Phosphatidic acid as a regulator of matrix metalloproteinase-9 expression via the TNF-α signaling pathway

被引:27
|
作者
Lee, Jin-Gu
Lee, Sun-Hye
Park, Dae-Weon
Bae, Yoe-Sik
Yun, Sung-Su
Kim, Jae-Ryong
Baek, Suk-Hwan [1 ]
机构
[1] Yeungnam Univ, Dept Biochem & Mol Biol, Aging Assoc Vasc Dis Res Ctr, Taegu 705717, South Korea
[2] Dong A Univ, Coll Med, Dept Biochem, Pusan, South Korea
[3] Yeungnam Univ, Coll Med, Dept Surg, Taegu 705717, South Korea
基金
新加坡国家研究基金会;
关键词
phosphatidic acid; tumor necrosis factor-alpha; TNF receptor; matrix metalloproteinase-9;
D O I
10.1016/j.febslet.2007.01.048
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
Phosphatidic acid (PA) is implicated in pathophysiological processes associated with cellular signaling events and inflammation, which include the expressional regulation of numerous genes. Here, we show that PA stimulation increases matrix metalloproteinase-9 (MMP-9) expression in macrophages through tumor necrosis factor (TNF)-alpha signaling. We performed antibody array analysis on proteins from macrophages stimulated with PA. PA was found to induce the production of TNF-alpha, but not of TNF receptor (TNFR)1 and TNFR2 in a time-dependent manner and stimulated significant, though delayed, MMP-9 expression. PA induced the phosphorylations of both ERK1/2 and p38, but not of c-jun amino-terminal kinase. Moreover, only ERK1/2 inhibition by U0126 suppressed PA-induced TNF-a production and MMP-9 expression. Neutralizing TNF-alpha, TNFR1 or TNFR2 antibodies significantly suppressed PA-induced MMP-9 expression, suggesting that the production of TNF-a in response to PA preceded the expression of MMP-9. Moreover, lipopolysaccharide-induced PA also led to TNF-alpha release and resulted in MMP-9 expression. Taken together, these observations suggest that PA may play a role in MMP-9 regulation through ERKs/TNF-alpha/TNFRs-dependent signaling pathway. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:787 / 793
页数:7
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