Fuentes Lida Q, Reyes Carlos E, Sarmiento José M, Villanueva Carolina I, Figueroa Carlos D, Navarro Javier, González Carlos B
Department of Physiology, Universidad Austral de Chile, Valdivia, Chile.
Cell Signal. 2008 Sep;20(9):1642-50. doi: 10.1016/j.cellsig.2008.05.009. Epub 2008 May 25.
Activation of V(1a) receptor triggers the expression of growth-related immediate-early genes (IEGs), including c-Fos and Egr-1. We found that pre-treatment of rat vascular smooth muscle A-10 cell line with the EGF receptor inhibitor AG1478 or the over-expression of an EGFR dominant negative mutant (HEBCD533) blocked the vasopressin-induced expression of IEGs, suggesting that activation of these early genes mediated by V(1a) receptor is via transactivation of the EGF receptor. Importantly, the inhibition of the metalloproteinases, which catalyzed the shedding of the EGF receptor agonist HB-EGF, selectively blocked the vasopressin-induced expression c-Fos. On the other hand, the inhibition of c-Src selectively blocked the vasopressin-induced expression of Egr-1. Interestingly, in contrast to the expression of c-Fos, the expression of Egr-1 was mediated via the Ras/MEK/MAPK-dependent signalling pathway. Vasopressin-triggered expression of both genes required the release of intracellular calcium, activation of PKC and beta-arrestin 2. These findings demonstrated that vasopressin up-regulated the expression of c-Fos and Erg-1 via transactivation of two distinct EGF receptor-dependent signalling pathways.
V(1a)受体的激活会触发与生长相关的即刻早期基因(IEGs)的表达,包括c-Fos和Egr-1。我们发现,用表皮生长因子(EGF)受体抑制剂AG1478预处理大鼠血管平滑肌A-10细胞系,或过表达EGFR显性负性突变体(HEBCD533),均可阻断血管加压素诱导的IEGs表达,这表明由V(1a)受体介导的这些早期基因的激活是通过EGF受体的反式激活实现的。重要的是,抑制催化EGF受体激动剂HB-EGF脱落的金属蛋白酶,可选择性地阻断血管加压素诱导的c-Fos表达。另一方面,抑制c-Src可选择性地阻断血管加压素诱导的Egr-1表达。有趣的是,与c-Fos的表达不同,Egr-1的表达是通过Ras/MEK/MAPK依赖性信号通路介导的。血管加压素触发的这两个基因的表达都需要细胞内钙的释放、蛋白激酶C(PKC)和β-抑制蛋白2的激活。这些发现表明,血管加压素通过两条不同的EGF受体依赖性信号通路的反式激活上调了c-Fos和Erg-1的表达。