Abstract
Divalent cobalt ions (Co2+) induce the expression of hypoxia responsive genes and are often used in cell biology to mimic hypoxia. In this in vitro study we compared the effects of hypoxia and Co2+ on human endothelial cells and examined processes that are stimulated in hypoxia in vivo (proliferation and angiogenesis). We analyzed the expression of the hypoxia-inducible factor-1alpha (HIF-1alpha) under different hypoxic conditions (3% and nearly 0% O2) and Co2+ -concentrations (0.01-0.7 mM). As in hypoxia, the amount of HIF-1alpha protein was enhanced by exposure to Co2+ (did not correlate with mRNA amount). however, contrary to the results of hypoxia, in vitro-angiogenesis was inhibited after exposure to even low Co2+-concentrations (> or =0.01 mM). This led to the conclusion that although hypoxia signaling after Co2+ -exposure took place, further yet unknown Co2+ -induced event(s) must have occurred.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cell Line
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Cell Proliferation
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Cells, Cultured
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Cobalt / metabolism
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Cobalt / pharmacology*
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Coloring Agents / pharmacology
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Endothelium, Vascular / cytology
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Endothelium, Vascular / pathology*
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Enzyme-Linked Immunosorbent Assay
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Gentian Violet / pharmacology
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Humans
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Hypoxia*
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Hypoxia-Inducible Factor 1, alpha Subunit
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Immunoenzyme Techniques
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In Vitro Techniques
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Ions*
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Ki-67 Antigen / biosynthesis
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Microscopy, Fluorescence
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Neovascularization, Pathologic*
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Oxygen / metabolism
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RNA, Messenger / metabolism
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Reverse Transcriptase Polymerase Chain Reaction
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Signal Transduction
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Software
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Transcription Factors / metabolism
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Vascular Endothelial Growth Factor A / metabolism
Substances
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Coloring Agents
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HIF1A protein, human
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Hypoxia-Inducible Factor 1, alpha Subunit
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Ions
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Ki-67 Antigen
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RNA, Messenger
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Transcription Factors
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Vascular Endothelial Growth Factor A
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Cobalt
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Gentian Violet
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Oxygen