Carbon monoxide inhibits sprouting angiogenesis and vascular endothelial growth factor receptor-2 phosphorylation

Carbon monoxide (CO) is a gaseous autacoid known to positively regulate vascular tone; however, its role in angiogenesis is unknown. The aim of this study was to investigate the effect of CO on angiogenesis and vascular endothelial growth factor (VEGF) receptor-2 phosphorylation. Human umbilical vei...

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Publicado: 2015
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03406245_v113_n2_p329_Ahmad
http://hdl.handle.net/20.500.12110/paper_03406245_v113_n2_p329_Ahmad
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spelling paper:paper_03406245_v113_n2_p329_Ahmad2023-06-08T15:34:07Z Carbon monoxide inhibits sprouting angiogenesis and vascular endothelial growth factor receptor-2 phosphorylation Angiogenesis Carbon monoxide Endothelial cells Vascular endothelial growth factor Vascular endothelial growth factor receptor-2 actin carbon monoxide cytochrome c oxidase fibroblast growth factor 2 protein kinase B protein tyrosine phosphatase tyrosine vasculotropin receptor 2 carbon monoxide collagen drug combination laminin matrigel organometallic compound proteoglycan recombinant protein tricarbonyldichlororuthenium (II) dimer tyrosine vascular endothelial growth factor receptor-2, human vasculotropin receptor 2 angiogenesis angiogenesis assay animal experiment animal tissue Article cancer inhibition cell migration assay cell proliferation assay controlled study down regulation drug mechanism human human cell immunoprecipitation mouse nonhuman priority journal protein phosphorylation umbilical vein endothelial cell Western blotting animal C57BL mouse cell motion cell proliferation chemistry cytology drug combination endothelium cell metabolism neovascularization (pathology) phosphorylation Animals Carbon Monoxide Cell Movement Cell Proliferation Collagen Drug Combinations Endothelial Cells Human Umbilical Vein Endothelial Cells Humans Immunoprecipitation Laminin Mice, Inbred C57BL Neovascularization, Pathologic Organometallic Compounds Phosphorylation Proteoglycans Recombinant Proteins Tyrosine Vascular Endothelial Growth Factor Receptor-2 Carbon monoxide (CO) is a gaseous autacoid known to positively regulate vascular tone; however, its role in angiogenesis is unknown. The aim of this study was to investigate the effect of CO on angiogenesis and vascular endothelial growth factor (VEGF) receptor-2 phosphorylation. Human umbilical vein endothelial cells (HUVECs) were cultured on growth factor- reduced Matrigel and treated with a CO-releasing molecule (CORM-2) or exposed to CO gas (250 ppm). Here, we report the surprising finding that exposure to CO inhibits vascular endothelial growth factor (VEGF)-induced endothelial cell actin reorganisation, cell proliferation, migration and capillary-like tube formation. Similarly, CO suppressed VEGF-mediated phosphorylation of VEGFR-2 at tyrosine residue 1175 and 1214 and basic fibroblast growth factor- (FGF-2) and VEGF-mediated Akt phosphorylation. Consistent with these data, mice exposed to 250 ppm CO (1h/day for 14 days) exhibited a marked decrease in FGF-2-induced Matrigel plug angiogenesis (p<0.05). These data establish a new biological function for CO in angiogenesis and point to a potential therapeutic use for CO as an anti-angiogenic agent in tumour suppression. © Schattauer 2015. 2015 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03406245_v113_n2_p329_Ahmad http://hdl.handle.net/20.500.12110/paper_03406245_v113_n2_p329_Ahmad
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Angiogenesis
Carbon monoxide
Endothelial cells
Vascular endothelial growth factor
Vascular endothelial growth factor receptor-2
actin
carbon monoxide
cytochrome c oxidase
fibroblast growth factor 2
protein kinase B
protein tyrosine phosphatase
tyrosine
vasculotropin receptor 2
carbon monoxide
collagen
drug combination
laminin
matrigel
organometallic compound
proteoglycan
recombinant protein
tricarbonyldichlororuthenium (II) dimer
tyrosine
vascular endothelial growth factor receptor-2, human
vasculotropin receptor 2
angiogenesis
angiogenesis assay
animal experiment
animal tissue
Article
cancer inhibition
cell migration assay
cell proliferation assay
controlled study
down regulation
drug mechanism
human
human cell
immunoprecipitation
mouse
nonhuman
priority journal
protein phosphorylation
umbilical vein endothelial cell
Western blotting
animal
C57BL mouse
cell motion
cell proliferation
chemistry
cytology
drug combination
endothelium cell
metabolism
neovascularization (pathology)
phosphorylation
Animals
Carbon Monoxide
Cell Movement
Cell Proliferation
Collagen
Drug Combinations
Endothelial Cells
Human Umbilical Vein Endothelial Cells
Humans
Immunoprecipitation
Laminin
Mice, Inbred C57BL
Neovascularization, Pathologic
Organometallic Compounds
Phosphorylation
Proteoglycans
Recombinant Proteins
Tyrosine
Vascular Endothelial Growth Factor Receptor-2
