S1PR1 regulates the quiescence of lymphatic vessels by inhibiting laminar shear stress-dependent VEGF-C signaling

JCI Insight. 2020 Jul 23;5(14):e137652. doi: 10.1172/jci.insight.137652.


During the growth of lymphatic vessels (lymphangiogenesis), lymphatic endothelial cells (LECs) at the growing front sprout by forming filopodia. Those tip cells are not exposed to circulating lymph, as they are not lumenized. In contrast, LECs that trail the growing front are exposed to shear stress, become quiescent, and remodel into stable vessels. The mechanisms that coordinate the opposed activities of lymphatic sprouting and maturation remain poorly understood. Here, we show that the canonical tip cell marker Delta-like 4 (DLL4) promotes sprouting lymphangiogenesis by enhancing VEGF-C/VEGF receptor 3 (VEGFR3) signaling. However, in lumenized lymphatic vessels, laminar shear stress (LSS) inhibits the expression of DLL4, as well as additional tip cell markers. Paradoxically, LSS also upregulates VEGF-C/VEGFR3 signaling in LECs, but sphingosine 1-phosphate receptor 1 (S1PR1) activity antagonizes LSS-mediated VEGF-C signaling to promote lymphatic vascular quiescence. Correspondingly, S1pr1 loss in LECs induced lymphatic vascular hypersprouting and hyperbranching, which could be rescued by reducing Vegfr3 gene dosage in vivo. In addition, S1PR1 regulates lymphatic vessel maturation by inhibiting RhoA activity to promote membrane localization of the tight junction molecule claudin-5. Our findings suggest a potentially new paradigm in which LSS induces quiescence and promotes the survival of LECs by downregulating DLL4 and enhancing VEGF-C signaling, respectively. S1PR1 dampens LSS/VEGF-C signaling, thereby preventing sprouting from quiescent lymphatic vessels. These results also highlight the distinct roles that S1PR1 and DLL4 play in LECs when compared with their known roles in the blood vasculature.

Keywords: Development; G-protein coupled receptors; Signal transduction; Vascular Biology; endothelial cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Proliferation
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Lymphangiogenesis / genetics*
  • Lymphatic Vessels / metabolism
  • Lymphatic Vessels / pathology
  • Membrane Proteins / genetics
  • Mice
  • Pseudopodia / genetics
  • Pseudopodia / metabolism
  • Signal Transduction
  • Sphingosine-1-Phosphate Receptors / genetics*
  • Stress, Mechanical
  • Vascular Endothelial Growth Factor C / genetics*
  • Vascular Endothelial Growth Factor Receptor-3 / genetics*


  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • S1PR1 protein, human
  • Sphingosine-1-Phosphate Receptors
  • VEGFC protein, human
  • Vascular Endothelial Growth Factor C
  • delta protein
  • FLT4 protein, human
  • Vascular Endothelial Growth Factor Receptor-3