Tong Zi-An, Chen Long, Shen Ling, Lu Yi-Fan, Zhang Jian-Wei, Qi Ya-Dong, Qian Yin-Jie, Bao Si-Qi, Chen Wei, Si Mi-Si
Stomatology Hospital, School of Stomatology, Zhejiang University School of Medicine, Zhejiang Provincial Clinical Research Center for Oral Diseases, Key Laboratory of Oral Biomedical Research of Zhejiang Province, Cancer Center of Zhejiang University, Engineering Research Center of Oral Biomaterials and Devices of Zhejiang Province, Hangzhou, Zhejiang, China.
Department of Gastroenterology, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
J Clin Periodontol. 2025 May;52(5):787-798. doi: 10.1111/jcpe.14127. Epub 2025 Jan 16.
To propose a modified method for establishing a peri-implantitis murine model, assess the gene expression profile and immune cell infiltration of the gingiva and alveolar bone, and evaluate the transcriptomic similarity between patients with peri-implantitis and the corresponding murine model.
A ligature-induced peri-implantitis murine model was established using an immediate implant placement approach. RNA sequencing was performed to determine the transcriptomic profiles of peri-implant tissues from mice, patients with peri-implantitis and healthy individuals. Histopathological and bioinformatics analyses were performed to measure immune cell infiltration, bone remodelling, and inflammatory reactions.
Mouse gingival tissue showed strong immune and inflammatory responses, especially macrophage functions; these responses were weaker in the alveolar bone. Humans and mice showed similar gene expression patterns in the gingiva, with greater infiltration of macrophages and neutrophils.
During peri-implantitis progression, mouse gingival tissue exhibited increased immune-related functions and inflammation compared with the alveolar bone. Patients with peri-implantitis and the murine model displayed transcriptomic similarities within the gingiva. We propose that the modified ligature-induced peri-implantitis murine model is suitable for investigating peri-implantitis pathogenesis, with macrophages and neutrophils potentially being critical in its development.
提出一种改良的建立种植体周围炎小鼠模型的方法,评估牙龈和牙槽骨的基因表达谱及免疫细胞浸润情况,并评估种植体周围炎患者与相应小鼠模型之间的转录组相似性。
采用即刻种植植入法建立结扎诱导的种植体周围炎小鼠模型。进行RNA测序以确定来自小鼠、种植体周围炎患者和健康个体的种植体周围组织的转录组谱。进行组织病理学和生物信息学分析以测量免疫细胞浸润、骨重塑和炎症反应。
小鼠牙龈组织表现出强烈的免疫和炎症反应,尤其是巨噬细胞功能;这些反应在牙槽骨中较弱。人类和小鼠在牙龈中表现出相似的基因表达模式,巨噬细胞和中性粒细胞浸润更多。
在种植体周围炎进展过程中,与牙槽骨相比,小鼠牙龈组织表现出免疫相关功能增强和炎症反应。种植体周围炎患者和小鼠模型在牙龈内显示出转录组相似性。我们提出改良的结扎诱导种植体周围炎小鼠模型适用于研究种植体周围炎的发病机制,巨噬细胞和中性粒细胞可能在其发展中起关键作用。