spellingShingle Angiogenesis
Carbon monoxide
Endothelial cells
Vascular endothelial growth factor
Vascular endothelial growth factor receptor-2
actin
carbon monoxide
cytochrome c oxidase
fibroblast growth factor 2
protein kinase B
protein tyrosine phosphatase
tyrosine
vasculotropin receptor 2
carbon monoxide
collagen
drug combination
laminin
matrigel
organometallic compound
proteoglycan
recombinant protein
tricarbonyldichlororuthenium (II) dimer
tyrosine
vascular endothelial growth factor receptor-2, human
vasculotropin receptor 2
angiogenesis
angiogenesis assay
animal experiment
animal tissue
Article
cancer inhibition
cell migration assay
cell proliferation assay
controlled study
down regulation
drug mechanism
human
human cell
immunoprecipitation
mouse
nonhuman
priority journal
protein phosphorylation
umbilical vein endothelial cell
Western blotting
animal
C57BL mouse
cell motion
cell proliferation
chemistry
cytology
drug combination
endothelium cell
metabolism
neovascularization (pathology)
phosphorylation
Animals
Carbon Monoxide
Cell Movement
Cell Proliferation
Collagen
Drug Combinations
Endothelial Cells
Human Umbilical Vein Endothelial Cells
Humans
Immunoprecipitation
Laminin
Mice, Inbred C57BL
Neovascularization, Pathologic
Organometallic Compounds
Phosphorylation
Proteoglycans
Recombinant Proteins
Tyrosine
Vascular Endothelial Growth Factor Receptor-2
Carbon monoxide inhibits sprouting angiogenesis and vascular endothelial growth factor receptor-2 phosphorylation
topic_facet Angiogenesis
Carbon monoxide
Endothelial cells
Vascular endothelial growth factor
Vascular endothelial growth factor receptor-2
actin
carbon monoxide
cytochrome c oxidase
fibroblast growth factor 2
protein kinase B
protein tyrosine phosphatase
tyrosine
vasculotropin receptor 2
carbon monoxide
collagen
drug combination
laminin
matrigel
organometallic compound
proteoglycan
recombinant protein
tricarbonyldichlororuthenium (II) dimer
tyrosine
vascular endothelial growth factor receptor-2, human
vasculotropin receptor 2
angiogenesis
angiogenesis assay
animal experiment
animal tissue
Article
cancer inhibition
cell migration assay
cell proliferation assay
controlled study
down regulation
drug mechanism
human
human cell
immunoprecipitation
mouse
nonhuman
priority journal
protein phosphorylation
umbilical vein endothelial cell
Western blotting
animal
C57BL mouse
cell motion
cell proliferation
chemistry
cytology
drug combination
endothelium cell
metabolism
neovascularization (pathology)
phosphorylation
Animals
Carbon Monoxide
Cell Movement
Cell Proliferation
Collagen
Drug Combinations
Endothelial Cells
Human Umbilical Vein Endothelial Cells
Humans
Immunoprecipitation
Laminin
Mice, Inbred C57BL
Neovascularization, Pathologic
Organometallic Compounds
Phosphorylation
Proteoglycans
Recombinant Proteins
Tyrosine
Vascular Endothelial Growth Factor Receptor-2
description Carbon monoxide (CO) is a gaseous autacoid known to positively regulate vascular tone; however, its role in angiogenesis is unknown. The aim of this study was to investigate the effect of CO on angiogenesis and vascular endothelial growth factor (VEGF) receptor-2 phosphorylation. Human umbilical vein endothelial cells (HUVECs) were cultured on growth factor- reduced Matrigel and treated with a CO-releasing molecule (CORM-2) or exposed to CO gas (250 ppm). Here, we report the surprising finding that exposure to CO inhibits vascular endothelial growth factor (VEGF)-induced endothelial cell actin reorganisation, cell proliferation, migration and capillary-like tube formation. Similarly, CO suppressed VEGF-mediated phosphorylation of VEGFR-2 at tyrosine residue 1175 and 1214 and basic fibroblast growth factor- (FGF-2) and VEGF-mediated Akt phosphorylation. Consistent with these data, mice exposed to 250 ppm CO (1h/day for 14 days) exhibited a marked decrease in FGF-2-induced Matrigel plug angiogenesis (p<0.05). These data establish a new biological function for CO in angiogenesis and point to a potential therapeutic use for CO as an anti-angiogenic agent in tumour suppression. © Schattauer 2015.
title Carbon monoxide inhibits sprouting angiogenesis and vascular endothelial growth factor receptor-2 phosphorylation
title_short Carbon monoxide inhibits sprouting angiogenesis and vascular endothelial growth factor receptor-2 phosphorylation
title_full Carbon monoxide inhibits sprouting angiogenesis and vascular endothelial growth factor receptor-2 phosphorylation
title_fullStr Carbon monoxide inhibits sprouting angiogenesis and vascular endothelial growth factor receptor-2 phosphorylation
title_full_unstemmed Carbon monoxide inhibits sprouting angiogenesis and vascular endothelial growth factor receptor-2 phosphorylation
title_sort carbon monoxide inhibits sprouting angiogenesis and vascular endothelial growth factor receptor-2 phosphorylation
publishDate 2015
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03406245_v113_n2_p329_Ahmad
http://hdl.handle.net/20.500.12110/paper_03406245_v113_n2_p329_Ahmad
_version_ 1768544366537736192