Signal pathway involved in inhibition by lipoxin A4 of production of interleukins induced in endothelial cells by lipopolysaccharide

被引:69
作者
Wu, S. -H. [1 ]
Liao, P. -Y. [1 ]
Dong, L. [1 ]
Chen, Z. -Q. [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Pediat, Cent Lab, Jiangsu 210029, Jiangsu, Peoples R China
关键词
lipoxin; lipopolysaccharide; interleukin; nuclear factor-kappa B; endothelial cells;
D O I
10.1007/s00011-008-7147-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective and design: We examine whether lipoxin A(4) (LXA(4)) inhibits production of interleukins (ILs) in endothelial cells and what signal pathway might participate in the actions of LXA(4). Methods: Cultured pulmonary microvascular endothelial cells (PMVEC) were treated with lipopolysaccharide (LPS), with or without preincubation with LXA(4). Results: The results showed that LPS induced production of IL-I beta, IL-6 and IL-8 in rat PMVEC, upregulated the expressions of myeloid differentiation factor 88 (MyD88), phosphorylated p38 and p42/44 mitogen-activated protein kinase (MAPK), phosphorylated phosphoinositide 3-kinase (PI3-K), DNA-binding activities of nuclear factor-kappa B (NF-kappa B) and activator protein-1 (AP-1). The blockade of p38 MAPK, p42/44 MAPK, PI3-K, NF-kappa B or AP-1 partially inhibited production of IL-1 beta, IL-6 and IL-8 stimulated by LPS, respectively. LXA4 significantly inhibited LPS-stimulated secretion of protein and expressions of mRNA of IL-1 beta, IL-6 and IL-8, activation of p38 MAPK, p42/44 MAPK, PI3-K, NF-kappa B and AP-1 but not MyD88 in PMVEC. Conclusions: LXA4 inhibits synthesis of IL-1 beta, IL-6 and IL-8 in PMVEC and this antagonism is related to PI3-K, p38 and p42/44 MAPK, NF-kappa B and AP-1 pathway-dependent signal transduction.
引用
收藏
页码:430 / 437
页数:8
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