Regulation of lymphatic-blood vessel separation by endothelial Rac1
Author(s) -
Gabriela D’Amico,
Dylan T. Jones,
Emma Nye,
Karen Sapienza,
Antoine R. Ramjuan,
Louise E. Reynolds,
Stephen D. Robinson,
Vassiliki Kostourou,
Dolores Martínez,
Deborah Aubyn,
Richard Grose,
Gareth J. Thomas,
Bradley SpencerDene,
Daniel Zicha,
Derek Davies,
Victor L. J. Tybulewicz,
Kairbaan HodivalaDilke
Publication year - 2009
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.035014
Subject(s) - lymphatic system , biology , sprouting angiogenesis , lymphatic endothelium , blood vessel , lymphangiogenesis , rac1 , angiogenesis , lymphatic vessel , endothelial stem cell , endothelium , microbiology and biotechnology , vascular endothelial growth factor c , pathology , neovascularization , anatomy , immunology , cancer research , vascular endothelial growth factor a , signal transduction , endocrinology , vascular endothelial growth factor , cancer , genetics , medicine , metastasis , vegf receptors , in vitro
Sprouting angiogenesis and lymphatic-blood vessel segregation both involve the migration of endothelial cells, but the precise migratory molecules that govern the decision of blood vascular endothelial cells to segregate into lymphatic vasculature are unknown. Here, we deleted endothelial Rac1 in mice (Tie1-Cre(+);Rac1(fl/fl)) and revealed, unexpectedly, that whereas blood vessel morphology appeared normal, lymphatic-blood vessel separation was impaired, with corresponding edema, haemorrhage and embryonic lethality. Importantly, normal levels of Rac1 were essential for directed endothelial cell migratory responses to lymphatic-inductive signals. Our studies identify Rac1 as a crucial part of the migratory machinery required for endothelial cells to separate and form lymphatic vasculature.
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