Department of Periodontology, School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Department of Oral and Craniofacial Health Sciences, School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Nat Protoc. 2018 Oct;13(10):2247-2267. doi: 10.1038/s41596-018-0035-4.
Periodontal disease (PD) is a common dental disease associated with the interaction between dysbiotic oral microbiota and host immunity. It is a prevalent disease, resulting in loss of gingival tissue, periodontal ligament, cementum and alveolar bone. PD is a major form of tooth loss in the adult population. Experimental animal models have enabled the study of PD pathogenesis and are used to test new therapeutic approaches for treating the disease. The ligature-induced periodontitis model has several advantages as compared with other models, including rapid disease induction, predictable bone loss and the capacity to study periodontal tissue and alveolar bone regeneration because the model is established within the periodontal apparatus. Although mice are the most convenient and versatile animal models used in research, ligature-induced periodontitis has been more frequently used in large animals. This is mostly due to the technical challenges involved in consistently placing ligatures around murine teeth. To reduce the technical challenge associated with the traditional ligature model, we previously developed a simplified method to easily install a bacterially retentive ligature between two molars for inducing periodontitis. In this protocol, we provide detailed instructions for placement of the ligature and demonstrate how the model can be used to evaluate gingival tissue inflammation and alveolar bone loss over a period of 18 d after ligature placement. This model can also be used on germ-free mice to investigate the role of human oral bacteria in periodontitis in vivo. In conclusion, this protocol enables the mechanistic study of the pathogenesis of periodontitis in vivo.
牙周病(PD)是一种常见的口腔疾病,与失调的口腔微生物群和宿主免疫之间的相互作用有关。它是一种普遍的疾病,会导致牙龈组织、牙周韧带、牙骨质和牙槽骨丧失。PD 是成年人牙齿缺失的主要形式。实验动物模型使 PD 发病机制的研究成为可能,并用于测试治疗该疾病的新治疗方法。与其他模型相比,结扎诱导的牙周炎模型具有几个优点,包括快速疾病诱导、可预测的骨质流失以及研究牙周组织和牙槽骨再生的能力,因为该模型是在牙周装置内建立的。尽管小鼠是研究中最方便和多功能的动物模型,但结扎诱导的牙周炎在大型动物中更为常用。这主要是由于在小鼠牙齿周围始终如一地放置结扎线所涉及的技术挑战。为了减少与传统结扎模型相关的技术挑战,我们之前开发了一种简化方法,可轻松地在两个磨牙之间安装具有细菌保留能力的结扎线以诱导牙周炎。在本方案中,我们提供了放置结扎线的详细说明,并演示了如何在结扎放置后 18 天内使用该模型评估牙龈组织炎症和牙槽骨丧失。该模型也可用于无菌小鼠体内,以研究人类口腔细菌在牙周炎中的作用。总之,本方案使牙周炎发病机制的体内机制研究成为可能。