Koulouri O, Lappin D F, Radvar M, Kinane D F
Periodontology Unit, Glasgow Dental Hospital and School, Scotland, UK.
J Clin Periodontol. 1999 Aug;26(8):552-9. doi: 10.1034/j.1600-051x.1999.260810.x.
In this study, we investigated the synthetic and proliferative activity of infiltrating mononuclear cells in sections of granulation tissue from periodontitis lesions in both adult periodontitis (AP) and early onset periodontitis (EOP) patients. We also investigated the role of apoptosis in the remodelling of the inflamed tissue. We utilised a Ki-67 antigen specific antibody 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 synthetic capacity. Apoptosis was determined using terminal transferase labelling of fragmented DNA with Biotin labelled dUTP. Biopsies of granulation tissue were obtained from 9 AP patients, from 10 EOP patients and for comparative 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 sections. However, we observed an increase in the number of dividing cells in the AP granulation tissues compared to the AP gingival sections and that these cells were predominantly fibroblast like in appearance. Apoptotic cells 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 and granulation tissues. We conclude that the turnover of infiltrating leukocytes in inflamed periodontal tissue is low, that they probably arrive at this site by recruitment from distant lymph nodes, and that neither cell division nor programmed cell death significantly alter the numbers of inflammatory cells. On the other hand, fibroblast apoptosis and cell division occur within the periodontium as these are typical processes in the normal turnover and remodelling of these tissues.
在本研究中,我们调查了成人牙周炎(AP)和早发性牙周炎(EOP)患者牙周炎病变肉芽组织切片中浸润单核细胞的合成和增殖活性。我们还研究了细胞凋亡在炎症组织重塑中的作用。我们使用Ki-67抗原特异性抗体和组蛋白信使核糖核酸(mRNA)探针来检测切片中正在进行细胞分裂的细胞。用于28S核糖体RNA和检测聚腺苷酸mRNA的寡核苷酸探针被用于检测具有合成能力的细胞。使用生物素标记的dUTP对断裂DNA进行末端转移酶标记来确定细胞凋亡。从9例AP患者、10例EOP患者获取肉芽组织活检样本,为作比较,还从4例AP患者获取牙龈组织活检样本。在牙周炎组织切片中,具有合成能力的细胞相对比例或分裂细胞数量并无差异。然而,我们观察到,与AP牙龈切片相比,AP肉芽组织中分裂细胞数量增加,且这些细胞在外观上主要类似成纤维细胞。凋亡细胞主要由结缔组织细胞组成;主要是成纤维细胞,除多形核白细胞外,几乎没有白细胞发生凋亡。在牙龈和肉芽组织中仅观察到少数细胞吞噬性巨噬细胞。我们得出结论,炎症牙周组织中浸润白细胞的更替率较低,它们可能是从远处淋巴结募集而来到达该部位的,细胞分裂和程序性细胞死亡均未显著改变炎症细胞数量。另一方面,成纤维细胞凋亡和细胞分裂发生在牙周组织内,因为这些是这些组织正常更替和重塑的典型过程。