Dopamine in vivo inhibits VEGF-induced phosphorylation of VEGFR-2, MAPK, and focal adhesion kinase in endothelial cells
Autor: | Rita Mitra, Samir Banerjee, Sujit Basu, Partha Sarathi Dasgupta, Chandrani Sarkar, Debanjan Chakroborty |
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Rok vydání: | 2004 |
Předmět: |
MAPK/ERK pathway
Male Vascular Endothelial Growth Factor A medicine.medical_specialty Physiology MAP Kinase Signaling System medicine.medical_treatment Dopamine Neovascularization Physiologic Biology Focal adhesion Mice Vasculogenesis Physiology (medical) Internal medicine medicine Animals Phosphorylation Mice Knockout Receptors Dopamine D2 Growth factor Ascites Kinase insert domain receptor Protein-Tyrosine Kinases Vascular Endothelial Growth Factor Receptor-2 Cell biology Mesenteric Arteries Endothelial stem cell Mice Inbred C57BL Endocrinology Cytokine Focal Adhesion Kinase 1 Focal Adhesion Protein-Tyrosine Kinases Endothelium Vascular Signal transduction Mitogen-Activated Protein Kinases Peritoneum Cardiology and Cardiovascular Medicine |
Zdroj: | American journal of physiology. Heart and circulatory physiology. 287(4) |
ISSN: | 0363-6135 |
Popis: | Vascular permeability factor (VPF)/VEGF is a potent multifunctional cytokine and growth factor that has critical roles in vasculogenesis and in both physiological and pathological angiogenesis. Because it has been recently shown that the neurotransmitter dopamine at pharmacological dose can inhibit VEGF/VPF-mediated microvascular permeability, proliferation, and migration of endothelial cells in vitro, we therefore hypothesized that endogenous dopamine may regulate the actions of VPF/VEGF in vivo. We report that VPF/VEGF-induced phosphorylation of VEGF receptor 2, focal adhesion kinase, and MAPK in the endothelial cells is strikingly increased in both dopamine-depleted and dopamine D2 receptor knockout mice compared with normal controls, thereby indicating that endogenous dopamine regulate these critical signaling cascades required for the in vivo endothelial functions of VPF/VEGF. Together, these observations provide new mechanistic insight into the dopamine-mediated inhibition of the activities of VPF/VEGF and suggest that endogenous neurotransmitter dopamine might be an important physiological regulator of VPF/VEGF activities in vivo. |
Databáze: | OpenAIRE |
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