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核梭杆菌在体外重建人牙龈中的深度侵袭有限。

Limited in-depth invasion of Fusobacterium nucleatum into in vitro reconstructed human gingiva.

机构信息

The Gade Institute, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway.

出版信息

Arch Oral Biol. 2012 Apr;57(4):344-51. doi: 10.1016/j.archoralbio.2011.09.015. Epub 2011 Oct 24.

Abstract

OBJECTIVE

Fusobacterium nucleatum is an opportunistic pathogen with a key role in subgingival plaque formation and it is found in increased numbers in periodontally affected sites. This study aimed to investigate the potential of F. nucleatum to penetrate and induce alterations in an in vitro reconstructed human gingival mucosa model.

METHODS

Three-dimensional (3D) organotypic models of human gingiva were engineered using primary gingival keratinocytes and fibroblasts. The reconstructed tissues were challenged with four different strains of fluorescently labelled F. nucleatum in suspension placed on top of epithelial layers. Confocal laser scanning was used to assess the presence of fusobacteria through the organotypic model. Apoptosis (cleaved caspase-3) and cell proliferation (Ki-67) were evaluated by the use of immunohistochemistry in 3D-tissue models. Quantitative real-time PCR was performed to investigate the mRNA expression for MMP-13 and E-cadherin in both 3D-tissues and monolayers.

RESULTS

F. nucleatum invaded the superficial epithelial layers of gingival 3D-tissue models. Challenged tissues showed accentuated shedding of superficial layers and increased number of cleaved caspase-3 and Ki-67 positive cells than controls, although not statistically significant. Levels of E-cadherin and MMP-13 mRNA were not significantly perturbed in multilayer culture. A variable and disproportionate response of MMP-13 mRNA level resulted in challenged primary keratinocytes in monolayers, compared to multilayer culture.

CONCLUSION

These results indicate that F. nucleatum is able to invade superficially a differentiated, stratified gingival epithelium in vitro and triggers the efficient elimination of bacterial infection through epithelial shredding without causing a permanent damage of the tissue.

摘要

目的

具核梭杆菌是一种机会性病原体,在龈下菌斑形成中起关键作用,并且在牙周病变部位数量增加。本研究旨在探讨具核梭杆菌穿透和诱导体外重建人牙龈黏膜模型改变的潜力。

方法

使用原代牙龈角质形成细胞和成纤维细胞构建三维(3D)人牙龈器官型模型。将四种不同荧光标记的具核梭杆菌悬液置于上皮层上方,对重建组织进行挑战。通过共聚焦激光扫描评估具核梭杆菌在器官型模型中的存在。通过免疫组织化学在 3D 组织模型中评估细胞凋亡(裂解的 caspase-3)和细胞增殖(Ki-67)。通过定量实时 PCR 检测 MMP-13 和 E-钙黏蛋白在 3D 组织和单层中的 mRNA 表达。

结果

具核梭杆菌侵入牙龈 3D 组织模型的浅层上皮层。与对照组相比,受挑战的组织显示出浅层脱落加剧,并且裂解的 caspase-3 和 Ki-67 阳性细胞数量增加,但无统计学意义。在多层培养中,E-钙黏蛋白和 MMP-13 mRNA 水平没有明显改变。与多层培养相比,单层培养中受挑战的原代角质形成细胞的 MMP-13 mRNA 水平表现出不同的、不成比例的反应。

结论

这些结果表明,具核梭杆菌能够在体外穿透分化的、分层的牙龈上皮,并通过上皮碎片有效地消除细菌感染,而不会对组织造成永久性损伤。

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