Faculty of Dentistry, National University of Singapore, Singapore 119085, Singapore.
Institute for Health Innovation and Technology (iHealthtech), National University of Singapore, Singapore 117599, Singapore.
Biofabrication. 2023 Aug 2;15(4). doi: 10.1088/1758-5090/ace935.
Gingival connective tissue and its vasculature play a crucial role in the host's immune response against the periodontal microbiome and serve as a bridge between the oral and systemic environments. However, there is a lack of representative models that mimic the complex features of vascularized gingival connective tissue and its interaction with the periodontal microbiome, hindering our understanding of periodontal health and disease. Towards this pursuit, we present the characterization of vascularized gingival connective tissue equivalents (CTEs) as a model to study the interactions between oral biofilm colonizers and gingival tissues in healthy and diseased states. Whole-mount immunolabeling and label-free confocal reflectance microscopy of human fibrin-based matrix embedded with gingival fibroblasts and microvascular endothelial cells demonstrated the generation of bi-cellular vascularized gingival CTEs. Next, we investigated the response of the vascularized gingival CTEs to early, intermediate, and late oral biofilm colonizers. Despite colonization, the early colonizers did not elicit any significant change in the production of the cytokines and chemokines by the CTEs representative of the commensal and homeostatic state. In contrast, intermediate and late colonizers representing a transition to a diseased state exhibited connective tissue and vascular invasion, and elicited a differential immune response accompanied by increased monocyte migration. The culture supernatants produced by the vascularized gingival CTEs in response to early and intermediate colonizers polarized macrophages towards an immunomodulatory M2-like phenotype which activates and protects the host, while the late colonizers polarized towards a pro-inflammatory M1-like phenotype. Lastly,analysis showed a high strength of associations between the proteins and transcripts investigated with periodontitis and vascular diseases. In conclusion, the vascularized gingival CTEs provide a biomimeticplatform to study host-microbiome interactions and innate immune response in periodontal health and diseased states, which potentially paves the way toward the development and assessment of novel periodontal therapeutics.
牙龈结缔组织及其脉管系统在宿主对牙周微生物组的免疫反应中起着至关重要的作用,并充当口腔和全身环境之间的桥梁。然而,目前缺乏能够模拟血管化牙龈结缔组织复杂特征及其与牙周微生物组相互作用的代表性模型,这阻碍了我们对牙周健康和疾病的理解。针对这一目标,我们提出了血管化牙龈结缔组织等效物(CTE)的特征描述,作为研究口腔生物膜定植者与健康和患病状态下牙龈组织相互作用的模型。对人纤维蛋白基质中嵌入的牙龈成纤维细胞和微血管内皮细胞进行全组织免疫标记和无标记共聚焦反射显微镜分析,证明了双细胞血管化牙龈 CTE 的生成。接下来,我们研究了血管化牙龈 CTE 对早期、中期和晚期口腔生物膜定植者的反应。尽管定植,但早期定植者不会引起 CTE 产生细胞因子和趋化因子的任何显著变化,这些细胞因子和趋化因子代表了共生和稳态状态。相比之下,代表向疾病状态过渡的中期和晚期定植者表现出结缔组织和血管侵袭,并引发了伴随单核细胞迁移增加的差异免疫反应。血管化牙龈 CTE 对早期和中期定植者产生的培养上清液使巨噬细胞向具有免疫调节作用的 M2 样表型极化,从而激活和保护宿主,而晚期定植者则向促炎的 M1 样表型极化。最后,分析表明,所研究的蛋白质和转录物与牙周炎和血管疾病之间存在很强的关联。总之,血管化牙龈 CTE 为研究牙周健康和疾病状态下宿主-微生物组相互作用和固有免疫反应提供了一个仿生平台,这为新型牙周治疗药物的开发和评估铺平了道路。