Abluminal stimulation of sphingosine 1-phosphate receptors 1 and 3 promotes and stabilizes endothelial sprout formation

• Published in: Tissue engineering. Part A Vol. 21; no. 1-2; p. 202
• Main Authors: Das, Anusuya, Lenz, Steven M, Awojoodu, Anthony O, Botchwey, Edward A
• Format: Journal Article
• Language: English
• Published: United States 01-01-2015
• Subjects: Animals; Antigens, CD; Aorta - cytology; Cadherins; Cell Movement - drug effects; Diffusion; Endothelial Cells - drug effects; Endothelial Cells - metabolism; Human Umbilical Vein Endothelial Cells - drug effects; Human Umbilical Vein Endothelial Cells - metabolism; Humans; In Vitro Techniques; Male; Mice, Inbred C57BL; Neovascularization, Physiologic; Receptors, Lysosphingolipid - agonists; Receptors, Lysosphingolipid - antagonists & inhibitors; Receptors, Lysosphingolipid - metabolism; Vascular Endothelial Growth Factor A - pharmacology
• ISSN: 1937-335X
• DOI: 10.1089/ten.tea.2013.0744

Local delivery of lipid mediators has become a promising new approach for therapeutic angiogenesis and regenerative medicine. In this study, we investigated how gradient stimulation (either abluminal/distal or luminal/proximal) of engineered microvessels with sphingosine 1-phosphate (S1P) receptor-subtype-targeted molecules affects endothelial sprout growth using a microfluidic device. Our studies show that distal stimulation of microvessels with FTY720, an S1P1/3 selective agonist, promotes both arterial and venular sprout growth, whereas proximal stimulation does not. Using novel pharmacological antagonists of S1P receptor subtypes, we further show that S1P3 functionality is necessary for VEGF-induced sprouting, and confirmed these findings ex vivo using a murine aortic ring assay from S1P3-deficient mice. S1P3 agonist stimulation enhanced vascular stability in both cell types via upregulation of the interendothelial junction protein VE-cadherin. Lastly, S1P3 activation under flow promoted endothelial sprouting and branching while decreasing migratory cell fate in the microfluidic device. We used an in vivo murine dorsal skinfold window chamber model to confirm S1P3's role in neovascular branching. Together, these data suggest that a distal transendothelial gradient of S1P1/3-targeted drugs is an effective technique for both enhancing and stabilizing capillary morphogenesis in angiogenic applications.