Hsieh Hsi-Lung, Sun Chi-Chin, Wu Chou-Bing, Wu Cheng-Ying, Tung Wei-Hsuan, Wang Hui-Hsin, Yang Chuen-Mao
Department of Physiology and Pharmacology, Chang Gung University, Tao-Yuan, Taiwan.
J Cell Biochem. 2008 Apr 15;103(6):1732-46. doi: 10.1002/jcb.21563.
Sphingosine 1-phosphate (S1P) has been shown to regulate expression of several genes in vascular smooth muscle cells (VSMCs) and contributes to arteriosclerosis. However, the mechanisms regulating epidermal growth factor receptor (EGFR) expression by S1P in aortic VSMCs remain unclear. Western blotting and RT-PCR analyses showed that S1P induced EGFR mRNA and protein expression in a time- and concentration-dependent manner, which was attenuated by inhibitors of MEK1/2 (U0126) and phosphatidylinositide 3-kinase (PI3K; wortmannin), and transfection with dominant negative mutants of ERK and Akt, respectively. These results suggested that S1P-induced EGFR expression was mediated through p42/p44 MAPK and PI3K/Akt pathways in VSMCs. In accordance with these findings, S1P stimulated phosphorylation of p42/p44 MAPK and Akt which was attenuated by U0126 and wortmannin, respectively. Furthermore, S1P-induced EGFR upregulation was blocked by a selective NF-kappaB inhibitor helenalin. Immunofluorescent staining and reporter gene assay revealed that S1P-induced activation of NF-kappaB was blocked by wortmannin, but not by U0126, suggesting that activation of NF-kappaB was mediated through PI3K/Akt. Moreover, S1P-induced EGFR expression was inhibited by an AP-1 inhibitor curcumin and tanshinone IIA. S1P-stimulated AP-1 subunits (c-Jun and c-Fos mRNA) expression was attenuated by U0126 and wortmannin, suggesting that MEK and PI3K/ERK cascade linking to AP-1 was involved in EGFR expression. Upregulation of EGFR by S1P may exert a phenotype modulation of VSMCs. This hypothesis was supported by pretreatment with AG1478 or transfection with shRNA of EGFR that attenuated EGF-stimulated proliferation of VSMCs pretreated with S1P, determined by XTT assay. These results demonstrated that in VSMCs, activation of Akt/NF-kappaB and ERK/AP-1 pathways independently regulated S1P-induced EGFR expression in VSMCs. Understanding the mechanisms involved in S1P-induced EGFR expression on VSMCs may provide potential therapeutic targets in the treatment of arteriosclerosis.
1-磷酸鞘氨醇(S1P)已被证明可调节血管平滑肌细胞(VSMC)中多种基因的表达,并参与动脉粥样硬化的形成。然而,S1P在主动脉VSMC中调节表皮生长因子受体(EGFR)表达的机制仍不清楚。蛋白质免疫印迹和逆转录-聚合酶链反应(RT-PCR)分析表明,S1P以时间和浓度依赖性方式诱导EGFR mRNA和蛋白表达,MEK1/2抑制剂(U0126)和磷脂酰肌醇3-激酶(PI3K;渥曼青霉素)以及分别用ERK和Akt的显性负性突变体转染可减弱这种诱导作用。这些结果表明,S1P诱导的EGFR表达是通过VSMC中的p42/p44丝裂原活化蛋白激酶(MAPK)和PI3K/Akt途径介导的。与这些发现一致,S1P刺激p42/p44 MAPK和Akt的磷酸化,而U0126和渥曼青霉素分别减弱了这种磷酸化。此外,S1P诱导的EGFR上调被选择性核因子κB(NF-κB)抑制剂海伦alin阻断。免疫荧光染色和报告基因分析显示,渥曼青霉素可阻断S1P诱导的NF-κB活化,而U0126则不能,这表明NF-κB的活化是通过PI3K/Akt介导的。此外,S1P诱导的EGFR表达被AP-1抑制剂姜黄素和丹参酮IIA抑制。S1P刺激的AP-1亚基(c-Jun和c-Fos mRNA)表达被U0126和渥曼青霉素减弱,这表明与AP-1相关的MEK和PI3K/ERK级联参与了EGFR表达。S1P对EGFR 的上调可能会对VSMC产生表型调节作用。AG1478预处理或用EGFR的短发夹RNA(shRNA)转染可减弱S1P预处理的VSMC中表皮生长因子(EGF)刺激的增殖,这一结果支持了这一假设,该增殖通过XTT法测定。这些结果表明,在VSMC中,Akt/NF-κB和ERK/AP-1途径的激活独立调节S1P诱导的VSMC中EGFR的表达。了解S1P诱导VSMC中EGFR表达的机制可能为动脉粥样硬化的治疗提供潜在的治疗靶点。