Lee Nam Y, Blobe Gerard C
Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA.
J Biol Chem. 2007 Jul 20;282(29):21507-17. doi: 10.1074/jbc.M700176200. Epub 2007 May 31.
In endothelial cells, transforming growth factor beta (TGF-beta) signals through two distinct pathways to regulate endothelial cell proliferation and migration, the ALK-1/Smads 1/5/8 pathway and the ALK-5/Smads 2/3 pathway. TGF-beta signaling through these pathways is further regulated in endothelial cells by the endothelial specific TGF-beta superfamily co-receptor, endoglin. The importance of endoglin, ALK-1, and ALK-5 in endothelial biology is underscored by the embryonic lethal phenotypes of knock-outs in mice due to defects in angiogenesis, and by the presence of disease-causing mutations in these genes in human vascular diseases. However, the mechanism of action of endoglin is not well defined. Here we define a novel interaction between endoglin and the scaffolding protein beta-arrestin2. Both co-immunoprecipitation and fluorescence confocal studies demonstrate the specific interaction between endoglin and beta-arrestin2 in endothelial cells, enhanced by ALK-1 and to a lesser extent by the type II TGF-beta receptor. The endoglin/beta-arrestin2 interaction results in endoglin internalization and co-accumulation of endoglin and beta-arrestin2 in endocytic vesicles. Whereas endoglin did not have a direct impact on either Smad 2/3 or Smad 1/5/8 activation, endoglin antagonized TGF-beta-mediated ERK signaling, altered the subcellular distribution of activated ERK, and inhibited endothelial cell migration in a manner dependent on the ability of endoglin to interact with beta-arrestin2. Reciprocally, small interfering RNA-mediated silencing of endogenous beta-arrestin2 expression restored TGF-beta-mediated ERK activation and increased endothelial cell migration in an endoglin-dependent manner. These studies define a novel function for endoglin, and further expand the roles mediated by the ubiquitous scaffolding protein beta-arrestin2.
在内皮细胞中,转化生长因子β(TGF-β)通过两条不同的途径发出信号,以调节内皮细胞的增殖和迁移,即ALK-1/Smads 1/5/8途径和ALK-5/Smads 2/3途径。在内皮细胞中,内皮特异性TGF-β超家族共受体内皮糖蛋白进一步调节通过这些途径的TGF-β信号传导。由于血管生成缺陷,小鼠敲除后的胚胎致死表型以及人类血管疾病中这些基因中致病突变的存在,突显了内皮糖蛋白、ALK-1和ALK-5在内皮生物学中的重要性。然而,内皮糖蛋白的作用机制尚未明确。在此,我们定义了内皮糖蛋白与支架蛋白β-抑制蛋白2之间的一种新型相互作用。共免疫沉淀和荧光共聚焦研究均证明了内皮糖蛋白与β-抑制蛋白2在内皮细胞中的特异性相互作用,这种相互作用被ALK-1增强,而被II型TGF-β受体在较小程度上增强。内皮糖蛋白/β-抑制蛋白2相互作用导致内皮糖蛋白内化以及内皮糖蛋白和β-抑制蛋白2在内吞小泡中共积累。虽然内皮糖蛋白对Smad 2/3或Smad 1/5/8的激活没有直接影响,但内皮糖蛋白拮抗TGF-β介导的ERK信号传导,改变了活化ERK的亚细胞分布,并以依赖于内皮糖蛋白与β-抑制蛋白2相互作用能力的方式抑制内皮细胞迁移。相反,小干扰RNA介导的内源性β-抑制蛋白2表达沉默恢复了TGF-β介导的ERK激活,并以内皮糖蛋白依赖的方式增加了内皮细胞迁移。这些研究定义了内皮糖蛋白的一种新功能,并进一步扩展了普遍存在的支架蛋白β-抑制蛋白2所介导的作用。