Goumans Marie José, Valdimarsdottir Gudrun, Itoh Susumu, Lebrin Franck, Larsson Jonas, Mummery Christine, Karlsson Stefan, ten Dijke Peter
Division of Cellular Biochemistry, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands.
Mol Cell. 2003 Oct;12(4):817-28. doi: 10.1016/s1097-2765(03)00386-1.
Transforming growth factor-beta (TGFbeta) regulates the activation state of the endothelium via two opposing type I receptor/Smad pathways. Activin receptor-like kinase-1 (ALK1) induces Smad1/5 phosphorylation, leading to an increase in endothelial cell proliferation and migration, while ALK5 promotes Smad2/3 activation and inhibits both processes. Here, we report that ALK5 is important for TGFbeta/ALK1 signaling; endothelial cells lacking ALK5 are deficient in TGFbeta/ALK1-induced responses. More specifically, we show that ALK5 mediates a TGFbeta-dependent recruitment of ALK1 into a TGFbeta receptor complex and that the ALK5 kinase activity is required for optimal ALK1 activation. TGFbeta type II receptor is also required for ALK1 activation by TGFbeta. Interestingly, ALK1 not only induces a biological response opposite to that of ALK5 but also directly antagonizes ALK5/Smad signaling.
转化生长因子-β(TGFβ)通过两条相反的I型受体/Smad信号通路调节内皮细胞的激活状态。激活素受体样激酶-1(ALK1)诱导Smad1/5磷酸化,导致内皮细胞增殖和迁移增加,而ALK5促进Smad2/3激活并抑制这两个过程。在此,我们报道ALK5对TGFβ/ALK1信号传导很重要;缺乏ALK5的内皮细胞在TGFβ/ALK1诱导的反应中存在缺陷。更具体地说,我们表明ALK5介导TGFβ依赖性地将ALK1募集到TGFβ受体复合物中,并且ALK5激酶活性是最佳激活ALK1所必需的。TGFβ II型受体对于TGFβ激活ALK1也是必需的。有趣的是,ALK1不仅诱导与ALK5相反的生物学反应,而且还直接拮抗ALK5/Smad信号传导。