Aiba T, Akeno N, Kawane T, Okamoto H, Horiuchi N
Department of Biochemistry, Ohu University School of Dentistry, Koriyama, Japan.
Eur J Oral Sci. 1996 Oct-Dec;104(5-6):562-9. doi: 10.1111/j.1600-0722.1996.tb00142.x.
Interstitial collagenases, including matrix metalloproteinase-1 (MMP-1) and -8 (MMP-8), serve as initiators of extracellular matrix destruction in periodontal disease. Collagenase activities are mainly regulated by tissue inhibitors of metalloproteinases (TIMPs). We tested the effects of inflammation on MMP-1 and MMP-8 gene expression in periodontal disease. To determine the relative abundance of these mRNAs in gingiva, we used a reverse transcription-polymerase chain reaction (RT-PCR) assay. Gingival biopsies were divided into 2 groups; a control group and an inflamed group with severe gingivitis or periodontitis. The MMP-1 mRNA levels were significantly elevated in inflamed gingiva, while the levels of the MMP-8 transcript were not different in the 2 groups and barely detectable by RT-PCR assay. The expression of the TIMP-1 gene was not altered, and remained higher than any of these other genes in both control and diseased gingivae. These results suggest that MMP-1 rather than MMP-8 may play an important role in the initiation of collagen degradation in periodontal disease. However, the possibility remains that MMP-8 plays an important role in periodontal tissue destruction, since the mRNA abundance and not the enzyme activity was assessed.
间质胶原酶,包括基质金属蛋白酶-1(MMP-1)和-8(MMP-8),是牙周病中细胞外基质破坏的启动因子。胶原酶活性主要受金属蛋白酶组织抑制剂(TIMPs)调节。我们测试了炎症对牙周病中MMP-1和MMP-8基因表达的影响。为了确定这些mRNA在牙龈中的相对丰度,我们使用了逆转录-聚合酶链反应(RT-PCR)检测法。牙龈活检组织分为两组:对照组和患有严重牙龈炎或牙周炎的炎症组。炎症牙龈中MMP-1 mRNA水平显著升高,而MMP-8转录本水平在两组中无差异,通过RT-PCR检测几乎检测不到。TIMP-1基因的表达未改变,在对照和患病牙龈中均高于其他任何基因。这些结果表明,在牙周病中胶原降解的起始过程中,MMP-1而非MMP-8可能起重要作用。然而,由于评估的是mRNA丰度而非酶活性,MMP-8在牙周组织破坏中起重要作用的可能性仍然存在。