Departments of Bacteriology, Hiroshima University Graduate School of Biomedical Sciences, Japan.
J Periodontal Res. 2011 Jun;46(3):389-95. doi: 10.1111/j.1600-0765.2011.01348.x. Epub 2011 Mar 1.
Aggregatibacter actinomycetemcomitans is one of the etiological pathogens implicated in the onset of periodontal disease. This pathogen produces cytolethal distending toxin (CDT) that acts as a genotoxin to induce cell cycle arrest and cellular distension in cultured cell lines. Therefore, CDT is a possible virulence factor; however, the in vivo activity of CDT on periodontal tissue has not been explored. Here, CDT was topically applied into the rat molar gingival sulcus; and the periodontal tissue was histologically and immunohistochemically examined.
Recombinant purified A. actinomycetemcomitans CDT was applied to gingival sulcus of male Wistar rats and tissue samples were immunohistochemmically examined.
One day after application, infiltration of neutrophils and dilation of blood vessels in the gingival connective tissue were found. At day three, desquamation and detachment of cells in the junctional epithelium was observed. This abrasion of junctional epithelium was not observed in rats treated with mutated CDT, in which a His274Ala mutation is present in the CdtB subunit. This indicates the tissue abrasion may be caused by the genotoxicity of CdtB. Expression of the proliferating cell nuclear antigen (PCNA), a marker for proliferating cells, was significantly suppressed using CDT treatment in the junctional epithelium and gingival epithelium.
Using the rat model, these data suggest CDT intoxication induces cell cycle arrest and damage in periodontal epithelial cells in vivo.
伴放线放线杆菌是引发牙周病的病因之一。该病原体产生细胞致死膨胀毒素(CDT),作为一种遗传毒素,诱导细胞周期停滞和细胞膨胀,这在培养的细胞系中已得到证实。因此,CDT 可能是一种致病因子;然而,CDT 在牙周组织中的体内活性尚未得到探索。本研究将 CDT 局部应用于大鼠磨牙牙龈沟,通过组织学和免疫组织化学检查牙周组织。
将重组纯化的 A. actinomycetemcomitans CDT 应用于雄性 Wistar 大鼠的牙龈沟,并用免疫组织化学方法检查组织样本。
应用后 1 天,在牙龈结缔组织中发现中性粒细胞浸润和血管扩张。第 3 天,观察到连接上皮细胞的脱落和分离。在应用突变型 CDT 的大鼠中未观察到这种连接上皮的磨损,突变型 CDT 的 CdtB 亚基中存在 His274Ala 突变。这表明组织磨损可能是由 CdtB 的遗传毒性引起的。在连接上皮和牙龈上皮中,用 CDT 处理后,增殖细胞核抗原(PCNA)的表达显著受到抑制,PCNA 是增殖细胞的标志物。
使用大鼠模型,这些数据表明 CDT 中毒会导致体内牙周上皮细胞的细胞周期停滞和损伤。