Polysialic acid is released by human umbilical vein endothelial cells (HUVEC) in vitro

Abstract Background Sialic acids represent common terminal residues on numerous mammalian glycoconjugates, thereby influencing e.g. lumen formation in developing blood vessels. Interestingly, besides monosialylated also polysialylated glycoconjugates are produced by endothelial cells. Polysialic aci...

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Main Authors: Sebastian Strubl, Uwe Schubert, Andrea Kühnle, Alexander Rebl, Negah Ahmadvand, Silvia Fischer, Klaus T. Preissner, Sebastian P. Galuska
Format: Article
Language:English
Published: BMC 2018-12-01
Series:Cell & Bioscience
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13578-018-0262-y
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author Sebastian Strubl
Uwe Schubert
Andrea Kühnle
Alexander Rebl
Negah Ahmadvand
Silvia Fischer
Klaus T. Preissner
Sebastian P. Galuska
author_facet Sebastian Strubl
Uwe Schubert
Andrea Kühnle
Alexander Rebl
Negah Ahmadvand
Silvia Fischer
Klaus T. Preissner
Sebastian P. Galuska
author_sort Sebastian Strubl
collection DOAJ
description Abstract Background Sialic acids represent common terminal residues on numerous mammalian glycoconjugates, thereby influencing e.g. lumen formation in developing blood vessels. Interestingly, besides monosialylated also polysialylated glycoconjugates are produced by endothelial cells. Polysialic acid (polySia) is formed in several organs during embryonal and postnatal development influencing, for instance, cell migration processes. Furthermore, the function of cytokines like basic fibroblast growth factor (bFGF) is modulated by polySia. Results In this study, we demonstrated that human umbilical vein endothelial cells (HUVEC) also secrete polysialylated glycoconjugates. Furthermore, an interaction between polySia and vascular endothelial growth factor (VEGF) was observed. VEGF modulates like bFGF the migration of HUVEC. Since both growth factors interact with polySia, we examined, if polySia modulates the migration of HUVEC. To this end scratch assays were performed showing that the migration of HUVEC is stimulated, when polySia was degraded. Conclusions Since polySia can interact with bFGF as well as VEGF and the degradation of polySia resulted in an increased cell migration capacity in the applied scratch assay, we propose that polySia may trap these growth factors influencing their biological activity. Thus, polySia might also contribute to the fine regulation of physiological processes in endothelial cells.
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spelling doaj.art-d193c312727b4b15ae95bce8147d42b92022-12-22T00:02:15ZengBMCCell & Bioscience2045-37012018-12-01811910.1186/s13578-018-0262-yPolysialic acid is released by human umbilical vein endothelial cells (HUVEC) in vitroSebastian Strubl0Uwe Schubert1Andrea Kühnle2Alexander Rebl3Negah Ahmadvand4Silvia Fischer5Klaus T. Preissner6Sebastian P. Galuska7Institute of Biochemistry, Faculty of Medicine, Justus-Liebig-UniversityInstitute of Biochemistry, Faculty of Medicine, Justus-Liebig-UniversityInstitute of Reproductive Biology, Leibniz Institute for Farm Animal Biology (FBN)Institute of Genome Biology, Leibniz Institute for Farm Animal Biology (FBN)Institute of Biochemistry, Faculty of Medicine, Justus-Liebig-UniversityInstitute of Biochemistry, Faculty of Medicine, Justus-Liebig-UniversityInstitute of Biochemistry, Faculty of Medicine, Justus-Liebig-UniversityInstitute of Biochemistry, Faculty of Medicine, Justus-Liebig-UniversityAbstract Background Sialic acids represent common terminal residues on numerous mammalian glycoconjugates, thereby influencing e.g. lumen formation in developing blood vessels. Interestingly, besides monosialylated also polysialylated glycoconjugates are produced by endothelial cells. Polysialic acid (polySia) is formed in several organs during embryonal and postnatal development influencing, for instance, cell migration processes. Furthermore, the function of cytokines like basic fibroblast growth factor (bFGF) is modulated by polySia. Results In this study, we demonstrated that human umbilical vein endothelial cells (HUVEC) also secrete polysialylated glycoconjugates. Furthermore, an interaction between polySia and vascular endothelial growth factor (VEGF) was observed. VEGF modulates like bFGF the migration of HUVEC. Since both growth factors interact with polySia, we examined, if polySia modulates the migration of HUVEC. To this end scratch assays were performed showing that the migration of HUVEC is stimulated, when polySia was degraded. Conclusions Since polySia can interact with bFGF as well as VEGF and the degradation of polySia resulted in an increased cell migration capacity in the applied scratch assay, we propose that polySia may trap these growth factors influencing their biological activity. Thus, polySia might also contribute to the fine regulation of physiological processes in endothelial cells.http://link.springer.com/article/10.1186/s13578-018-0262-yHuman umbilical vein endothelial cellsPolysialic acidVascular endothelial growth factor
spellingShingle Sebastian Strubl
Uwe Schubert
Andrea Kühnle
Alexander Rebl
Negah Ahmadvand
Silvia Fischer
Klaus T. Preissner
Sebastian P. Galuska
Polysialic acid is released by human umbilical vein endothelial cells (HUVEC) in vitro
Cell & Bioscience
Human umbilical vein endothelial cells
Polysialic acid
Vascular endothelial growth factor
title Polysialic acid is released by human umbilical vein endothelial cells (HUVEC) in vitro
title_full Polysialic acid is released by human umbilical vein endothelial cells (HUVEC) in vitro
title_fullStr Polysialic acid is released by human umbilical vein endothelial cells (HUVEC) in vitro
title_full_unstemmed Polysialic acid is released by human umbilical vein endothelial cells (HUVEC) in vitro
title_short Polysialic acid is released by human umbilical vein endothelial cells (HUVEC) in vitro
title_sort polysialic acid is released by human umbilical vein endothelial cells huvec in vitro
topic Human umbilical vein endothelial cells
Polysialic acid
Vascular endothelial growth factor
url http://link.springer.com/article/10.1186/s13578-018-0262-y
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