EXPRESSION PATTERNS OF INTERLEUKIN-6 AND MICRORNA-146A DURING ORTHODONTIC RELAPSE IN A RAT MODEL

被引:0
作者
Dai, J. -Y. [1 ]
Li, S. -Q. [1 ]
Jia, X. [2 ]
Wu, M. -Y. [1 ]
Song, B. [1 ]
Li, J. -Y. [1 ]
Guo, Y. [1 ]
Gao, R. [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Orthodont, 143 Yiman St, Harbin 150001, Peoples R China
[2] Harbin Stomatol Hosp, Dept Orthodont, Harbin 150001, Peoples R China
来源
JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY | 2024年 / 75卷 / 04期
关键词
orthodontic relapse; interleukin-6; microR-146a; orthodontic tooth movement model; periodontal tissue; gingival crevicular fluid; human premolar tooth tissue; GINGIVAL CREVICULAR FLUID; NECROSIS-FACTOR-ALPHA; TOOTH MOVEMENT; PERIODONTAL-LIGAMENT;
D O I
10.26402/jpp.2024.4.10
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
In this study, we established an experimental rat model to simulate orthodontic tooth movement relapse and a human periodontal ligament stem cell (PDLScs) model. Our aim was to explore the relationship between microRNA-146a (miR-146a) expression in periodontal tissue, the inflammatory factor interleukin-6 (IL-6), and orthodontic relapse subsequent to mechanical intervention. In the animal experiment, a total of 30 healthy male Wistar rats were randomly allocated to either the control group (n=6) or the model group (n=24). In the model group, the orthodontic appliance was removed 14 days after force application. Gingival crevicular fluid (GcF) and periodontal tissue samples were collected at intervals of days 0, 7, 14, and 21 following removal of the orthodontic appliance to assess alterations in miR-146a and IL-6 expressions. In the in vitro cell culture study, human premolar tooth tissue was isolated 24 hours following the addition of the transfection reagent to harvest PDLScs. Reverse transcription quantitative polymerase chain reaction was employed to evaluate the expression levels of the miRNA-146a gene, while Western blot analysis was utilized to assess the production of the IL-6 protein. As a result in comparison to the control group, the protein expression of IL-6 notably escalated to its peak value in the model-day 7 group (p<0.05). Subsequently, although experiencing a slight decline, the IL-6 expression in the model-day 14 group remained significantly elevated compared to control group (p<0.05). In the model-day 21 group, the protein expression of IL-6 approached that of the control group, with no significant difference observed (p>0.05). conversely, in relation to the control group, the gene expression of miR-146a drastically decreased to its lowest point in the model-day 7 group (p<0.05). While exhibiting a slight increase, the miR-146a expression in the model-day 14 group remained significantly diminished compared to control group (p<0.05). Following the identification of human periodontal ligament cells (hPDLcs) through immunofluorescence in the in vitro study, a subsequent experiment was conducted to specifically inhibit miR-146a expression. In comparison to the control group, the protein expression of IL-6 demonstrated a significant increase in the anti-miRNA oligodeoxyribonucleotide (AMO) group, where miR-146a expression was effectively suppressed (p<0.05). Throughout the process of orthodontic tooth movement relapse in rats, there was a notable reduction in the gene expression of miR-146a, accompanied by a significant increase in the expression of IL-6.
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收藏
页码:447 / 456
页数:10
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