Lebrin Franck, Deckers Martine, Bertolino Philippe, Ten Dijke Peter
Division of Cellular Biochemistry, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
Cardiovasc Res. 2005 Feb 15;65(3):599-608. doi: 10.1016/j.cardiores.2004.10.036.
Genetic studies in mice and humans have revealed the pivotal role of transforming growth factor-beta (TGF-beta) signaling during angiogenesis. Mice deficient for various TGF-beta signaling components present an embryonic lethality due to vascular defects. In patients, mutations in the TGF-beta type I receptor ALK1 or in the accessory TGF-beta receptor endoglin are linked to an autosomal dominant disorder of vascular dysplasia termed Hereditary Haemorrhagic Telangiectasia (HHT). It has puzzled researchers for years to explain the effects of TGF-beta being a stimulator and an inhibitor of angiogenesis in vitro and in vivo. Recently, a model has been proposed in which TGF-beta by binding to the TGF-beta type II receptor can activate two distinct type I receptors in endothelial cells (ECs), i.e., the EC-restricted ALK1 and the broadly expressed ALK-5, which have opposite effects on ECs behavior. ALK1 via Smad1/5 transcription factors stimulates EC proliferation and migration, whereas ALK5 via Smad2/3 inhibits EC proliferation and migration. Here, the new findings are presented concerning the molecular mechanisms that take place in ECs to precisely regulate and even switch between TGF-beta-induced biological responses. In particular, the role of the accessory TGF-beta receptor endoglin in the regulation of EC behavior is addressed and new insights are discussed concerning the possible mechanisms that are implicated in the development of HHT.
对小鼠和人类的遗传学研究揭示了转化生长因子-β(TGF-β)信号传导在血管生成过程中的关键作用。缺乏各种TGF-β信号传导成分的小鼠由于血管缺陷而出现胚胎致死性。在患者中,TGF-β I型受体ALK1或辅助性TGF-β受体内皮糖蛋白的突变与一种称为遗传性出血性毛细血管扩张症(HHT)的常染色体显性血管发育异常疾病有关。多年来,研究人员一直困惑于如何解释TGF-β在体外和体内既是血管生成的刺激剂又是抑制剂的作用。最近,有人提出了一个模型,其中TGF-β通过与TGF-β II型受体结合,可以激活内皮细胞(ECs)中的两种不同的I型受体,即ECs特异性的ALK1和广泛表达的ALK-5,它们对ECs行为具有相反的影响。ALK1通过Smad1/5转录因子刺激ECs增殖和迁移,而ALK5通过Smad2/3抑制ECs增殖和迁移。在此,本文介绍了有关ECs中发生的精确调节甚至在TGF-β诱导的生物学反应之间切换的分子机制的新发现。特别是,探讨了辅助性TGF-β受体内皮糖蛋白在调节ECs行为中的作用,并讨论了与HHT发生发展可能相关的机制的新见解。