Immunohistochemical localization of MMP-2, MMP-9, TIMP-1, and TIMP-2 in the forming rat incisor

被引:54
作者
Goldberg, M
Septier, D
Bourd, K
Hall, R
George, A
Goldberg, H
Menashi, S
机构
[1] Univ Paris 05, Fac Chirurg Dentaire, Grp Matrices Extracellulaires & Biomineralisat, F-92120 Montrouge, France
[2] Univ Liverpool, Dept Clin Dent Sci, Liverpool Dent Sch, Liverpool L69 3BX, Merseyside, England
[3] Univ Illinois, Div Oral Biol, Chicago, IL USA
[4] Univ Western Ontario, Sch Dent, Fac Med & Dent, London, ON, Canada
[5] Univ Western Ontario, Dept Biochem, Fac Med & Dent, London, ON, Canada
[6] Hop St Louis, Paris, France
关键词
enamel; mantle dentin; MMPs; predentin; TIMPs;
D O I
10.1080/03008200390223927
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Western blots analyses and gelatin zymography established the presence of matrix metalloproteinase (MMP)-2 and -9 in the forming zone of rat incisor. Light microscope immunohistochemistry carried out on undemineralized material provided evidence for strong MMP-2 staining in the secretory ameloblasts, odontoblasts, in the enamel organ, and in the pulp. A weaker staining was observed in predentin and in the outer part of the forming enamel. Using MMP-9 antibodies, the staining was generally weak, except for the secretory ameloblasts that were positively stained. Electron microscopic immunohistochemistry of undemineralized sections revealed a close association between gold-antibodies complexes and cytoskeletal microfilaments in the cytosol of secretory ameloblasts and odontoblasts, within the rough endoplasmic reticulum and along the plasma membrane. The striking feature of MMP-2 and -9 electron immunostaining was the particularly high labeling in the mantle dentin. By contrast, staining of tissue inhibitors of metalloproteinases (TIMP-1 and -2) was lowest in this region. We suggest that this uneven distribution may have some functional implications.
引用
收藏
页码:143 / 153
页数:11
相关论文
共 50 条
  • [1] Molecular cloning and mRNA tissue distribution of a novel matrix metalloproteinase isolated from porcine enamel organ
    Bartlett, JD
    Simmer, JP
    Xue, J
    Margolis, HC
    Moreno, EC
    [J]. GENE, 1996, 183 (1-2) : 123 - 128
  • [2] PROTEOLYTIC ACTIVITY OF DEVELOPING DENTIN OF RAT TOOTH GERMS REVEALED BY THE GELATIN-FILM SUBSTRATE TECHNIQUE
    BETTI, F
    KATCHBURIAN, E
    [J]. ARCHIVES OF ORAL BIOLOGY, 1982, 27 (10) : 891 - 896
  • [3] PROTEOLYTIC REMODELING OF EXTRACELLULAR-MATRIX
    BIRKEDALHANSEN, H
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (05) : 728 - 735
  • [4] Structural properties of matrix metalloproteinases
    Bode, W
    Fernandez-Catalan, C
    Tschesche, H
    Grams, F
    Nagase, H
    Maskos, K
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (04) : 639 - 652
  • [5] MATRIX METALLOPROTEINASES AND TIMP-1 LOCALIZATION AT SITES OF OSTEOGENESIS IN THE CRANIOFACIAL REGION OF THE RABBIT EMBRYO
    BRECKON, JJW
    HEMBRY, RM
    REYNOLDS, JJ
    MEIKLE, MC
    [J]. ANATOMICAL RECORD, 1995, 242 (02): : 177 - 187
  • [6] Tissue inhibitors of metalloproteinases: evolution, structure and function
    Brew, K
    Dinakarpandian, D
    Nagase, H
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1477 (1-2): : 267 - 283
  • [7] Specificity controls for immunocytochemical methods
    Burry, RW
    [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (02) : 163 - 165
  • [8] Expression and localization of membrane type 1 matrix metalloproteinase in tooth tissues
    Caron, C
    Xue, J
    Bartlett, JD
    [J]. MATRIX BIOLOGY, 1998, 17 (07) : 501 - 511
  • [9] SEPARATION BY POLYACRYLAMIDE-GEL ELECTROPHORESIS OF MULTIPLE PROTEASES IN RAT AND BOVINE ENAMEL
    DENBESTEN, PK
    HEFFERNAN, LM
    [J]. ARCHIVES OF ORAL BIOLOGY, 1989, 34 (06) : 399 - 404
  • [10] DENBESTEN PK, 1989, TOOTH ENAMEL, V5, P278