Lu Xiaowei, Le Noble Ferdinand, Yuan Li, Jiang Quingjan, De Lafarge Benjamin, Sugiyama Daisuke, Bréant Christiane, Claes Filip, De Smet Frederik, Thomas Jean-Léon, Autiero Monica, Carmeliet Peter, Tessier-Lavigne Marc, Eichmann Anne
Department of Biological Sciences, Howard Hughes Medical Institute, Stanford University, Stanford, California 94305, USA.
Nature. 2004 Nov 11;432(7014):179-86. doi: 10.1038/nature03080. Epub 2004 Oct 27.
Blood vessels and nerves are complex, branched structures that share a high degree of anatomical similarity. Guidance of vessels and nerves has to be exquisitely regulated to ensure proper wiring of both systems. Several regulators of axon guidance have been identified and some of these are also expressed in endothelial cells; however, the extent to which their guidance functions are conserved in the vascular system is still incompletely understood. We show here that the repulsive netrin receptor UNC5B is expressed by endothelial tip cells of the vascular system. Disruption of the Unc5b gene in mice, or of Unc5b or netrin-1a in zebrafish, leads to aberrant extension of endothelial tip cell filopodia, excessive vessel branching and abnormal navigation. Netrin-1 causes endothelial filopodial retraction, but only when UNC5B is present. Thus, UNC5B functions as a repulsive netrin receptor in endothelial cells controlling morphogenesis of the vascular system.
血管和神经是复杂的分支结构,具有高度的解剖学相似性。血管和神经的导向必须精确调节,以确保两个系统的正确布线。已经鉴定出几种轴突导向调节因子,其中一些也在内皮细胞中表达;然而,它们的导向功能在血管系统中的保守程度仍未完全了解。我们在此表明,排斥性的netrin受体UNC5B在血管系统的内皮尖端细胞中表达。小鼠中Unc5b基因的破坏,或斑马鱼中Unc5b或netrin-1a的破坏,会导致内皮尖端细胞丝状伪足的异常延伸、血管分支过多和导航异常。Netrin-1会导致内皮丝状伪足回缩,但仅在存在UNC5B时才会发生。因此,UNC5B在内皮细胞中作为一种排斥性netrin受体发挥作用,控制血管系统的形态发生。