Oxidized low-density lipoprotein-induced periodontal inflammation is associated with the up-regulation of cyclooxygenase-2 and microsomal prostaglandin synthase 1 in human gingival epithelial cells

被引:22
作者
Nagahama, Yu [2 ]
Obama, Takashi
Usui, Michihiko [2 ]
Kanazawa, Yukari
Iwamoto, Sanju [3 ]
Suzuki, Kazushige [2 ]
Miyazaki, Akira [3 ]
Yamaguchi, Tomohiro
Yamamoto, Matsuo [2 ]
Itabe, Hiroyuki [1 ]
机构
[1] Showa Univ, Sch Pharm, Dept Biol Chem, Shinagawa Ku, Tokyo 1428555, Japan
[2] Showa Univ, Dent Hosp, Sch Dent, Dept Periodontol, Tokyo 1428555, Japan
[3] Showa Univ, Sch Med, Dept Biochem, Tokyo 1428555, Japan
关键词
Periodontitis; Oxidized low-density lipoprotein; Interleukin-8; Human gingival epithelial cells; Cyclooxygenase-2; FACTOR-KAPPA-B; GENE-EXPRESSION; DISEASE; LIPOPOLYSACCHARIDE; INTERLEUKIN-1-BETA; MACROPHAGES; PARAMETERS; PROTEIN-1; ALPHA; LDL;
D O I
10.1016/j.bbrc.2011.09.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Periodontitis is characterized by chronic gingival tissue inflammation, and inflammatory mediators such as IL-8 and prostaglandin E-2 (PGE(2)) are associated with disease progression. Previously we showed that oxidatively modified low-density lipoprotein (oxLDL) was present in gingival crevicular fluid. In this study, the role of oxLDL in the gingival epithelial cell inflammatory response was further investigated using Ca9-22 cells and primary human oral keratinocytes (HOK). Treatment of Ca9-22 cells and HOK with oxLDL induced an up-regulation of IL-8 and the PGE(2)-producing enzymes, cyclooxygenase-2 and microsomal PGE(2) synthase-1. These responses induced by oxLDL were significantly suppressed by a nuclear factor-kappa B (NF-kappa B) inhibitor. However, unlike the result in macrophages, oxLDL did not lead to an increase in CD36 expression in these two cells. These results suggest that oxLDL elicits gingival epithelial cell inflammatory responses through an activation of the NF-kappa B pathway. These data suggest a mechanistic link between periodontal disease and lipid metabolism-related disorders, including atherosclerosis. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:566 / 571
页数:6
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