Identification of Membrane Calcium Channels Essential for Cytoplasmic and Nuclear Calcium Elevations Induced by Vascular Endothelial Growth Factor in Human Endothelial Cells

Autor: Stéphanie Garnier-Raveaud, Michel Robert-Nicoud, Yves Usson, Francine Cand, Gilles Faury, Jean Verdetti
Přispěvatelé: RFMQ, Techniques de l'Ingénierie Médicale et de la Complexité - Informatique, Mathématiques et Applications, Grenoble - UMR 5525 (TIMC-IMAG), Université Joseph Fourier - Grenoble 1 (UJF)-Centre National de la Recherche Scientifique (CNRS)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Université Joseph Fourier - Grenoble 1 (UJF)-Centre National de la Recherche Scientifique (CNRS)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS), Usson, Yves, VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF)
Rok vydání: 2001
Předmět:
Vascular Endothelial Growth Factor A
Cytoplasm
Umbilical Veins
Patch-Clamp Techniques
[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/Imaging
Angiogenesis
Clinical Biochemistry
Endothelial Growth Factors
MESH: Vascular Endothelial Growth Factors
Calcium in biology
MESH: Endothelial Growth Factors
0302 clinical medicine
Endocrinology
Nickel
MESH: Nickel
MESH: Microscopy
Confocal

Cells
Cultured

Lymphokines
0303 health sciences
MESH: Electrophysiology
Microscopy
Confocal

Voltage-dependent calcium channel
Vascular Endothelial Growth Factors
MESH: Infant
Newborn

Cell biology
Electrophysiology
Vascular endothelial growth factor B
Vascular endothelial growth factor A
MESH: Calcium
030220 oncology & carcinogenesis
MESH: Calcium Channels
MESH: Cell Division
MESH: Endothelium
Vascular

Cell Division
MESH: Cells
Cultured

MESH: Cell Nucleus
Transcriptional Activation
Inositol Phosphates
Recombinant Fusion Proteins
MESH: Umbilical Veins
chemistry.chemical_element
Calcium
Biology
03 medical and health sciences
MESH: Patch-Clamp Techniques
MESH: Recombinant Fusion Proteins
Humans
030304 developmental biology
Cell Nucleus
MESH: Humans
MESH: Lymphokines
MESH: Vascular Endothelial Growth Factor A
MESH: Cytoplasm
Calcium channel
Cell Membrane
Infant
Newborn

T-type calcium channel
Cell Biology
MESH: Inositol Phosphates
[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/Imaging
chemistry
MESH: Trans-Activation (Genetics)
Calcium Channels
Endothelium
Vascular

MESH: Cell Membrane
Zdroj: Growth Factors
Growth Factors, Taylor & Francis, 2001, 19 (1), pp.35-48
ISSN: 1029-2292
0897-7194
Popis: Vascular endothelial growth factor (VEGF) is mitogenic for endothelial cells and has been shown to induce angiogenesis and endothelial cell migration through stimulation of endothelial tyrosine-kinase receptors. Here, using confocal microscopy and the patch-clamp technique on endothelial cells, membrane permeability to calcium as well as cytoplasmic and nuclear free calcium levels have been investigated in the first stages of tyrosine-kinase receptor activation by VEGF. VEGF (0.5nM) as well as inositol trisphosphate (IP3) induced an activation of membrane calcium-permeable channels exhibiting a similar low conductance in the range of 10 pS. The VEGF-triggered activation of these calcium channels, mediated by IP3 and involving the intracellular calcium stores, results in an increase in both cytoplasmic and nuclear calcium levels in endothelial cells, potentially modulating gene expression. Finally, the effect of Ni2+, a calcium channel blocker, on endothelial cell proliferation has been studied. The results show that inhibition of extracellular calcium influx significantly inhibits VEGF-induced cell proliferation. In the process of cell stimulation by VEGF, and possibly by other growth factors, activation of calcium channels could then be a key step in calcium-regulated gene expression and cell activation. These results suggest that the use of calcium channel blockers could be a novel way of prevention or reversion of VEGF-induced tumoral angiogenesis.
Databáze: OpenAIRE