D'Amico Gabriela, Jones Dylan T, Nye Emma, Sapienza Karen, Ramjuan Antoine R, Reynolds Louise E, Robinson Stephen D, Kostourou Vassiliki, Martinez Dolores, Aubyn Deborah, Grose Richard, Thomas Gareth J, Spencer-Dene Bradley, Zicha Daniel, Davies Derek, Tybulewicz Victor, Hodivala-Dilke Kairbaan M
Adhesion and Angiogenesis Laboratory, Institute of Cancer and Cancer Research UK, Bart's & The London Queen Mary's School of Medicine & Dentistry, John Vane Science Centre, Charterhouse Square, London, EC1M 6BQ, UK.
Development. 2009 Dec;136(23):4043-53. doi: 10.1242/dev.035014.
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.
发芽血管生成和淋巴管-血管分离均涉及内皮细胞的迁移,但决定血管内皮细胞分离形成淋巴管系统的精确迁移分子尚不清楚。在此,我们在小鼠中敲除内皮细胞中的Rac1(Tie1-Cre(+);Rac1(fl/fl)),意外地发现,虽然血管形态看起来正常,但淋巴管-血管分离受损,并伴有相应的水肿、出血和胚胎致死性。重要的是,正常水平的Rac1对于内皮细胞对淋巴管诱导信号的定向迁移反应至关重要。我们的研究确定Rac1是内皮细胞分离并形成淋巴管系统所需迁移机制的关键组成部分。