Low-molecular-weight fucoidan enhances the proangiogenic phenotype of endothelial progenitor cells
Endothelial progenitor cell (EPC) transplantation is a potential means of inducing neovascularization in vivo. However, the number of circulating EPC is relatively small, it may thus be necessary to enhance their proangiogenic properties ex vivo prior to injection in vivo. Fucoidan has previously be...
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Published in | Biochemical pharmacology Vol. 70; no. 8; pp. 1167 - 1175 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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New York, NY
Elsevier Inc
15.10.2005
Elsevier Science |
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Abstract | Endothelial progenitor cell (EPC) transplantation is a potential means of inducing neovascularization in vivo. However, the number of circulating EPC is relatively small, it may thus be necessary to enhance their proangiogenic properties ex vivo prior to injection in vivo. Fucoidan has previously been shown to potentiate in vitro tube formation by mature endothelial cells in the presence of basic fibroblast growth factor (FGF-2). We therefore examined whether fucoidan, alone or combined with FGF-2, could increase EPC proangiogenic potency in vitro. EPC exposure to 10
μg/ml fucoidan induced a proangiogenic phenotype, including cell proliferation (
p
<
0.01) and migration (
p
<
0.01); moreover, differentiation into vascular cords occurred in the presence of FGF-2 (
p
<
0.01). This latter effect correlated with upregulation of the cell-surface #α6 integrin subunit of the laminin receptor (
p
<
0.05). Compared to untreated HUVEC, untreated EPC #α6 expression and adhesion to laminin were enhanced two-fold. Fucoidan treatment further enhanced HUVEC but not EPC adhesion to laminin. These results show that fucoidan enhances the proangiogenic properties of EPC and suggest that ex vivo fucoidan preconditioning of EPC might lead to increased neovascularization when injected into ischemic tissues. |
---|---|
AbstractList | Endothelial progenitor cell (EPC) transplantation is a potential means of inducing neovascularization in vivo. However, the number of circulating EPC is relatively small, it may thus be necessary to enhance their proangiogenic properties ex vivo prior to injection in vivo. Fucoidan has previously been shown to potentiate in vitro tube formation by mature endothelial cells in the presence of basic fibroblast growth factor (FGF-2). We therefore examined whether fucoidan, alone or combined with FGF-2, could increase EPC proangiogenic potency in vitro. EPC exposure to 10
μg/ml fucoidan induced a proangiogenic phenotype, including cell proliferation (
p
<
0.01) and migration (
p
<
0.01); moreover, differentiation into vascular cords occurred in the presence of FGF-2 (
p
<
0.01). This latter effect correlated with upregulation of the cell-surface #α6 integrin subunit of the laminin receptor (
p
<
0.05). Compared to untreated HUVEC, untreated EPC #α6 expression and adhesion to laminin were enhanced two-fold. Fucoidan treatment further enhanced HUVEC but not EPC adhesion to laminin. These results show that fucoidan enhances the proangiogenic properties of EPC and suggest that ex vivo fucoidan preconditioning of EPC might lead to increased neovascularization when injected into ischemic tissues. Endothelial progenitor cell (EPC) transplantation is a potential means of inducing neovascularization in vivo. However, the number of circulating EPC is relatively small, it may thus be necessary to enhance their proangiogenic properties ex vivo prior to injection in vivo. Fucoidan has previously been shown to potentiate in vitro tube formation by mature endothelial cells in the presence of basic fibroblast growth factor (FGF-2). We therefore examined whether fucoidan, alone or combined with FGF-2, could increase EPC proangiogenic potency in vitro. EPC exposure to 10 microg/ml fucoidan induced a proangiogenic phenotype, including cell proliferation (p < 0.01) and migration (p < 0.01); moreover, differentiation into vascular cords occurred in the presence of FGF-2 (p < 0.01). This latter effect correlated with upregulation of the cell-surface #alpha6 integrin subunit of the laminin receptor (p < 0.05). Compared to untreated HUVEC, untreated EPC #alpha6 expression and adhesion to laminin were enhanced two-fold. Fucoidan treatment further enhanced HUVEC but not EPC adhesion to laminin. These results show that fucoidan enhances the proangiogenic properties of EPC and suggest that ex vivo fucoidan preconditioning of EPC might lead to increased neovascularization when injected into ischemic tissues. Endothelial progenitor cell (EPC) transplantation is a potential means of inducing neovascularization in vivo. However, the number of circulating EPC is relatively small, it may thus be necessary to enhance their proangiogenic properties ex vivo prior to injection in vivo. Fucoidan has previously been shown to potentiate in vitro tube formation by mature endothelial cells in the presence of basic fibroblast growth factor (FGF-2). We therefore examined whether fucoidan, alone or combined with FGF-2, could increase EPC proangiogenic potency in vitro. EPC exposure to 10 microg/ml fucoidan induced a proangiogenic phenotype, including cell proliferation (p < 0.01) and migration (p < 0.01); moreover, differentiation into vascular cords occurred in the presence of FGF-2 (p < 0.01). This latter effect correlated with upregulation of the cell-surface #alpha6 integrin subunit of the laminin receptor (p < 0.05). Compared to untreated HUVEC, untreated EPC #alpha6 expression and adhesion to laminin were enhanced two-fold. Fucoidan treatment further enhanced HUVEC but not EPC adhesion to laminin. These results show that fucoidan enhances the proangiogenic properties of EPC and suggest that ex vivo fucoidan preconditioning of EPC might lead to increased neovascularization when injected into ischemic tissues.Endothelial progenitor cell (EPC) transplantation is a potential means of inducing neovascularization in vivo. However, the number of circulating EPC is relatively small, it may thus be necessary to enhance their proangiogenic properties ex vivo prior to injection in vivo. Fucoidan has previously been shown to potentiate in vitro tube formation by mature endothelial cells in the presence of basic fibroblast growth factor (FGF-2). We therefore examined whether fucoidan, alone or combined with FGF-2, could increase EPC proangiogenic potency in vitro. EPC exposure to 10 microg/ml fucoidan induced a proangiogenic phenotype, including cell proliferation (p < 0.01) and migration (p < 0.01); moreover, differentiation into vascular cords occurred in the presence of FGF-2 (p < 0.01). This latter effect correlated with upregulation of the cell-surface #alpha6 integrin subunit of the laminin receptor (p < 0.05). Compared to untreated HUVEC, untreated EPC #alpha6 expression and adhesion to laminin were enhanced two-fold. Fucoidan treatment further enhanced HUVEC but not EPC adhesion to laminin. These results show that fucoidan enhances the proangiogenic properties of EPC and suggest that ex vivo fucoidan preconditioning of EPC might lead to increased neovascularization when injected into ischemic tissues. |
Author | Uzan, Georges Galy-Fauroux, Isabelle Zemani, Faouzia Boisson-Vidal, Catherine Colliec-Jouault, Sylvia Benisvy, Danielle Lokajczyk, Anna Fischer, Anne Marie |
Author_xml | – sequence: 1 givenname: Faouzia surname: Zemani fullname: Zemani, Faouzia organization: INSERM U428, 4 av. de l’Observatoire, Faculté de Pharmacie, 75270 Paris Cedex 06, France – sequence: 2 givenname: Danielle surname: Benisvy fullname: Benisvy, Danielle organization: INSERM U428, 4 av. de l’Observatoire, Faculté de Pharmacie, 75270 Paris Cedex 06, France – sequence: 3 givenname: Isabelle surname: Galy-Fauroux fullname: Galy-Fauroux, Isabelle organization: INSERM U428, 4 av. de l’Observatoire, Faculté de Pharmacie, 75270 Paris Cedex 06, France – sequence: 4 givenname: Anna surname: Lokajczyk fullname: Lokajczyk, Anna organization: INSERM U428, 4 av. de l’Observatoire, Faculté de Pharmacie, 75270 Paris Cedex 06, France – sequence: 5 givenname: Sylvia surname: Colliec-Jouault fullname: Colliec-Jouault, Sylvia organization: IFREMER, Route de l’Ile d’Yeu, Nantes, France – sequence: 6 givenname: Georges surname: Uzan fullname: Uzan, Georges organization: INSERM U506, Hôpital Paul Brousse, Villejuif, France – sequence: 7 givenname: Anne Marie surname: Fischer fullname: Fischer, Anne Marie organization: INSERM U428, 4 av. de l’Observatoire, Faculté de Pharmacie, 75270 Paris Cedex 06, France – sequence: 8 givenname: Catherine surname: Boisson-Vidal fullname: Boisson-Vidal, Catherine email: catherine.boisson-vidal@univ-paris5.fr organization: INSERM U428, 4 av. de l’Observatoire, Faculté de Pharmacie, 75270 Paris Cedex 06, France |
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Keywords | PBS vWF VEGF Alpha #6 FACS Fucoidan ECM FGF-2 Angiogenesis FCS Endothelial progenitor cells KDR EPC HUVEC Endothelial cell Phenotype Stem cell Precursor cell Plant origin Basic fibroblast growth factor Neovascularization Molecular mass Progenitor cell |
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Snippet | Endothelial progenitor cell (EPC) transplantation is a potential means of inducing neovascularization in vivo. However, the number of circulating EPC is... |
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SubjectTerms | Alpha #6 Angiogenesis Biological and medical sciences Cardiovascular system Cell Proliferation Cell Separation Cells, Cultured Endothelial progenitor cells Endothelium - cytology Endothelium - drug effects FGF-2 Fibroblast Growth Factor 2 - metabolism Flow Cytometry Fucoidan Humans Laminin - metabolism Medical sciences Miscellaneous Molecular Weight Neovascularization, Physiologic Pharmacology. Drug treatments Phenotype Polysaccharides - chemistry Polysaccharides - pharmacology Stem Cells - cytology Stem Cells - drug effects |
Title | Low-molecular-weight fucoidan enhances the proangiogenic phenotype of endothelial progenitor cells |
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