From the Division of Developmental Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD (S.K., A.N.S., C.H.M., J.G., D.C., B.M.W.); Departments of Biochemistry and Cell Biology and of Pathology, Geisel School of Medicine at Dartmouth College, Lebanon, NH (R.V.S.); Vascular Biology Program, IFOM, FIRC Institute of Molecular Oncology Foundation, Milan, Italy (M.M., E.D.); and Department of Immunology, Genetics and Pathology, Uppsala University, Sweden (E.D.).
Arterioscler Thromb Vasc Biol. 2018 Feb;38(2):353-362. doi: 10.1161/ATVBAHA.117.309571. Epub 2017 Dec 28.
The assembly of a functional vascular system requires a coordinated and dynamic transition from activation to maturation. High vascular endothelial growth factor activity promotes activation, including junction destabilization and cell motility. Maturation involves junctional stabilization and formation of a functional endothelial barrier. The identity and mechanism of action of prostabilization signals are still mostly unknown. Bone morphogenetic protein receptors and their ligands have important functions during embryonic vessel assembly and maturation. Previous work has suggested a role for growth differentiation factor 6 (GDF6; bone morphogenetic protein 13) in vascular integrity although GDF6's mechanism of action was not clear. Therefore, we sought to further explore the requirement for GDF6 in vascular stabilization.
We investigated the role of GDF6 in promoting endothelial vascular integrity in vivo in zebrafish and in cultured human umbilical vein endothelial cells in vitro. We report that GDF6 promotes vascular integrity by counteracting vascular endothelial growth factor activity. GDF6-deficient endothelium has increased vascular endothelial growth factor signaling, increased vascular endothelial-cadherin Y658 phosphorylation, vascular endothelial-cadherin delocalization from cell-cell interfaces, and weakened endothelial cell adherence junctions that become prone to vascular leak.
Our results suggest that GDF6 promotes vascular stabilization by restraining vascular endothelial growth factor signaling. Understanding how GDF6 affects vascular integrity may help to provide insights into hemorrhage and associated vascular pathologies in humans.
功能性血管系统的构建需要从激活到成熟的协调和动态转变。高血管内皮生长因子活性促进激活,包括连接不稳定和细胞迁移。成熟涉及连接的稳定和功能性内皮屏障的形成。稳定信号的特征和作用机制在很大程度上仍然未知。骨形态发生蛋白受体及其配体在胚胎血管组装和成熟过程中具有重要功能。以前的工作表明生长分化因子 6(GDF6;骨形态发生蛋白 13)在血管完整性中具有作用,尽管 GDF6 的作用机制尚不清楚。因此,我们试图进一步探讨 GDF6 在血管稳定化中的作用。
我们在斑马鱼体内和体外培养的人脐静脉内皮细胞中研究了 GDF6 在促进内皮血管完整性中的作用。我们报告 GDF6 通过拮抗血管内皮生长因子活性促进血管完整性。GDF6 缺陷的内皮细胞具有更高的血管内皮生长因子信号,血管内皮钙黏蛋白 Y658 磷酸化增加,血管内皮钙黏蛋白从细胞-细胞界面定位,并减弱内皮细胞黏附连接,使血管容易渗漏。
我们的结果表明,GDF6 通过抑制血管内皮生长因子信号来促进血管稳定。了解 GDF6 如何影响血管完整性可能有助于深入了解人类出血和相关血管病变。