CORM-3 Inhibits the Inflammatory Response of Human Periodontal Ligament Fibroblasts Stimulated by LPS and High Glucose

被引:1
|
作者
Tian, Haoyang [1 ,2 ,3 ,4 ]
Chen, Hui [5 ]
Yin, Xiaochun [5 ]
Lv, Meiyi [6 ]
Wei, Lingling [1 ,2 ,3 ,4 ]
Zhang, Yuna [7 ]
Jia, Shuhan [8 ]
Li, Jingyuan [1 ,2 ,3 ,4 ]
Song, Hui [1 ,2 ,3 ,4 ]
机构
[1] Shandong Univ, Sch & Hosp Stomatol, Cheeloo Coll Med, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[2] Shandong Key Lab Oral Tissue Regenerat, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[3] Shandong Engn Lab Dent Mat & Oral Tissue Regenerat, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[4] Shandong Prov Clin Res Ctr Oral Dis, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[5] Jinan Stomatol Hosp, Dept Endodont, Jinan, Peoples R China
[6] Jinan Stomatol Hosp, Dept Pediat Dent, Jinan, Peoples R China
[7] Guangxi Med Univ, Affiliated Hosp 1, Dept Stomatol, Nanning, Peoples R China
[8] Yancheng NO 1 Peoples Hosp, Dept Stomatol, Yancheng, Peoples R China
关键词
carbon monoxide-releasing molecules; periodontitis; diabetes; receptor for advanced glycation end products; lipopolysaccharide; MONOXIDE-RELEASING MOLECULE; TYPE-2; DIABETES-MELLITUS; GLYCATION END-PRODUCTS; CARBON-MONOXIDE; GLYCEMIC CONTROL; CO-RMS; CELLS; APOPTOSIS; THERAPY; ACTIVATION;
D O I
10.2147/JIR.S460954
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Diabetes has been recognized as an independent risk factor for periodontitis. Increasing evidences indicate that hyperglycemia aggravates inflammatory response of human periodontal ligament cells (hPDLCs). Carbon monoxide-releasing molecule-3 (CORM-3) is a water-soluble compound that can release carbon monoxide (CO) in a controllable manner. CORM-3 has been shown the anti-inflammatory effect in different cell lineages. Methods: We stimulated periodontal ligament cells with LPS and high glucose. The expression of inflammatory cytokine was detected by ELISA. RT-qPCR, Western blot and immunofluorescence were used to detect the expression of TLR2, TLR4, RAGE and the activation of NF-kappa B pathway. We performed silencing and overexpression treatment of RAGE targeting the role of RAGE. We performed the immunostaining of paraffin sections of the periodontitis model in diabetes rats. Results: The results showed that CORM-3 significantly inhibited the expression of inflammatory cytokine in hPDLCs stimulated with LPS and high glucose. CORM-3 also inhibited LPS and high glucose-induced expression of RAGE/NF-kappa B pathway and TLR2/TLR4/ NF-kappa B pathway. Silence of RAGE resulted in significantly decreased expression of proteins above. Overexpression of RAGE significantly enhanced the expression of these factors. CORM-3 abrogated the effect of RAGE partially. In animal model, CORM-3 suppressed the inflammatory response of periodontal tissues in experimental periodontitis of diabetic rats. Discussion: Our research proved CORM-3 reduced the inflammatory response via RAGE/NF-kappa B pathway and TLR2/TLR4/NF-kappa B pathway in the process of high glucose exacerbated periodontitis. These findings demonstrated the role of RAGE in the process of high glucose exacerbated periodontitis and suggested that CORM3 be a potential therapeutic strategy for the treatment of diabetes patients with periodontitis.
引用
收藏
页码:4845 / 4863
页数:19
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