Simvastatin, an HMG-CoA reductase inhibitor, reduced the expression of matrix metalloproteinase-9 (Gelatinase B) in osteoblastic cells and HT1080 fibrosarcoma cells

被引:44
作者
Thunyakitpisal, PD
Chaisuparat, R
机构
[1] Chulalongkorn Univ, Fac Dent, Dept Anat, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Fac Dent, Dept Oral Pathol, Bangkok 10330, Thailand
关键词
HT1080; matrix metalloproteinase-9; osteoblast; simvastatin; tumor necrosis factor-alpha;
D O I
10.1254/jphs.94.403
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MMP-9 or Gelatinase B, a member of the matrix metalloproteinase family (MMPs), plays important roles in physiological events such as tissue remodeling and in pathological processes that lead to destructive bone diseases, including osteoarthritis and periodontitis. In addition to its effect on the increase of total bone mass, statin (an HMG-CoA reductase inhibitor) suppresses the expression of MMPs. In this study, we proposed that simvastatin reduces MMP-9 expression in osteoblasts and HT1080 fibrosarcoma cell line. Gelatin zymography, Western blot analysis and reverse transcriptase-PCR were used to investigate the effects of simvastatin on MMP-9 in primary calvaria cells, U2-OS osteosarcoma cells, and HT1080 fibrosarcoma cells. The results from gelatin zymography and Western blot analysis revealed that simvastatin suppressed MMP-9 activity in these cells in concentration- and time-dependent manners. The effective concentrations of simvastatin were 100-500 nM, 5-15 muM, and 2.5-10 muM in primary calvaria, U2-OS, and HT1080 cells, respectively. Collectively, these results suggest that simvastatin is a potent drug for inhibition of MMP-9 expression in osteoblastic cells and HT1080 fibrosarcoma cells.
引用
收藏
页码:403 / 409
页数:7
相关论文
共 42 条
  • [1] Expression of matrix metalloproteinase 9 (96-kd gelatinase B) in human rheumatoid arthritis
    Ahrens, D
    Koch, AE
    Pope, RM
    SteinPicarella, M
    Niedbala, MJ
    [J]. ARTHRITIS AND RHEUMATISM, 1996, 39 (09): : 1576 - 1587
  • [2] FACTORS THAT PROMOTE PROGRESSIVE DEVELOPMENT OF THE OSTEOBLAST PHENOTYPE IN CULTURED FETAL-RAT CALVARIA CELLS
    ARONOW, MA
    GERSTENFELD, LC
    OWEN, TA
    TASSINARI, MS
    STEIN, GS
    LIAN, JB
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 143 (02) : 213 - 221
  • [3] BELLOSTA S, 2000, ARTERIOSCLER THROMB, V18, P1671
  • [4] ROLE OF MATRIX METALLOPROTEINASES IN HUMAN PERIODONTAL-DISEASES
    BIRKEDALHANSEN, H
    [J]. JOURNAL OF PERIODONTOLOGY, 1993, 64 (05) : 474 - 484
  • [5] BROWN SM, 1987, J BIOL CHEM, V253, P1121
  • [6] CHAMBERS TJ, 1985, J CELL SCI, V76, P155
  • [7] Inhibitors of hydroxymethylglutaryl-coenzyme A reductase and risk of fracture among older women
    Chan, KA
    Andrade, SE
    Boles, M
    Buist, DSM
    Chase, GA
    Donahue, JG
    Goodman, MJ
    Gurwitz, JH
    LaCroix, AZ
    Platt, R
    [J]. LANCET, 2000, 355 (9222) : 2185 - 2188
  • [8] CHEN QJ, 1998, BONE, V23, pS548
  • [9] HMG-CoA reductase inhibitors increase BMD in type 2 diabetes mellitus patients
    Chung, YS
    Lee, MD
    Lee, SK
    Kim, HM
    Fitzpatrick, LA
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (03) : 1137 - 1142
  • [10] Proteinases in bone resorption:: obvious and less obvious roles
    Delaissé, JM
    Engsig, MT
    Everts, V
    Ovejero, MD
    Ferreras, M
    Lund, L
    Vu, TH
    Werb, Z
    Winding, B
    Lochter, A
    Karsdal, MA
    Troen, T
    Kirkegaard, T
    Lenhard, T
    Heegaard, AM
    Neff, L
    Baron, R
    Foged, NT
    [J]. CLINICA CHIMICA ACTA, 2000, 291 (02) : 223 - 234