Department of Orthodontics, Dental Clinic, University of Aachen, 52074 Aachen, Germany.
Department of Orthodontics, Dental Clinic, University of Aachen, 52074 Aachen, Germany; Helmholtz Institute for Biomedical Engineering, Bionterface Group, RWTH Aachen University, 52056 Aachen, Germany; Institute of Pathology, RWTH Aachen University Hospital, 52074, Germany.
Ann Anat. 2023 Aug;249:152102. doi: 10.1016/j.aanat.2023.152102. Epub 2023 May 6.
One of the major components in cementum extracellular matrix is bone sialoprotein (BSP). BSP knockout (Ibsp) mice were reported to have a nonfunctional hypo-mineralized cementum, as well as detachment and disorganization of the periodontal ligament tissue. However, studies investigating the influence of Ibsp in cementoblasts are missing yet. This study investigates the influences of Bsp in three cementoblasts cell lines (OCCM.30-WT,Ibsp, and Ibsp). The mRNA expression of cementoblast and osteoclast markers (Col1a1, Alpl, Ocn, Runx2, Ctsk, Rankl and Opg) and the cell morphology were compared. Additionally, a functional monocyte adhesion assay was performed. To understand the influence of external stimuli, the effect of Ibsp was investigated under static compressive force, mimicking the compression side of orthodontic tooth movement. Cementoblasts with genotype Ibsp and Ibsp showed slight differences in cell morphology compared to OCCM.30-WT, as well as different gene expression. Under compressive force, the Ibsp cell lines presented expression pattern markers similar to the OCCM.30-WT cell line. However, Cathepsin K was strongly upregulated in Ibsp cementoblasts under compressive force. This study provides insight into the role of BSP in cementoblasts and explores the influence of BSP on periodontal ligament tissues. BSP markers in cementoblasts seem to be involved in the regulation of cementum organization as an important factor for a functional periodontium. In summary, our findings provide a basis for investigations regarding molecular biology interactions of BSP in cementoblasts, and a supporting input for understanding the periodontal and cellular cementum remodeling.
牙骨质细胞外基质的主要成分之一是骨涎蛋白 (BSP)。有报道称,BSP 基因敲除 (Ibsp) 小鼠的牙骨质出现功能性矿化不全,牙周韧带组织分离和结构紊乱。然而,目前尚缺乏关于 Ibsp 对成牙骨质细胞影响的研究。本研究旨在探讨 BSP 在三种成牙骨质细胞系 (OCCM.30-WT、Ibsp 和 Ibsp) 中的作用。比较了成牙骨质细胞和破骨细胞标志物 (Col1a1、Alpl、Ocn、Runx2、Ctsk、Rankl 和 Opg) 的 mRNA 表达和细胞形态。此外,还进行了功能性单核细胞黏附试验。为了了解外部刺激的影响,在模拟正畸牙移动受压侧的静态压缩力下研究了 Ibsp 的作用。与 OCCM.30-WT 相比,Ibsp 和 Ibsp 基因型的成牙骨质细胞的细胞形态略有不同,基因表达也不同。在压力下,Ibsp 细胞系呈现出与 OCCM.30-WT 细胞系相似的表达模式标记物。然而,在压力下,Ibsp 成牙骨质细胞中的组织蛋白酶 K 强烈上调。本研究深入探讨了 BSP 在成牙骨质细胞中的作用,并研究了 BSP 对牙周韧带组织的影响。成牙骨质细胞中的 BSP 标志物似乎参与了牙骨质组织的调节,是功能性牙周组织的重要因素。综上所述,我们的研究结果为探讨 BSP 在成牙骨质细胞中的分子生物学相互作用提供了依据,并为理解牙周和细胞性牙骨质重塑提供了支持。