Histochemical and immunohistochemical evaluation of gingival collagen and metalloproteinases in peri-implantitis

被引:35
作者
Borsani, E
Salgarello, S
Mensi, M
Boninsegna, R
Stacchiotti, A
Rezzani, R
Sapelli, P
Bianchi, R
Rodella, LF
机构
[1] Univ Brescia, Dept Biomed Sci & Biotechnol, Div Human Anat, I-25123 Brescia, Italy
[2] Univ Brescia, Dent Sch, I-25121 Brescia, Italy
关键词
extracellular matrix; gingiva; metalloproteinases; collagen; immunohistochemistry; peri-implantitis;
D O I
10.1016/j.acthis.2005.06.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The extra-cellular matrix of the gingival tissue plays an important rote in the homeostasis of dental implants. In this work we have studied immunohistochemically the distribution of collagen I-III-IV-V, tenascin, metalloproteinases (MMP) 1-3-8-13 and TIMP-1 in three groups of patients: (1) subjects with natural teeth (healthy periodontal tissue), (2) subjects with normal peri-implant mucosa and (3) subjects with clinically evident peri-implantitis. The immunolabelling for collagen I-III-IV showed a similar pattern in at[ three groups. The [abetting for collagen V increased in lamina propria of healthy peri-implant tissue and peri-implantitis. Tenascin immunolabelling in healthy and peri-implant tissues was scattered in lamina propria. In peri-implantitis tenascin immunolabelling increased mainly near to the basal lamina. The MMP-1-3-8 and TIMP-1 immunolabelling were very faint and localized in the stroma in all three groups. In healthy and peri-implant tissues MMP-13 immunolabelling was found in the lamina propria whereas in peri-implantitis MMP13 immunolabelling was also in epithelium. On the whole, these data suggest that in the extracellular matrix of peri-implantitis there are alterations of collagen V, tenascin and MMP-13 patterns. (c) 2005 Elsevier GmbH. All rights reserved.
引用
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页码:231 / 240
页数:10
相关论文
共 68 条
[1]  
ALEXANDER MB, 1994, CURR OPIN PERIODONT, V1, P39
[2]   Longitudinal evaluation of GCF MMP-3 and TIMP-1 levels as prognostic factors for progression of periodontitis [J].
Alpagot, T ;
Bell, C ;
Lundergan, W ;
Chambers, DW ;
Rudin, R .
JOURNAL OF CLINICAL PERIODONTOLOGY, 2001, 28 (04) :353-359
[3]   Metalloproteinase inhibitors: biological actions and therapeutic opportunities [J].
Baker, AH ;
Edwards, DR ;
Murphy, G .
JOURNAL OF CELL SCIENCE, 2002, 115 (19) :3719-3727
[4]  
Bergback B., 2001, WATER AIR SOIL POLL, V1, P3, DOI DOI 10.1023/A:1017531532576
[5]   The soft tissue barrier at implants and teeth [J].
Berglundh, T. ;
Lindhe, J. ;
Ericsson, I. ;
Marinello, C. P. ;
Liljenberg, B. ;
Thomsen, P. .
CLINICAL ORAL IMPLANTS RESEARCH, 1991, 2 (02) :81-90
[6]   MATRIX METALLOPROTEINASES - A REVIEW [J].
BIRKEDALHANSEN, H ;
MOORE, WGI ;
BODDEN, MK ;
WINDSOR, LJ ;
BIRKEDALHANSEN, B ;
DECARLO, A ;
ENGLER, JA .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1993, 4 (02) :197-250
[7]   ROLE OF CYTOKINES AND INFLAMMATORY MEDIATORS IN TISSUE DESTRUCTION [J].
BIRKEDALHANSEN, H .
JOURNAL OF PERIODONTAL RESEARCH, 1993, 28 (06) :500-510
[8]   ROLE OF MATRIX METALLOPROTEINASES IN HUMAN PERIODONTAL-DISEASES [J].
BIRKEDALHANSEN, H .
JOURNAL OF PERIODONTOLOGY, 1993, 64 (05) :474-484
[9]   NEW COLLAGENS, NEW CONCEPTS [J].
BURGESON, RE .
ANNUAL REVIEW OF CELL BIOLOGY, 1988, 4 :551-577
[10]   CONNECTIVE-TISSUE ORGANIZATION OF HEALTHY-HUMAN GINGIVA - ULTRASTRUCTURAL-LOCALIZATION OF COLLAGEN TYPES-I-III-IV [J].
CHAVRIER, C ;
COUBLE, ML ;
MAGLOIRE, H ;
GRIMAUD, JA .
JOURNAL OF PERIODONTAL RESEARCH, 1984, 19 (03) :221-229