Department of Oral Health Sciences, School of Dentistry, University of Washington, Seattle, WA, USA.
Center for Cardiovascular Biology, University of Washington, Seattle, WA, USA.
J Dent Res. 2024 Sep;103(10):1008-1016. doi: 10.1177/00220345241264792. Epub 2024 Aug 26.
In vitro models are invaluable tools for deconstructing the biological complexity of the periodontal ligament (PDL). Model systems that closely reproduce the 3-dimensional (3D) configuration of cell-cell and cell-matrix interactions in native tissue can deliver physiologically relevant insights. However, 3D models of the PDL that incorporate mechanical loading are currently lacking. Hence, we developed a model where periodontal tissue constructs (PTCs) are made by casting PDL cells in a collagen gel suspended between a pair of slender, silicone posts for magnetic tensile loading. Specifically, one of the posts was rigid and the other was flexible with a magnet embedded in its tip so that PTCs could be subjected to tensile loading with an external magnet. Additionally, the deflection of the flexible post could be used to measure the contractile force of PDL cells in the PTCs. Prior to tensile loading, second harmonics generation analysis of collagen fibers in PTCs revealed that incorporation of PDL cells resulted in collagen remodeling. Biomechanical testing of PTCs by tensile loading revealed an elastic response at 4 h, permanent deformation by 1 d, and creep elongation by 1 wk. Subsequently, contractile forces of PDL cells were substantially lower for PTCs under tensile loading. Immunofluorescence analysis revealed that tensile loading caused PDL cells to increase in number, express higher levels of F-actin and α-smooth muscle actin, and become aligned to the tensile axis. Second harmonics generation analysis indicated that collagen fibers in PTCs progressively remodeled over time with tensile loading. Gene expression analysis also confirmed tension-mediated upregulation of the F-actin/Rho pathway and osteogenic genes. Our model is novel in demonstrating the mechanobiological behavior that results in cell-mediated remodeling of the PDL tissue in a 3D context. Hence, it can be a valuable tool to develop therapeutics for periodontitis, periodontal regeneration, and orthodontics.
在体外模型中,可以对牙周韧带(PDL)的生物学复杂性进行解构,这些模型非常有价值。能够重现天然组织中细胞-细胞和细胞-基质相互作用的 3 维(3D)结构的模型系统,可以提供具有生理相关性的见解。然而,目前缺乏可纳入机械加载的牙周韧带 3D 模型。因此,我们开发了一种模型,其中牙周组织构建体(PTCs)是通过将 PDL 细胞浇注在悬浮于一对细长的硅树脂柱之间的胶原凝胶中来制作的,这对硅树脂柱用于磁拉伸加载。具体来说,其中一根柱子是刚性的,另一根柱子是柔性的,其尖端嵌入了一块磁铁,这样 PTC 就可以用外部磁铁进行拉伸加载。此外,柔性柱的挠度可用于测量 PTC 中 PDL 细胞的收缩力。在拉伸加载之前,通过对 PTC 中的胶原纤维进行二次谐波产生分析,发现 PDL 细胞的掺入导致了胶原重塑。通过拉伸加载对 PTC 进行生物力学测试,结果显示 4 小时时呈现弹性响应,1 天时出现永久变形,1 周时出现蠕变伸长。随后,在拉伸加载下,PTC 中的 PDL 细胞收缩力明显降低。免疫荧光分析显示,拉伸加载会导致 PDL 细胞数量增加,表达更高水平的 F-肌动蛋白和α-平滑肌肌动蛋白,并沿拉伸轴对齐。二次谐波产生分析表明,随着时间的推移,胶原纤维在 PTC 中逐渐重塑,并且在拉伸加载下。基因表达分析也证实了张力介导的 F-肌动蛋白/ Rho 通路和成骨基因的上调。我们的模型的新颖之处在于,它展示了导致牙周组织在 3D 环境中发生细胞介导重塑的力学生物学行为。因此,它可以成为开发治疗牙周炎、牙周再生和正畸的有价值的工具。