, 2010), while expression of angiopoietin-2 (Ang2), an Ang1 antagonist, was enhanced. Neural progenitors also participate in establishing the BBB by secreting Wnt ligands that activate β-catenin signaling in ECs (Figure 3). Genetic studies show that β-catenin signaling in ECs in vivo is required to induce and maintain BBB properties such as the expression of the glucose transporter Glut1 and the tight junction molecule claudin3 (Daneman et al., 2009, Liebner et al., 2008 and Stenman et al., 2008). Moreover, αvβ8 integrin-mediated adhesion

of neural progenitors and their glial progeny to the neurovascular unit are required for morphogenesis of the forebrain vasculature. Indeed, deletion of αvβ8 in neural progenitors results in the formation of misshaped EC clusters and cerebral hemorrhage despite basement membrane formation and pericyte coverage (McCarty, 2009). More PI3K cancer than five centuries ago, the Belgian anatomist Vesalius discovered that nerves and vessels track along each other to reach their target. The vascular and nervous system display intriguing parallelisms in their stereotyped architectural patterning and functional organization (Carmeliet and Tessier-Lavigne, 2005). Explanations for this copatterning mTOR inhibitor are that neurons and ECs respond to

the same (classes of) molecular cues, or that they coregulate each other’s migration. As the vascular system developed later in evolution than the nervous system, vessels are believed to have co-opted some of the genetic pathways for similar biological processes. Four classical axon guidance cue families Sclareol (netrins, slits, ephrins, semaphorins) guide growth cones of axons and regulate navigation of endothelial tip cells via similar principles of repulsion and attraction, which we will illustrate here only with a few (recent) prototypic examples. Endothelial tip cells extend filopodia that explore their surroundings for guidance cues. Neuropilin-1 (Nrp1) was discovered as a receptor for semaphorins in repulsive axon guidance but is also a coreceptor for VEGF and other

angiogenic factors on ECs (Carmeliet and Tessier-Lavigne, 2005). Nrp1 null embryos succumb due to cardiovascular malformations because of an interrupted interaction with VEGF (Fantin et al., 2009 and Rosenstein et al., 2010). Nrp1 blockade is currently being evaluated as novel anti-angiogenic strategy for the treatment of cancer (Bagri et al., 2009). Semaphorins, other ligands of Nrp1, usually inhibit angiogenesis, though some can also be stimulatory (Capparuccia and Tamagnone, 2009). By activating Plexin-D1 directly, semaphorin 3E (Sema3E) controls vessel navigation via distinct mechanisms. In intersomitic vessels in zebrafish embryos, Sema3E, produced by perivascular cells, prevents ECs from erroneous navigation in unwanted territories, presumably by reorienting the cytoskeleton of the tip cell itself.