Mfsd2b and Spns2 are essential for maintenance of blood vessels during development and in anaphylactic shock

Sphingosine-1-phosphate (S1P) is a potent lipid mediator that is secreted by several cell types. We recently showed that Mfsd2b is an S1P transporter from hematopoietic cells that contributes approximately 50% plasma S1P. Here we report the characterization of compound deletion of Mfsd2b and Spns2, another S1P transporter active primarily in endothelial cells. Global deletion of Mfsd2b and Spns2 (global double knockout [gDKO]) results in embryonic lethality beyond embryonic day 14.5 (E14.5), with severe hemorrhage accompa-nied by defects of tight junction proteins, indicating that Mfsd2b and Spns2 provide S1P for signaling, which is essential for blood vessel integrity. Compound postnatal deletion of Mfsd2b and Spns2 using Mx1Cre (ctDKO-Mx1Cre) results in maximal 80% reduction of plasma S1P. ctDKO-Mx1Cre mice exhibit severe susceptibility to anaphylaxis, indicating that S1P from Mfsd2b and Spns2 is indispensable for vascular homeostasis. Our re-sults show that S1P export from Mfsd2b and Spns2 is essential for developing and mature vasculature.

Automated summary

This study highlights the importance of S1P transporters Mfsd2b and Spns2 in maintaining vascular integrity and homeostasis. Global deletion of these transporters leads to embryonic lethality, while postnatal deletion increases susceptibility to anaphylaxis in mice.