1 Department of Oral Biology, University of Illinois at Chicago, Chicago, IL, USA.
2 Department of Oral Biology, Aix Marseille Université, Marseille, France.
J Dent Res. 2019 May;98(5):597-604. doi: 10.1177/0022034518820461. Epub 2019 Jan 31.
The presence of stem cells within the dental-pulp tissue as well as their differentiation into a new generation of functional odontoblast-like cells constitutes an important step of the dentin-pulp regeneration. Recent investigations demonstrated that the complement system activation participates in 2 critical steps of dentin-pulp regeneration: pulp progenitor's recruitment and pulp nerve sprouting. Surprisingly, its implication in odontoblastic differentiation has not been addressed yet. Since the complement receptor C5a receptor-like 2 (C5L2) is expressed by different stem cells, the aim of this study is to investigate if the dental pulp stem cells express C5L2 and if this receptor participates in odontoblastic differentiation. Immunohistochemistry performed on human third molar pulp sections showed a perivascular co-localization of the mesenchymal stem cell markers STRO1 and C5L2. In vitro immunofluorescent staining confirmed that hDPSCs express C5L2. Furthermore, we determined by real-time polymerase chain reaction that the expression of C5L2 is highly modulated in human dental pulp stem cells (hDPSCs) undergoing odontoblastic differentiation. Moreover, we showed that this odontogenesis-regulated expression of C5L2 is specifically potentiated by the proinflammatory cytokine TNFα. Using a C5L2-siRNA silencing strategy, we provide direct evidence that C5L2 constitutes a negative regulator of the dentinogenic marker DMP1 (dentin matrix protein 1) expression by hDPSCs. Our findings suggest a direct correlation between the odontoblastic differentiation and the level of C5L2 expression in hDPSCs and identify C5L2 as a negative regulator of DMP1 expression by hDPSCs during the odontoblastic differentiation and inflammation processes. This work is the first to demonstrate the involvement of C5L2 in the biological function of stem cells, provides an important knowledge in understanding odontoblastic differentiation of dental pulp stem cells, and may be useful in future dentin-pulp engineering strategies.
牙髓组织中存在干细胞,并且这些干细胞分化为新一代具有功能性成牙本质细胞样的细胞,这是牙本质-牙髓再生的重要步骤。最近的研究表明,补体系统的激活参与了牙本质-牙髓再生的两个关键步骤:牙髓祖细胞的募集和牙髓神经的发芽。令人惊讶的是,其在成牙本质细胞分化中的作用尚未得到解决。由于补体受体 C5a 受体样 2(C5L2)被不同的干细胞表达,因此本研究旨在探讨牙髓干细胞是否表达 C5L2,以及该受体是否参与成牙本质细胞分化。对人第三磨牙牙髓切片进行免疫组织化学染色显示,间充质干细胞标志物 STRO1 和 C5L2 存在血管周围共定位。体外免疫荧光染色证实 hDPSCs 表达 C5L2。此外,我们通过实时聚合酶链反应确定 C5L2 在经历成牙本质细胞分化的人牙髓干细胞(hDPSCs)中的表达高度调节。此外,我们表明,这种 C5L2 的牙发生调节表达是由促炎细胞因子 TNFα 特异性增强的。使用 C5L2-siRNA 沉默策略,我们提供了直接证据表明,C5L2 是 hDPSCs 中牙本质生成标志物 DMP1(牙本质基质蛋白 1)表达的负调节剂。我们的研究结果表明,C5L2 的表达水平与 hDPSCs 的成牙本质细胞分化之间存在直接相关性,并确定 C5L2 是 hDPSCs 成牙本质分化和炎症过程中 DMP1 表达的负调节剂。这项工作首次证明了 C5L2 参与了干细胞的生物学功能,为理解牙髓干细胞的成牙本质细胞分化提供了重要的知识,并可能对未来的牙本质-牙髓工程策略有用。