Vascular endothelial-cadherin tyrosine phosphorylation in angiogenic and quiescent adult tissues

التفاصيل البيبلوغرافية
العنوان: Vascular endothelial-cadherin tyrosine phosphorylation in angiogenic and quiescent adult tissues
المؤلفون: Lambeng, Nathalie, Wallez, Yann, Rampon, Christine, Cand, Francine, Christé, Georges, Gulino-Debrac, Danielle, Vilgrain, Isabelle, Huber, Philippe
المساهمون: Laboratoire de développement et vieillissement de l'endothélium, Institut National de la Santé et de la Recherche Médicale (INSERM)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Joseph Fourier - Grenoble 1 (UJF), Institut de biologie structurale (IBS - UMR 5075 ), Université Grenoble Alpes [2016-2019] (UGA [2016-2019])-Institut de Recherche Interdisciplinaire de Grenoble (IRIG), Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Centre National de la Recherche Scientifique (CNRS)
المصدر: Circulation Research
Circulation Research, American Heart Association, 2005, 96 (3), pp.384-91. ⟨10.1161/01.RES.0000156652.99586.9f⟩
بيانات النشر: HAL CCSD, 2005.
سنة النشر: 2005
مصطلحات موضوعية: MESH: Ovary, endothelium, MESH: Umbilical Veins, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, MESH: Cadherins, angiogenesis, VE-cadherin, MESH: Mice, Inbred C57BL, MESH: Gonadotropins, Equine, MESH: Cell Extracts, MESH: Animals, MESH: Proteins, MESH: Endothelial Cells, MESH: Mice, MESH: Humans, MESH: Phosphorylation, MESH: Vascular Endothelial Growth Factor Receptor-2, tyrosine kinase, MESH: Proto-Oncogene Proteins pp60(c-src), MESH: Cell Line, MESH: Vanadates, MESH: Uterus, MESH: Endothelium, Vascular, MESH: Female, MESH: Neovascularization, Physiologic, MESH: Phosphotyrosine
الوصف: International audience; Vascular endothelial-cadherin (VE-cadherin) plays a key role in angiogenesis and in vascular permeability. The regulation of its biological activity may be a central mechanism in normal or pathological angiogenesis. VE-cadherin has been shown to be phosphorylated on tyrosine in vitro under various conditions, including stimulation by VEGF. In the present study, we addressed the question of the existence of a tyrosine phosphorylated form of VE-cadherin in vivo, in correlation with the quiescent versus angiogenic state of adult tissues. Phosphorylated VE-cadherin was detected in mouse lung, uterus, and ovary but not in other tissues unless mice were injected with peroxovanadate to block protein phosphatases. Remarkably, VE-cadherin tyrosine phosphorylation was dramatically increased in uterus and ovary, and not in other organs, during PMSG/hCG-induced angiogenesis. In parallel, we observed an increased association of VE-cadherin with Flk1 (VEGF receptor 2) during hormonal angiogenesis. Additionally, Src kinase was constitutively associated with VE-cadherin in both quiescent and angiogenic tissues and increased phosphorylation of VE-cadherin-associated Src was detected in uterus and ovary after hormonal treatment. Src-VE-cadherin association was detected in cultured endothelial cells, independent of VE-cadherin phosphorylation state and Src activation level. In this model, Src inhibition impaired VEGF-induced VE-cadherin phosphorylation, indicating that VE-cadherin phosphorylation was dependent on Src activation. We conclude that VE-cadherin is a substrate for tyrosine kinases in vivo and that its phosphorylation, together with that of associated Src, is increased by angiogenic stimulation. Physical association between Flk1, Src, and VE-cadherin may thus provide an efficient mechanism for amplification and perpetuation of VEGF-stimulated angiogenic processes.
اللغة: English
تدمد: 0009-7330
1524-4571
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2592::566b3c96ebbbbc7f9fee2c4f0d617b31
https://www.hal.inserm.fr/inserm-00433466/file/Lambeng_Fig_4.pdf
رقم الأكسشن: edsair.od......2592..566b3c96ebbbbc7f9fee2c4f0d617b31
قاعدة البيانات: OpenAIRE