University of Leicester Department of Cardiovascular Science and Department of Molecular and Cell Biology, Henry Wellcome Building, Lancaster Road, Leicester, LE1 7RH, UK.
University of Warwick, Department of Engineering, School of Engineering, Coventry, CV4 7AL, UK.
Sci Rep. 2017 Jun 16;7(1):3658. doi: 10.1038/s41598-017-03981-6.
Angiopoietin-1 (Angpt1) is a glycoprotein ligand important for maintaining the vascular system. It signals via a receptor tyrosine kinase expressed on the surface on endothelial cells, Tie2. This receptor can undergo regulated ectodomain cleavage that releases the ligand-binding domain (sTie2) into the circulation. The concentration of sTie2 is increased in a range of conditions, including peripheral arterial disease and myocardial infarction, where it has been suggested to bind and block Angpt1 resulting in vascular dysfunction. Here we use a joint mathematical modelling and experimental approach to assess the potential impact of sTie2 on the ability of Angpt1 to signal. We find that the concentrations of sTie2 relative to Angpt1 required to suppress signalling by the ligand are more than ten-fold higher than those ever seen in normal or disease conditions. In contrast to the endogenous sTie2, an engineered form of sTie2, which presents dimeric ligand binding sites, inhibits Angpt1 signalling at seventy-fold lower concentrations. While loss of Tie2 ectodomain can suppress Angpt1 signalling locally in the cells in which the receptor is lost, our study shows that the resulting increase in circulating sTie2 is unlikely to affect Angpt1 activity elsewhere in the body.
血管生成素-1(Angpt1)是一种糖蛋白配体,对于维持血管系统非常重要。它通过在血管内皮细胞表面表达的受体酪氨酸激酶 Tie2 发出信号。该受体可以进行调节性细胞外结构域裂解,将配体结合结构域(sTie2)释放到循环中。sTie2 的浓度在多种情况下增加,包括外周动脉疾病和心肌梗死,其中有人提出它可以结合并阻断 Angpt1,从而导致血管功能障碍。在这里,我们使用联合数学建模和实验方法来评估 sTie2 对 Angpt1 信号传递能力的潜在影响。我们发现,相对于 Angpt1 抑制配体信号所需的 sTie2 浓度,是正常或疾病条件下从未见过的浓度的十倍以上。与内源性 sTie2 相反,一种呈现二聚体配体结合位点的工程化形式的 sTie2,以低至 70 倍的浓度抑制 Angpt1 信号。虽然 Tie2 细胞外结构域的缺失可以局部抑制受体丧失的细胞中 Angpt1 的信号,但我们的研究表明,循环中 sTie2 的增加不太可能影响体内其他部位的 Angpt1 活性。