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
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