Cell division, synthetic capacity and apoptosis in periodontal lesions analysed by in situ hybridisation and immunohistochemistry

Citation
O. Koulouri et al., Cell division, synthetic capacity and apoptosis in periodontal lesions analysed by in situ hybridisation and immunohistochemistry, J CLIN PER, 26(8), 1999, pp. 552-559
Citations number
37
Categorie Soggetti
Dentistry/Oral Surgery & Medicine","da verificare
Journal title
JOURNAL OF CLINICAL PERIODONTOLOGY
ISSN journal
03036979 → ACNP
Volume
26
Issue
8
Year of publication
1999
Pages
552 - 559
Database
ISI
SICI code
0303-6979(199908)26:8<552:CDSCAA>2.0.ZU;2-1
Abstract
In this study, we investigated the synthetic and proliferative activity of infiltrating mononuclear cells in sections of granulation tissue from perio dontitis lesions in both adult periodontitis (AP) and early onset periodont itis (EOP) patients. We also investigated the role of apoptosis in the remo delling of the inflamed tissue. We utilised a Ki-67 antigen specific antibo dy and a histone messenger RNA (mRNA) probe to detect cells undergoing cell division in the sections, Oligonucleotide probes for 28S ribosomal RNA and for the detection of poly A mRNA were utilised to detect cells with synthe tic capacity. Apoptosis was determined using terminal transferase labelling of fragmented DNA with Biotin labelled dUTP. Biopsies of granulation tissu e were obtained from 9 AP patients, from 10 EOP patients and for comparativ e purposes, biopsies of gingival tissue from 4 patients with AP. There were no differences regarding the relative proportions of cells with synthetic capacity or in the numbers of dividing cells in the periodontitis tissue se ctions. However, we observed an increase in the number of dividing cells in the AP granulation tissues compared to the AP gingival sections and that t hese cells were predominantly fibroblast like in appearance. Apoptotic cell s consisted mainly of connective tissue cells; mainly fibroblasts with few if any leukocytes being apoptotic other than polymorphonuclear leukocytes. Only a few cyto-phagocytic macrophages were ever observed in the gingival a nd granulation tissues. We conclude that the turnover of infiltrating leuko cytes in inflamed periodontal tissue is low, that they probably arrive at t his site by recruitment from distant lymph nodes, and that neither cell div ision nor programmed cell death significantly alter the numbers of inflamma tory cells. On the other hand, fibroblast apoptosis and cell division occur within the periodontium as these are typical processes in the normal turno ver and remodelling of these tissues.