A phosphoinositide 3-kinase/phospholipase cgamma1 pathway regulates fibroblast growth factor-induced capillary tube formation

Background: The fibroblast growth factors (FGFs) are key regulators of embryonic development, tissue homeostasis and tumour angiogenesis. Binding of FGFs to their receptor(s) results in activation of several intracellular signalling cascades including phosphoinositide 3-kinase (PI3K) and phospholipa...

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Main Authors: Maffucci, T., Raimondi, C., Abu-Hayyeh, S., Dominguez, V., Sala, G., Zachary, I., Falasca, Marco
Format: Journal Article
Published: Public Library of Science 2009
Online Access:http://hdl.handle.net/20.500.11937/40432
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author Maffucci, T.
Raimondi, C.
Abu-Hayyeh, S.
Dominguez, V.
Sala, G.
Zachary, I.
Falasca, Marco
author_facet Maffucci, T.
Raimondi, C.
Abu-Hayyeh, S.
Dominguez, V.
Sala, G.
Zachary, I.
Falasca, Marco
author_sort Maffucci, T.
building Curtin Institutional Repository
collection Online Access
description Background: The fibroblast growth factors (FGFs) are key regulators of embryonic development, tissue homeostasis and tumour angiogenesis. Binding of FGFs to their receptor(s) results in activation of several intracellular signalling cascades including phosphoinositide 3-kinase (PI3K) and phospholipase C (PLC)?1. Here we investigated the basic FGF (FGF-2)-mediated activation of these enzymes in human umbilical vein endothelial cells (HUVECs) and defined their role in FGF-2-dependent cellular functions. Methodology/Principal Findings: We show that FGF-2 activates PLC?1 in HUVECs measured by analysis of total inositol phosphates production upon metabolic labelling of cells and intracellular calcium increase. We further demonstrate that FGF-2 activates PI3K, assessed by analysing accumulation of its lipid product phosphatidylinositol-3,4,5-P3 using TLC and confocal microscopy analysis. PI3K activity is required for FGF-2-induced PLCc1 activation and the PI3K/PLCc1 pathway is involved in FGF-2-dependent cell migration, determined using Transwell assay, and in FGF-2-induced capillary tube formation (tubulogenesis assays in vitro). Finally we show that PI3K-dependent PLC?1 activation regulates FGF-2-mediated phosphorylation of Akt at its residue Ser473, determined by Western blotting analysis. This occurs through protein kinase C (PKC)a activation since dowregulation of PKCa expression using specific siRNA or blockade of its activity using chemical inhibition affects the FGF-2-dependent Ser473 Akt phosphorylation. Furthermore inhibition of PKCa blocks FGF-2-dependent cell migration. Conclusion/Significance: These data elucidate the role of PLC?1 in FGF-2 signalling in HUVECs demonstrating its key role in FGF-2-dependent tubulogenesis. Furthermore these data unveil a novel role for PLC?1 as a mediator of PI3K-dependent Akt activation and as a novel key regulator of different Akt-dependent processes. a 2009 Maffucci et al.
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institution Curtin University Malaysia
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last_indexed 2025-11-14T09:03:10Z
publishDate 2009
publisher Public Library of Science
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spelling curtin-20.500.11937-404322017-09-13T13:38:56Z A phosphoinositide 3-kinase/phospholipase cgamma1 pathway regulates fibroblast growth factor-induced capillary tube formation Maffucci, T. Raimondi, C. Abu-Hayyeh, S. Dominguez, V. Sala, G. Zachary, I. Falasca, Marco Background: The fibroblast growth factors (FGFs) are key regulators of embryonic development, tissue homeostasis and tumour angiogenesis. Binding of FGFs to their receptor(s) results in activation of several intracellular signalling cascades including phosphoinositide 3-kinase (PI3K) and phospholipase C (PLC)?1. Here we investigated the basic FGF (FGF-2)-mediated activation of these enzymes in human umbilical vein endothelial cells (HUVECs) and defined their role in FGF-2-dependent cellular functions. Methodology/Principal Findings: We show that FGF-2 activates PLC?1 in HUVECs measured by analysis of total inositol phosphates production upon metabolic labelling of cells and intracellular calcium increase. We further demonstrate that FGF-2 activates PI3K, assessed by analysing accumulation of its lipid product phosphatidylinositol-3,4,5-P3 using TLC and confocal microscopy analysis. PI3K activity is required for FGF-2-induced PLCc1 activation and the PI3K/PLCc1 pathway is involved in FGF-2-dependent cell migration, determined using Transwell assay, and in FGF-2-induced capillary tube formation (tubulogenesis assays in vitro). Finally we show that PI3K-dependent PLC?1 activation regulates FGF-2-mediated phosphorylation of Akt at its residue Ser473, determined by Western blotting analysis. This occurs through protein kinase C (PKC)a activation since dowregulation of PKCa expression using specific siRNA or blockade of its activity using chemical inhibition affects the FGF-2-dependent Ser473 Akt phosphorylation. Furthermore inhibition of PKCa blocks FGF-2-dependent cell migration. Conclusion/Significance: These data elucidate the role of PLC?1 in FGF-2 signalling in HUVECs demonstrating its key role in FGF-2-dependent tubulogenesis. Furthermore these data unveil a novel role for PLC?1 as a mediator of PI3K-dependent Akt activation and as a novel key regulator of different Akt-dependent processes. a 2009 Maffucci et al. 2009 Journal Article http://hdl.handle.net/20.500.11937/40432 10.1371/journal.pone.0008285 Public Library of Science unknown
spellingShingle Maffucci, T.
Raimondi, C.
Abu-Hayyeh, S.
Dominguez, V.
Sala, G.
Zachary, I.
Falasca, Marco
A phosphoinositide 3-kinase/phospholipase cgamma1 pathway regulates fibroblast growth factor-induced capillary tube formation
title A phosphoinositide 3-kinase/phospholipase cgamma1 pathway regulates fibroblast growth factor-induced capillary tube formation
title_full A phosphoinositide 3-kinase/phospholipase cgamma1 pathway regulates fibroblast growth factor-induced capillary tube formation
title_fullStr A phosphoinositide 3-kinase/phospholipase cgamma1 pathway regulates fibroblast growth factor-induced capillary tube formation
title_full_unstemmed A phosphoinositide 3-kinase/phospholipase cgamma1 pathway regulates fibroblast growth factor-induced capillary tube formation
title_short A phosphoinositide 3-kinase/phospholipase cgamma1 pathway regulates fibroblast growth factor-induced capillary tube formation
title_sort phosphoinositide 3-kinase/phospholipase cgamma1 pathway regulates fibroblast growth factor-induced capillary tube formation
url http://hdl.handle.net/20.500.11937/40432