Abstract

SummaryAngiogenesis, the process by which new blood vessels arise from preexisting ones, is critical for embryonic development and is an integral part of many disease processes. Recent studies have provided detailed information on how angiogenic sprouts initiate, elongate, and branch, but less is known about how these processes cease. Here, we show that S1PR1, a receptor for the blood-borne bioactive lipid sphingosine-1-phosphate (S1P), is critical for inhibition of angiogenesis and acquisition of vascular stability. Loss of S1PR1 leads to increased endothelial cell sprouting and the formation of ectopic vessel branches. Conversely, S1PR1 signaling inhibits angiogenic sprouting and enhances cell-to-cell adhesion. This correlates with inhibition of vascular endothelial growth factor-A (VEGF-A)-induced signaling and stabilization of vascular endothelial (VE)-cadherin localization at endothelial junctions. Our data suggest that S1PR1 signaling acts as a vascular-intrinsic stabilization mechanism, protecting developing blood vessels against aberrant angiogenic responses.Highlights•Sphingosine-1-phosphate receptor-1 (Edg1) is a negative regulator of angiogenesis•Loss of S1pr1 (Edg1) causes endothelial hyperplasia and derangement of the aorta•S1PR1 (Edg1) regulates cellular adhesion, motility, and VE-cadherin localization•S1PR1 (Edg1) regulates VEGF-induced VEGFR2 signaling and internalization