Matrix metalloproteinases-1 and -8 and TIMP-1 mRNA levels in normal and diseased human gingivae

被引:71
作者
Aiba, T
Akeno, N
Kawane, T
Okamoto, H
Horiuchi, N
机构
[1] OHU UNIV, SCH DENT, DEPT BIOCHEM, KORIYAMA, FUKUSHIMA 963, JAPAN
[2] OHU UNIV, SCH DENT, DEPT PERIODONTOL, KORIYAMA, FUKUSHIMA 963, JAPAN
关键词
matrix metalloproteinase-1; matrix metalloproteinase-8; tissue inhibitor of metalloproteinases-1; gene expression; periodontal disease;
D O I
10.1111/j.1600-0722.1996.tb00142.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
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.
引用
收藏
页码:562 / 569
页数:8
相关论文
共 38 条
[1]  
AINAMO J, 1975, INT DENT J, V25, P229
[2]   INDUCTION OF VITAMIN-D 24-HYDROXYLASE MESSENGER-RNA AND ACTIVITY BY 22-OXACALCITRIOL IN MOUSE KIDNEY AND DUODENUM - POSSIBLE ROLE IN DECREASE OF PLASMA 1-ALPHA,25-DIHYDROXYVITAMIN-D-3 [J].
AKENO, N ;
SAIKATSU, S ;
KIMURA, S ;
HORIUCHI, N .
BIOCHEMICAL PHARMACOLOGY, 1994, 48 (11) :2081-2090
[3]   THE GENE STRUCTURE OF TISSUE INHIBITOR OF METALLOPROTEINASES (TIMP)-3 AND ITS INHIBITORY ACTIVITIES DEFINE THE DISTINCT TIMP GENE FAMILY [J].
APTE, SS ;
OLSEN, BR ;
MURPHY, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14313-14318
[4]   ROLE OF CYTOKINES AND INFLAMMATORY MEDIATORS IN TISSUE DESTRUCTION [J].
BIRKEDALHANSEN, H .
JOURNAL OF PERIODONTAL RESEARCH, 1993, 28 (06) :500-510
[5]   ROLE OF MATRIX METALLOPROTEINASES IN HUMAN PERIODONTAL-DISEASES [J].
BIRKEDALHANSEN, H .
JOURNAL OF PERIODONTOLOGY, 1993, 64 (05) :474-484
[6]   PRIMARY STRUCTURE AND CDNA CLONING OF HUMAN FIBROBLAST COLLAGENASE INHIBITOR [J].
CARMICHAEL, DF ;
SOMMER, A ;
THOMPSON, RC ;
ANDERSON, DC ;
SMITH, CG ;
WELGUS, HG ;
STRICKLIN, GP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2407-2411
[7]  
FULLER HM, 1996, NATURE, V209, P728
[8]  
GOLDBERG GI, 1986, J BIOL CHEM, V261, P6600
[9]  
GOLUB LM, 1995, J CLIN PERIODONTOL, V22, P100
[10]   PATTERNS OF PROGRESSION AND REGRESSION OF ADVANCED DESTRUCTIVE PERIODONTAL-DISEASE [J].
GOODSON, JM ;
TANNER, ACR ;
HAFFAJEE, AD ;
SORNBERGER, GC ;
SOCRANSKY, SS .
JOURNAL OF CLINICAL PERIODONTOLOGY, 1982, 9 (06) :472-481