Takahashi I, Nishimura M, Onodera K, Bae J-W, Mitani H, Okazaki M, Sasano Y, Mitani H
Division of Orthodontics and Dentofacial Orthopedics, Tohoku University Graduate School of Dentistry, Sendai, Japan.
J Dent Res. 2003 Aug;82(8):646-51. doi: 10.1177/154405910308200815.
Periodontal ligament tissue is remodeled on both the tension and compression sides of moving teeth during orthodontic tooth movement. The present study was designed to clarify the hypothesis that the expression of MMP-8 and MMP-13 mRNA is promoted during the remodeling of periodontal ligament tissue in orthodontic tooth movement. We used the in situ hybridization method and semi-quantitative reverse-transcription/polymerase chain-reaction analysis to elucidate the gene expression of MMP-8 and MMP-13 mRNA. Expression of MMP-8 and MMP-13 mRNA transiently increased on both the compression and tension sides during active tooth movement in vivo. The gene expression of MMP-8 and MMP-13 was induced by tension, while compression indirectly promoted the gene expression of MMP-8 and MMP-13 through soluble factors in vitro. Thus, we concluded that the expression of MMP-8 and MMP-13 is differentially regulated by tension and compression, and plays an important role in the remodeling of the periodontal ligament.
在正畸牙齿移动过程中,牙周膜组织在移动牙齿的张力侧和压力侧都会发生重塑。本研究旨在阐明以下假设:在正畸牙齿移动过程中牙周膜组织重塑期间,MMP - 8和MMP - 13 mRNA的表达会增加。我们使用原位杂交方法和半定量逆转录/聚合酶链反应分析来阐明MMP - 8和MMP - 13 mRNA的基因表达。在体内牙齿主动移动过程中,MMP - 8和MMP - 13 mRNA在压力侧和张力侧的表达均短暂增加。MMP - 8和MMP - 13的基因表达由张力诱导,而在体外,压力通过可溶性因子间接促进MMP - 8和MMP - 13的基因表达。因此,我们得出结论,MMP - 8和MMP - 13的表达受张力和压力的差异调节,并在牙周膜重塑中起重要作用。