Suttorp Christiaan M, Xie Rui, Lundvig Ditte M S, Kuijpers-Jagtman Anne Marie, Uijttenboogaart Jasper Tom, Van Rheden René, Maltha Jaap C, Wagener Frank A D T G
Department of Orthodontics and Craniofacial Biology, Radboud university medical centre, Radboud Institute for Molecular Life Sciences Nijmegen, Netherlands.
Front Physiol. 2016 Jul 19;7:283. doi: 10.3389/fphys.2016.00283. eCollection 2016.
Orthodontic forces disturb the microenvironment of the periodontal ligament (PDL), and induce craniofacial bone remodeling which is necessary for tooth movement. Unfortunately, orthodontic tooth movement is often hampered by ischemic injury and cell death within the PDL (hyalinization) and root resorption. Large inter-individual differences in hyalinization and root resorption have been observed, and may be explained by differential protection against hyalinization. Heme oxygenase-1 (HO-1) forms an important protective mechanism by breaking down heme into the strong anti-oxidants biliverdin/bilirubin and the signaling molecule carbon monoxide. These versatile HO-1 products protect against ischemic and inflammatory injury. We postulate that orthodontic forces induce HO-1 expression in the PDL during experimental tooth movement. Twenty-five 6-week-old male Wistar rats were used in this study. The upper three molars at one side were moved mesially using a Nickel-Titanium coil spring, providing a continuous orthodontic force of 10 cN. The contralateral side served as control. After 6, 12, 72, 96, and 120 h groups of rats were killed. On parasagittal sections immunohistochemical staining was performed for analysis of HO-1 expression and quantification of osteoclasts. Orthodontic force induced a significant time-dependent HO-1 expression in mononuclear cells within the PDL at both the apposition- and resorption side. Shortly after placement of the orthodontic appliance HO-1 expression was highly induced in PDL cells but dropped to control levels within 72 h. Some osteoclasts were also HO-1 positive but this induction was shown to be independent of time- and mechanical stress. It is tempting to speculate that differential induction of tissue protecting- and osteoclast activating genes in the PDL determine the level of bone resorption and hyalinization and, subsequently, "fast" and "slow" tooth movers during orthodontic treatment.
正畸力会干扰牙周膜(PDL)的微环境,并诱导颅面骨重塑,这是牙齿移动所必需的。不幸的是,正畸牙齿移动常常受到PDL内缺血性损伤和细胞死亡(玻璃样变)以及牙根吸收的阻碍。已观察到玻璃样变和牙根吸收存在较大的个体差异,这可能是由于对玻璃样变的不同保护作用所致。血红素加氧酶-1(HO-1)通过将血红素分解为强抗氧化剂胆绿素/胆红素和信号分子一氧化碳,形成一种重要的保护机制。这些多功能的HO-1产物可保护机体免受缺血性和炎性损伤。我们推测在实验性牙齿移动过程中,正畸力会诱导PDL中HO-1的表达。本研究使用了25只6周龄的雄性Wistar大鼠。一侧的上三颗磨牙使用镍钛螺旋弹簧向近中移动,提供10 cN的持续正畸力。对侧作为对照。在6、12、72、96和120小时后处死每组大鼠。在矢状旁切片上进行免疫组织化学染色,以分析HO-1的表达并定量破骨细胞。正畸力在PDL内成骨和吸收侧的单核细胞中诱导了显著的时间依赖性HO-1表达。在放置正畸矫治器后不久,PDL细胞中HO-1的表达被高度诱导,但在72小时内降至对照水平。一些破骨细胞也呈HO-1阳性,但这种诱导显示与时间和机械应力无关。很容易推测,PDL中组织保护基因和破骨细胞激活基因的差异诱导决定了骨吸收和玻璃样变的程度,进而决定了正畸治疗期间“快”和“慢”的牙齿移动者。