Fu Mingui, Zhang Jifeng, Lin Yimin, Zhu Xiaojun, Zhao Luning, Ahmad Mushtaq, Ehrengruber Markus U, Chen Yuqing E
Cardiovascular Research Institute, Morehouse School of Medicine, 720 Westview Drive SW, Atlanta, GA 30310, USA.
Biochem J. 2003 Mar 15;370(Pt 3):1019-25. doi: 10.1042/BJ20021503.
Transforming growth factor beta (TGF beta) and peroxisome proliferator-activated receptor gamma (PPAR gamma) play major roles in the development of vascular diseases. It has been documented that PPAR gamma activation inhibits the TGF beta signal pathway in vascular smooth muscle cells (VSMC). Here we examined whether TGF beta can regulate PPAR gamma expression. Northern blot analyses revealed that both TGF beta 1 and 2 exert a biphasic effect (early stimulation and late repression) on PPAR gamma gene expression in VSMC. TGF beta rapidly and transiently induced early growth-response factor-1 (Egr-1) expression through the mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1 (MEK1)/ERK-mediated pathway. Inhibition of MEK1/ERK by PD98059 not only abrogated the induction of Egr-1 but also abolished the rapid and transient induction of PPAR gamma by TGF beta. Furthermore, overexpression of NAB2, a repressor of Egr-1 activation, also blocked the induction of PPAR gamma by TGF beta in VSMC, suggesting that Egr-1 mediates the rapid and transient induction of PPAR gamma by TGF beta. With regard to the TGF beta repression of PPAR gamma expression, activator protein 1 (AP1) and Smad3/4 dramatically inhibited the PPAR gamma promoter activity in transient-transfection studies. In contrast, adenovirus-mediated overexpression of a dominant-negative form of c-Jun partially rescued the TGF beta-induced PPAR gamma repression in VSMC. Taken together, our data demonstrate that Egr-1, AP1 and Smad are part components of the TGF beta signal transduction pathway that regulates PPAR gamma expression.
转化生长因子β(TGFβ)和过氧化物酶体增殖物激活受体γ(PPARγ)在血管疾病的发展中起主要作用。已有文献记载,PPARγ激活可抑制血管平滑肌细胞(VSMC)中的TGFβ信号通路。在此,我们研究了TGFβ是否能调节PPARγ的表达。Northern印迹分析显示,TGFβ1和2对VSMC中PPARγ基因表达均有双相作用(早期刺激和晚期抑制)。TGFβ通过丝裂原活化蛋白激酶/细胞外信号调节激酶激酶1(MEK1)/ERK介导的途径快速且短暂地诱导早期生长反应因子-1(Egr-1)表达。用PD98059抑制MEK1/ERK不仅消除了Egr-1的诱导,也消除了TGFβ对PPARγ的快速且短暂的诱导。此外,Egr-1激活的抑制剂NAB2的过表达也阻断了TGFβ在VSMC中对PPARγ的诱导,表明Egr-1介导了TGFβ对PPARγ的快速且短暂的诱导。关于TGFβ对PPARγ表达的抑制,在瞬时转染研究中,活化蛋白1(AP1)和Smad3/4显著抑制了PPARγ启动子活性。相反,腺病毒介导的显性负性形式的c-Jun过表达部分挽救了TGFβ诱导的VSMC中PPARγ的抑制。综上所述,我们的数据表明,Egr-1、AP1和Smad是调节PPARγ表达的TGFβ信号转导途径的部分组成成分。