oral and Maxillofacial Surgery, University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, 93053 Regensburg, Germany.
Int J Mol Sci. 2022 May 25;23(11):5945. doi: 10.3390/ijms23115945.
Human dental follicle cells (DFCs) as periodontal progenitor cells are used for studies and research in regenerative medicine and not only in dentistry. Even if innovative regenerative therapies in medicine are often considered the main research area for dental stem cells, these cells are also very useful in basic research and here, for example, for the elucidation of molecular processes in the differentiation into mineralizing cells. This article summarizes the molecular mechanisms driving osteogenic differentiation of DFCs. The positive feedback loop of bone morphogenetic protein (BMP) 2 and homeobox protein DLX3 and a signaling pathway associated with protein kinase B (AKT) and protein kinase C (PKC) are presented and further insights related to other signaling pathways such as the WNT signaling pathway are explained. Subsequently, some works are presented that have investigated epigenetic modifications and non-coding ncRNAs and their connection with the osteogenic differentiation of DFCs. In addition, studies are presented that have shown the influence of extracellular matrix molecules or fundamental biological processes such as cellular senescence on osteogenic differentiation. The putative role of factors associated with inflammatory processes, such as interleukin 8, in osteogenic differentiation is also briefly discussed. This article summarizes the most important insights into the mechanisms of osteogenic differentiation in DFCs and is intended to be a small help in the direction of new research projects in this area.
人牙龈滤泡细胞(DFC)作为牙周前体细胞,用于再生医学的研究和开发,不仅在牙科领域。尽管创新性的再生疗法在医学中常被认为是牙科干细胞的主要研究领域,但这些细胞在基础研究中也非常有用,例如,用于阐明向矿化细胞分化的分子过程。本文总结了驱动 DFC 成骨分化的分子机制。介绍了骨形态发生蛋白(BMP)2 和同源盒蛋白 DLX3 的正反馈环,以及与蛋白激酶 B(AKT)和蛋白激酶 C(PKC)相关的信号通路,并进一步解释了与 WNT 信号通路等其他信号通路相关的见解。随后,介绍了一些研究调查了表观遗传修饰和非编码 ncRNA 及其与 DFC 成骨分化的关系。此外,还介绍了一些研究表明细胞外基质分子或细胞衰老等基本生物学过程对成骨分化的影响。也简要讨论了与炎症过程相关的因素(如白细胞介素 8)在成骨分化中的潜在作用。本文总结了 DFC 成骨分化机制的最重要见解,旨在为该领域的新研究项目提供一点帮助。
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