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Suture compression induced bone resorption with intensified MMP-1 and 13 expressions

机译:缝线压缩诱导的骨吸收增强MMP-1和13表达

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Suture compression is a widely used approach to inhibit maxillary growth; however, biological responses in sutures to compressive force are still unclear. The objective of this pilot study was to investigate the matrix metalloproteinase (MMP) expression and osteoclast activities during the midpalatal suture compression. Methods: 56 six-week old male C57BL/6 mice were randomly assigned to the control and compression groups. The mice in the compression and control groups received helix springs bonded to the maxillary molars delivering initial compressive forces of 0.20 and 0. N (no activation), respectively. On Days 1, 4, 7 and 14, animals were sacrificed and scanned using micro-computed tomography to quantify suture width and bone mineral density. Serial histological sections were stained with HE, TRAP, and immunohistochemistry to observe changes in bone resorption, osteoclast activities, and MMP-1, 8, and 13 expressions. Bone volume/total volume (Bv/Tv) ratio, osteoclast count, osteoclast covering area, and MMP expression intensity were measured. The Mann-Whitney and the Kruskal-Wallis tests with Bonferroni post-hoc corrections were performed to compare differences between groups and between time points in the same group at significant level of P < 0.05. Results: Compared to the control, suture width in the compression group was significantly reduced on Day 1, but continuously widened with reduced bone mineral density afterwards. With MMP-1 and -13 evidently intensified expressions, osteoclast number and activities significantly increased, leading to reduced Bv/Tv ratio and progressive bone resorption from Days 4 to 14. Conclusions: Suture compression elevated the MMP-1 and 13 expressions, activated osteoclasts, reduced bone density, and induced bone resorption adjacent to the suture. It suggests that suture compression can be used for bone volume reduction.
机译:缝合加压是一种广泛使用的抑制上颌骨生长的方法。然而,缝合线对压缩力的生物学反应仍不清楚。这项初步研究的目的是研究pal中缝缝合压迫过程中基质金属蛋白酶(MMP)的表达和破骨细胞活性。方法:将56只六周大的雄性C57BL / 6小鼠随机分为对照组和压缩组。压缩组和对照组中的小鼠接受螺旋弹簧,这些螺旋弹簧结合到上颌磨牙上,分别提供0.20和0. N(无激活)的初始压缩力。在第1、4、7和14天,处死动物,并使用微型计算机断层扫描技术进行扫描,以量化缝线宽度和骨矿物质密度。连续组织切片用HE,TRAP和免疫组化染色,观察骨吸收,破骨细胞活性以及MMP-1、8和13表达的变化。测量骨体积/总体积(Bv / Tv)比,破骨细胞计数,破骨细胞覆盖面积和MMP表达强度。进行Bonferroni事后校正的Mann-Whitney和Kruskal-Wallis检验,以P <0.05的显着水平比较组之间以及同一组时间点之间的差异。结果:与对照组相比,压迫组的缝线宽度在第1天显着减少,但随后逐渐扩大,随后骨矿物质密度降低。从第4天到第14天,随着MMP-1和-13的表达明显增强,破骨细胞的数量和活性显着增加,导致Bv / Tv比值降低和进行性骨吸收。结论:缝合压迫提高了MMP-1和13的表达,活化了破骨细胞,降低骨密度,并在缝合线附近引起骨吸收。这表明缝线压缩可用于减少骨量。

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