| First Author | Iyer D | Year | 2023 |
| Journal | Arterioscler Thromb Vasc Biol | Volume | 43 |
| Issue | 11 | Pages | 2197-2212 |
| PubMed ID | 37767708 | Mgi Jnum | J:341378 |
| Mgi Id | MGI:7539040 | Doi | 10.1161/ATVBAHA.123.319405 |
| Citation | Iyer D, et al. (2023) eNOS Regulates Lymphatic Valve Specification by Controlling beta-Catenin Signaling During Embryogenesis in Mice. Arterioscler Thromb Vasc Biol |
| abstractText | BACKGROUND: Lymphatic valves play a critical role in ensuring unidirectional lymph transport. Loss of lymphatic valves or dysfunctional valves are associated with several diseases including lymphedema, lymphatic malformations, obesity, and ileitis. Lymphatic valves first develop during embryogenesis in response to mechanotransduction signaling pathways triggered by oscillatory lymph flow. In blood vessels, eNOS (endothelial NO synthase; gene name: Nos3) is a well-characterized shear stress signaling effector, but its role in lymphatic valve development remains unexplored. METHODS: We used global Nos3(-/-) mice and cultured human dermal lymphatic endothelial cells to investigate the role of eNOS in lymphatic valve development, which requires oscillatory shear stress signaling. RESULTS: Our data reveal a 45% reduction in lymphatic valve specification cell clusters and that loss of eNOS protein inhibited activation of beta-catenin and its nuclear translocation. Genetic knockout or knockdown of eNOS led to downregulation of beta-catenin target proteins in vivo and in vitro. However, pharmacological inhibition of NO production did not reproduce these effects. Co-immunoprecipitation and proximity ligation assays reveal that eNOS directly binds to beta-catenin and their binding is enhanced by oscillatory shear stress. Finally, genetic ablation of the Foxo1 gene enhanced FOXC2 expression and partially rescued the loss of valve specification in the eNOS knockouts. CONCLUSIONS: In conclusion, we demonstrate a novel, NO-independent role for eNOS in regulating lymphatic valve specification and propose a mechanism by which eNOS directly binds beta-catenin to regulate its nuclear translocation and thereby transcriptional activity. |
