Endothelial Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 Is Critical for Lymphatic Vascular Development and Function

Abstract

The molecular mechanisms underlying lymphatic vascular development and function are not well understood. Recent studies have suggested a role for endothelial cell (EC) mitogen-activated protein kinase kinase kinase kinase 4 (Map4k4) in developmental angiogenesis and atherosclerosis. Here, we show that constitutive loss of EC Map4k4 in mice causes postnatal lethality due to chylothorax, suggesting that Map4k4 is required for normal lymphatic vascular function. Mice constitutively lacking EC Map4k4 displayed dilated lymphatic capillaries, insufficient lymphatic valves, and impaired lymphatic flow; furthermore, primary ECs derived from these animals displayed enhanced proliferation compared with controls. Yeast 2-hybrid analyses identified the Ras GTPase-activating protein Rasa1, a known regulator of lymphatic development and lymphatic endothelial cell fate, as a direct interacting partner for Map4k4. Map4k4 silencing in ECs enhanced basal Ras and extracellular signal-regulated kinase (Erk) activities, and primary ECs lacking Map4k4 displayed enhanced lymphatic EC marker expression. Taken together, these results reveal that EC Map4k4 is critical for lymphatic vascular development by regulating EC quiescence and lymphatic EC fate.

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ACKNOWLEDGMENTS

We thank Joseph Virbasius, Silvia Corvera, John Keaney, and Nathan Lawson for helpful discussions, Ozlem Senol-Cosar for technical support, and Joseph Virbasius and Marina DiStefano for critical reading of the manuscript. We also thank the UMASS Morphology core for assistance.

This work was supported by NIH grant DK030898 to M.P.C.

We declare no financial conflicts of interest.

R.J.R.F. and M.P.C. designed the research; R.J.R.F., C.-A.G., J.C.Y., and L.V.D. performed the research; S.G. analyzed gene expression data; Y.J.K.E. provided bioinformatics and IT assistance; and R.J.R.F. and M.P.C. wrote the manuscript.