Enhancement of lipopolysaccharide-stimulated cyclooxygenase-2 mRNA expression and prostaglandin E2 production in gingival fibroblasts from individuals with Down syndrome

被引:17
|
作者
Otsuka, Y
Ito, M
Yamaguchi, M
Saito, S
Uesu, K
Kasai, K
Abiko, Y
Mega, J
机构
[1] Nihon Univ, Sch Dent, Dept Dent Disabled, Chiba 2718587, Japan
[2] Nihon Univ, Sch Dent, Dept Orthodont, Chiba 2718587, Japan
[3] Nihon Univ, Sch Dent, Dept Biochem, Chiba 2718587, Japan
[4] Nihon Univ, Sch Dent, Dept Math, Chiba 2718587, Japan
关键词
Down syndrome; lipopolysaccharide; prostaglandin E-2; periodontal disease; cyclooxygenase-2; real-time PCR;
D O I
10.1016/S0047-6374(01)00413-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It is well known that Down syndrome (DS) is a premature ageing syndrome. Periodontal disease in individuals with DS develops rapidly and extensively in a relatively younger age bracket compared with that in healthy controls. The mechanisms involved in the periodontal inflammatory processes in DS patients are not fully understood. In the present study, the non-inflamed gingival fibroblasts isolated from seven patients with DS (DGF) and seven healthy controls (NDGF) were stimulated with lipopolysaccharide (LPS) derived from Actinobacillus actinomycetemcomitans (A. a.). We measured the level of prostaglandin E-2 (PGE(2)) production by DGF and NDGF by radioimmunoassay, and also measured the mRNA expression of cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) by using the real-time PCR method. We found the higher levels of LPS-stimulated COX-2 mRNA expression and PGE(2) production in DGF when compared with those in NDGF. This study may indicate that overexpression of LPS-stimulated COX-2 induced a greater ability of DGF to produce PGE(2), and that these phenomena may be responsible for the severer periodontal disease in DS patients. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:663 / 674
页数:12
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