Nemoto Takahiro, Kubota Shunichiro
Department of Physiological Chemistry and Metabolism, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Tokyo 113-0033, Japan.
Cell Biol Int. 2007 Feb;31(2):141-7. doi: 10.1016/j.cellbi.2006.09.019. Epub 2006 Sep 28.
In the present study, we investigated the relationship between ornithine decarboxylase, MAP kinase, and MMP-2 expression in vitro. Overexpression of ornithine decarboxylase cDNA induced MMP-2 expression both at mRNA and protein levels. Promoter analysis and gel shift assay showed that p53 and Ets-1 were involved in MMP-2 expression in ornithine decarboxylase overexpressing transfectants. Erk and p38 MAP kinase were significantly activated. Using specific inhibitors of MEK and p38, we clarified that MMP-2 expression was induced via both Erk and p38 MAP kinase signaling pathways. This is the first report showing the existence of a causal relationship between ornithine decarboxylase expression, Erk and p38 MAP kinase activation, and MMP-2 expression.
在本研究中,我们在体外研究了鸟氨酸脱羧酶、丝裂原活化蛋白激酶(MAP激酶)和基质金属蛋白酶-2(MMP-2)表达之间的关系。鸟氨酸脱羧酶cDNA的过表达在mRNA和蛋白质水平均诱导了MMP-2的表达。启动子分析和凝胶迁移试验表明,p53和Ets-1参与了过表达鸟氨酸脱羧酶的转染细胞中MMP-2的表达。细胞外信号调节激酶(Erk)和p38 MAP激酶被显著激活。使用MEK和p38的特异性抑制剂,我们阐明MMP-2的表达是通过Erk和p38 MAP激酶信号通路诱导的。这是首份表明鸟氨酸脱羧酶表达、Erk和p38 MAP激酶激活与MMP-2表达之间存在因果关系的报告。