Neurodegeneration Labs, Department of Neuroscience, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
Dev Cell. 2012 Feb 14;22(2):403-17. doi: 10.1016/j.devcel.2011.11.018.
Signaling events that regulate central nervous system (CNS) angiogenesis and blood-brain barrier (BBB) formation are only beginning to be elucidated. By evaluating the gene expression profile of mouse vasculature, we identified DR6/TNFRSF21 and TROY/TNFRSF19 as regulators of CNS-specific angiogenesis in both zebrafish and mice. Furthermore, these two death receptors interact both genetically and physically and are required for vascular endothelial growth factor (VEGF)-mediated JNK activation and subsequent human brain endothelial sprouting in vitro. Increasing beta-catenin levels in brain endothelium upregulate DR6 and TROY, indicating that these death receptors are downstream target genes of Wnt/beta-catenin signaling, which has been shown to be required for BBB development. These findings define a role for death receptors DR6 and TROY in CNS-specific vascular development.
调控中枢神经系统(CNS)血管生成和血脑屏障(BBB)形成的信号事件才刚刚开始被阐明。通过评估小鼠血管的基因表达谱,我们发现 DR6/TNFRSF21 和 TROY/TNFRSF19 是在斑马鱼和小鼠中调节 CNS 特异性血管生成的调节剂。此外,这两种死亡受体在遗传和物理上相互作用,并且是血管内皮生长因子(VEGF)介导的 JNK 激活以及随后体外人脑内皮芽生所必需的。在脑内皮细胞中增加β-连环蛋白水平会上调 DR6 和 TROY,表明这些死亡受体是 Wnt/β-连环蛋白信号的下游靶基因,已显示其对于 BBB 的发育是必需的。这些发现定义了死亡受体 DR6 和 TROY 在 CNS 特异性血管发育中的作用。