Cheng Xin-Yi, Zou Pei-Hui, Ma Yi-Ming, Cai Yu, Shi Qiao, Liu Jia, Luan Qing-Xian
Department of Periodontology, Peking University School and Hospital of Stomatology & National Center for Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices& Beijing Key Laboratory of Digital Stomatology & NHC Key Laboratory of Digital Stomatology & NMPA Key Laboratory for Dental Materials, Beijing, China.
J Dent Sci. 2025 Jan;20(1):292-301. doi: 10.1016/j.jds.2024.07.009. Epub 2024 Jul 20.
BACKGROUND/PURPOSE: Periodontitis is associated with systemic health. One of the underlying mechanisms is the translocation of periodontal pathogens, among which () is the most common. Here, we aimed to illustrate the biodistribution and dynamics of from gingiva to multiple organs through blood circulation.
tagged by Cyanine 7 (Cy7-) was injected into the gingiva of healthy and periodontitis mice. imaging system (IVIS) was applied to monitor the distribution of Cy7- in multiple organs which were isolated at serial timepoints. Polymerase chain reaction (PCR) was conducted to determine the DNA copies in the gingiva, blood and organs. Cy7- in the gingiva and organs was also confirmed by frozen section staining. Furthermore, to figure out whether the bacteremia derived from oral-gut axis, mice received gavage of Cy7-. Then the blood and organ samples were detected in the similar way as above.
Intra-gingival injection induced larger amounts of Cy7- accumulating in the gingiva of periodontitis mice ( 0.05) as confirmed by above three methods. Twenty minutes after injection, DNA copies in the blood of periodontitis group were 36.3-fold higher than healthy group ( 0.05). IVIS results, combined with PCR and frozen sections, demonstrated periodontitis induced longer retention with higher amounts of Cy7- in the periodontitis group. was enriched more significantly in the liver for the longer duration than the kidney and pancreas.
Our study showed , which accumulated in the gingiva, could translocate through blood circulation to multiple organs with varied duration and amounts.
背景/目的:牙周炎与全身健康相关。潜在机制之一是牙周病原体的易位,其中(某病原体,原文未明确写出)最为常见。在此,我们旨在阐明(该病原体)从牙龈经血液循环至多个器官的生物分布及动态变化。
将用菁氰7(Cy7 -)标记的(该病原体)注射到健康和牙周炎小鼠的牙龈中。应用成像系统(IVIS)监测在连续时间点分离的多个器官中Cy7 -的分布。进行聚合酶链反应(PCR)以确定牙龈、血液和器官中的(该病原体)DNA拷贝数。牙龈和器官中的Cy7 -也通过冰冻切片染色得以证实。此外,为弄清楚菌血症是否源自口腔 - 肠道轴,给小鼠灌胃Cy7 -标记的(该病原体)。然后以与上述类似的方式检测血液和器官样本。
牙龈内注射导致更多的Cy7 -在牙周炎小鼠的牙龈中蓄积(P < 0.05),上述三种方法均证实了这一点。注射后20分钟,牙周炎组血液中的(该病原体)DNA拷贝数比健康组高36.3倍(P < 0.05)。IVIS结果,结合PCR和冰冻切片,表明牙周炎导致牙周炎组中Cy7 -的滞留时间更长且量更多。与肾脏和胰腺相比,(该病原体)在肝脏中富集更显著且持续时间更长。
我们的研究表明,蓄积在牙龈中的(该病原体)可经血液循环转移至多个器官,且转移的持续时间和量各不相同。