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牙髓干细胞在第三期牙本质形成过程中被巨噬细胞调控。

Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis.

机构信息

Centre for Craniofacial and Regenerative Biology, Faculty of Dentistry, Oral and Craniofacial Sciences, Kings College London, Floor 27, Guy's Tower, Guy's Hospital, London, SE1 9RT, UK.

Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral and Craniofacial Sciences, Kings College London, London, UK.

出版信息

Sci Rep. 2020 Nov 19;10(1):20216. doi: 10.1038/s41598-020-77161-4.

Abstract

The interaction between immune cells and stem cells is important during tissue repair. Macrophages have been described as being crucial for limb regeneration and in certain circumstances have been shown to affect stem cell differentiation in vivo. Dentine is susceptible to damage as a result of caries, pulp infection and inflammation all of which are major problems in tooth restoration. Characterising the interplay between immune cells and stem cells is crucial to understand how to improve natural repair mechanisms. In this study, we used an in vivo damage model, associated with a macrophage and neutrophil depletion model to investigate the role of immune cells in reparative dentine formation. In addition, we investigated the effect of elevating the Wnt/β-catenin pathway to understand how this might regulate macrophages and impact upon Wnt receiving pulp stem cells during repair. Our results show that macrophages are required for dental pulp stem cell activation and appropriate reparative dentine formation. In addition, pharmacological stimulation of the Wnt/β-catenin pathway via GSK-3β inhibitor small molecules polarises macrophages to an anti-inflammatory state faster than inert calcium silicate-based materials thereby accelerating stem cell activation and repair. Wnt/β-catenin signalling thus has a dual role in promoting reparative dentine formation by activating pulp stem cells and promoting an anti-inflammatory macrophage response.

摘要

免疫细胞和干细胞之间的相互作用对于组织修复很重要。巨噬细胞在肢体再生中起着至关重要的作用,在某些情况下,已被证明会影响体内干细胞的分化。牙本质很容易因龋齿、牙髓感染和炎症而受损,所有这些都是牙齿修复的主要问题。描述免疫细胞和干细胞之间的相互作用对于了解如何改善自然修复机制至关重要。在这项研究中,我们使用了一种体内损伤模型,结合巨噬细胞和中性粒细胞耗竭模型,研究了免疫细胞在修复性牙本质形成中的作用。此外,我们还研究了升高 Wnt/β-catenin 途径的作用,以了解这如何调节巨噬细胞,并在修复过程中对接收 Wnt 的牙髓干细胞产生影响。我们的结果表明,巨噬细胞是牙髓干细胞激活和适当修复性牙本质形成所必需的。此外,通过 GSK-3β 抑制剂小分子对 Wnt/β-catenin 途径进行药理学刺激,比惰性硅酸钙基材料更快地将巨噬细胞极化到抗炎状态,从而加速干细胞的激活和修复。因此,Wnt/β-catenin 信号通路通过激活牙髓干细胞和促进抗炎性巨噬细胞反应,在促进修复性牙本质形成方面具有双重作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b3f/7678850/73137947fa97/41598_2020_77161_Fig1_HTML.jpg

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