Inhibition of mitosis and induction of apoptosis in MG63 human osteosarcoma-derived cells in vitro by surface proteins from Actinobacillus actinomycetemcomintans

被引:6
作者
Gadhavi, A
Wilson, M
Tabona, P
Newman, HN
Henderson, B
Bennett, JH
机构
[1] UCL, Eastman Dent Inst, Dept Oral Pathol, London WC1X 8LD, England
[2] UCL, Eastman Dent Inst, Clin Res Ctr, London WC1X 8LD, England
[3] UCL, Eastman Dent Inst, Dept Microbiol, London WC1X 8LD, England
[4] UCL, Eastman Dent Inst, Dept Periodontol, London WC1X 8LD, England
[5] UCL, Eastman Dent Inst, Cellular Microbiol Res Grp, London WC1X 8LD, England
关键词
MG63; cells; apoptosis; mitosis; Actinobacillus actinomycetemcomintans;
D O I
10.1016/S0003-9969(00)00028-5
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Gentle saline extraction releases a heterogeneous mixture of proteins associated with the cell surface of Actinobacillus actinomycetemcomintans, termed the surface protein fraction (SF). Some SF components are biologically active and may modulate cell behaviour in a manner of putative importance in the aetiology of periodontitis. To further characterize this activity, the ability of the SF to induce mitosis and apoptosis in MG63 cells was investigated. Cells were plated at 10(3)-10(4) cells/cm(2) and allowed to attach before culture in the serum-free medium in the presence of 25 mu g/ml SF for 2-24 h. The apoptotic and mitotic figures present were counted and the results expressed as an apoptotic or mitotic index. The apoptotic and mitotic compartments were very small, but there was an inverse correlation between mitosis and apoptosis. In control experiments the mitotic was higher than the apoptotic index, whilst in the presence of SF this was reversed. These results were confirmed using in situ end-labelling. SF, therefore, may stimulate apoptotic, but inhibit mitotic, activity in MG63 cells. This raises the possibility that components of SF might induce subtle changes in the balance between apoptosis and mitosis, which, in turn, could contribute to the progression of periodontitis. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:707 / 711
页数:5
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