Department of Stomatology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Department of Medical Cosmetology, Suining Central Hospital, Suining, China.
J Biomed Mater Res B Appl Biomater. 2022 Apr;110(4):755-767. doi: 10.1002/jbm.b.34954. Epub 2021 Oct 12.
Human-treated dentin matrix (hTDM) is a biomaterial scaffold, which can induce implant cells to differentiate into odontoblasts and then form neo-dentin. However, hTDM with long storage or prepared by high-speed handpiece would not to form neo-dentin. In this research, we developed two fresh hTDM with different grinding speeds, which were low-speed hTDM (LTDM) with maximum speed of 500 rpm and high-speed hTDM (HTDM) with a speed of 3,80,000 rpm. Here, we aim to understand whether there were induced regeneration capacity differences between LTDM and HTDM. Scanning electron microscope showed that DFCs grew well on both materials, but the morphology of DFCs and the extracellular matrix was different. Especially, the secreted extracellular matrixes on the inner surface of LTDM were regular morphology and ordered arrangement around the dentin tubules. The transcription-quantitative polymerase chain reaction (qRT-PCR), western blot and immunofluorescence assay showed that the dentin markers DSPP and DMP-1 were about 2× greater in DFCs induced by LTDM than by HTDM, and osteogenic marker BSP was about 2× greater in DFCs induced by HTDM than by LTDM. Histological examinations of the harvested grafts observed the formation of neo-tissue were different, and there were neo-dentin formed on the inner surface of LTDM and neo-cementum formed on the outer surface of HTDM. In summary, it found that the induction abilities of LTDM and HTDM are different, and the dentin matrix is directional. This study lays a necessary foundation for searching the key factors of dentin regeneration in future.
人处理牙本质基质(hTDM)是一种生物材料支架,可诱导种植细胞分化为成牙本质细胞,然后形成新生牙本质。然而,储存时间长或用高速手机制备的 hTDM 不会形成新生牙本质。在这项研究中,我们开发了两种不同研磨速度的新鲜 hTDM,低速 hTDM(LTDM)的最大速度为 500rpm,高速 hTDM(HTDM)的速度为 380000rpm。在这里,我们旨在了解 LTDM 和 HTDM 之间是否存在诱导再生能力的差异。扫描电子显微镜显示,DFCs 在两种材料上生长良好,但 DFCs 的形态和细胞外基质不同。特别是,LTDM 内表面分泌的细胞外基质形态规则,围绕牙本质小管有序排列。转录定量聚合酶链反应(qRT-PCR)、western blot 和免疫荧光分析显示,LTDM 诱导的 DFCs 中牙本质标志物 DSPP 和 DMP-1 的转录水平约为 HTDM 诱导的 2 倍,而 HTDM 诱导的 DFCs 中骨形成标志物 BSP 的转录水平约为 LTDM 诱导的 2 倍。对收获移植物的组织学检查观察到形成的新生组织不同,LTDM 内表面形成新生牙本质,HTDM 外表面形成新生类骨质。综上所述,发现 LTDM 和 HTDM 的诱导能力不同,牙本质基质具有方向性。本研究为今后寻找牙本质再生的关键因素奠定了必要的基础。