How VE-cadherin goes with the flow

Vascular endothelial cells respond to changes in blood fl ow (1). Increased fl ow, for example, causes vasodilation and blood vessel remodeling. Collectively, these responses are critical for both vascular development and the maintenance of adult blood vessels. Moreover, disturbed blood fl ow patterns—at artery branch points, for instance—can activate infl ammatory pathways that may initiate the formation of atherosclerotic plaques. Coon et al. reveal that the transmembrane domain of the cell adhesion molecule VE-cadherin mediates fl ow signaling by binding to the growth factor receptors VEGFR2 and VEGFR3 (2). A decade ago, Martin Schwartz and colleagues discovered that VE-cadherin, VEGFR2, and the adhesion molecule PECAM-1 form a mechanosensory complex at endothelial cell–cell junctions (3). PECAM-1 appears to transduce the mechanical forces generated by blood fl ow (4), leading to the ligand-independent activation of VEGFR2 and the initiation of downstream signaling pathways. “But the function of VE-cadherin was a bit mysterious,” explains Schwartz, who now works at Yale University in New Haven, Connecticut. “We wanted to understand its role in fl uid shear stress signaling.” Whatever VE-cadherin does, it’s a function that isn’t shared by other members of the cadherin family. Endo thelial cells lacking VE-cadherin maintain their intercellular adhesions by up-regulating its close homologue N-cadherin, but these cells are unable to respond to fluid shear stress. Schwartz and colleagues, led by postdoc Brian Coon, therefore generated a series of chimeric proteins containing different parts of VEand N-cadherin and determined which of them were able to restore fl ow signaling to VE-cadherin–defi cient mouse cells (2). “To our absolute astonishment, the crucial region was VE-cadherin’s transmembrane domain,” Schwartz says. Chimeric proteins containing this region enabled endothelial cells to respond to fl uid shear stress, whereas chimeras containing VE-cadherin’s extracellular and cytoplasmic domains, but N-cadherin’s transmembrane domain, were unable to support fl ow signaling. Coon et al. therefore looked for proteins that specifi cally bound to VE-cadherin’s transmembrane domain and identified VEGFR3. “That was also a surprise,” Schwartz explains, “because we’d previously found that VEGFR2 was the key component of this junctional mechanosensory complex.” In fact, the researchers discovered, the transmembrane domains of VEGFR2 and VEGFR3 bind equally well to the transmembrane domain of VE-cadherin, and both receptors are activated in response to fl uid shear stress. “It seems that they can substitute for each other, at least for the outputs that we looked at,” says Schwartz, referring, for example, to the activation of proinfl ammatory signaling pathways in endothelial cells subjected to oscillatory shear stress in vitro. To investigate whether VEGFR3 contributed to endothelial fl ow signaling in vivo, Coon et al. fi rst examined the receptor’s expression pattern in mice. VEGFR3 expression is relatively low in adult arteries, but the researchers found that it was somewhat up-regulated at the aortic arch, a site of disturbed blood flow where chronic infl ammation can lead to atherosclerosis. Knocking out Vegfr3 reduced the activation of proinfl ammatory pathways at this site. Thus, VEGFR3, along with VEGFR2, activates fl ow signaling pathways downstream of PECAM-1 and VE-cadherin. In another recent paper, Schwartz and colleagues found that different parts of the vascular system are set to respond to different levels of fl uid shear stress and that the levels of VEGFR3 expression determine what this set point is (5). The researchers think that VE-cadherin acts as an adapter molecule that links the mechanosensory complex’s components together, allowing the mechanical forces transduced by PECAM-1 to transactivate the VEGFRs, perhaps via the Src family kinase Fyn. Having established that VE-cadherin’s transmembrane domain binds to VEGFR2 and VEGFR3, Schwartz now wants to examine the adhesion molecule’s interaction with PECAM-1.