Department of Periodontology, Institute of Dentistry, University of Turku, Turku, Finland.
J Periodontol. 2012 Oct;83(10):1329-35. doi: 10.1902/jop.2012.110535. Epub 2012 Jan 16.
Effects of Fusobacterium nucleatum (F. nucleatum) biofilm on epithelial cell proliferation, apoptotic cell death, and basement membrane constituent collagen IV production were examined in an organotypic dento-epithelial (OD-E) model.
The OD-E model was constructed by seeding keratinocytes on fibroblast-containing collagen gels and by placing tooth pieces on top. A 3-day-old biofilm either a laboratory strain (American Type Culture Collection [ATCC] 25586) or a clinical strain (Anaerobe Helsinki Negative [AHN] 9508) of F. nucleatum was placed on the top of the model. The coculture was incubated ≤24 hours. The expression and localization of Ki-67, caspase-3, and collagen IV were examined by immunohistochemistry.
Hematoxylin and eosin staining showed epithelial migration and lateral sprouting into the connective tissue matrix in F. nucleatum OD-E cocultures. The proliferation pattern of the in vitro dento-epithelial junction was changed. In controls without bacterial challenge, the Ki-67 expression was abundant in the cells attached to the tooth, whereas in F. nucleatum biofilm-treated cultures, the Ki-67-expressing cells were more often in the connective tissue-facing side of the epithelium. An apoptotic marker caspase-3 was expressed in controls and in F. nucleatum laboratory strain ATCC cocultures throughout the epithelium, in contrast to cultures treated with F. nucleatum clinical strain AHN, in which caspase-3 was absent. Collagen IV stainings were negative in both controls and F. nucleatum cocultures.
F. nucleatum biofilm coculture with OD-E model causes lateral sprouting of the epithelium with an altered epithelial proliferation pattern, resembling the histologic changes seen in vivo in the early pathogenesis of periodontal disease.
本研究通过建立牙上皮组织模型(OD-E 模型),检测具核梭杆菌(F. nucleatum)生物膜对上皮细胞增殖、凋亡细胞死亡和基底膜成分 IV 型胶原产生的影响。
通过将角质形成细胞接种在含有成纤维细胞的胶原凝胶上,并在上部放置牙块来构建 OD-E 模型。在模型的顶部放置实验室菌株(美国典型培养物保藏中心 [ATCC] 25586)或临床菌株(厌氧赫尔辛基阴性 [AHN] 9508)的 3 天龄生物膜。将共培养物孵育≤24 小时。通过免疫组织化学检查 Ki-67、半胱氨酸天冬氨酸蛋白酶-3 和 IV 型胶原的表达和定位。
苏木精和伊红染色显示在具核梭杆菌 OD-E 共培养物中上皮细胞迁移和侧向分支进入结缔组织基质。体外牙上皮连接的增殖模式发生改变。在没有细菌挑战的对照中,Ki-67 表达丰富的细胞附着在牙齿上,而在具核梭杆菌生物膜处理的培养物中,Ki-67 表达的细胞更常见于上皮组织面向的一侧。凋亡标志物 caspase-3 在对照和具核梭杆菌实验室菌株 ATCC 共培养物中均有表达,而在具核梭杆菌临床菌株 AHN 处理的培养物中则没有。两种对照和具核梭杆菌共培养物的 IV 型胶原染色均为阴性。
具核梭杆菌生物膜与 OD-E 模型共培养可导致上皮侧向分支,上皮增殖模式发生改变,类似于牙周病早期发病过程中体内所见的组织学变化。