Effect of Co-presentation of Adhesive Ligands and Short Hyaluronan on Lymphendothelial Cells

Controlled activation of lymphangiogenesis through functional biomaterials represents a promising approach to support wound healing after surgical procedures, yet remains a challenge. In a synthetic biological approach, we therefore set out to mimic the basal microenvironment of human primary dermal...

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Main Authors: Christiane H. Antoni, Yvonne McDuffie, Jochen Bauer, Jonathan P. Sleeman, Heike Boehm
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fbioe.2018.00025/full
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author Christiane H. Antoni
Christiane H. Antoni
Yvonne McDuffie
Yvonne McDuffie
Jochen Bauer
Jonathan P. Sleeman
Jonathan P. Sleeman
Heike Boehm
Heike Boehm
author_facet Christiane H. Antoni
Christiane H. Antoni
Yvonne McDuffie
Yvonne McDuffie
Jochen Bauer
Jonathan P. Sleeman
Jonathan P. Sleeman
Heike Boehm
Heike Boehm
author_sort Christiane H. Antoni
collection DOAJ
description Controlled activation of lymphangiogenesis through functional biomaterials represents a promising approach to support wound healing after surgical procedures, yet remains a challenge. In a synthetic biological approach, we therefore set out to mimic the basal microenvironment of human primary dermal lymphatic endothelial cells (LECs) during lymphangiogenesis. As the extracellular matrix component hyaluronan (HA) regulates lymphangiogenesis, we designed a bifunctional surface in which adhesive peptide ligands and short HA oligosaccharides (sHA) tethered to nanoparticles are copresented to the basal side of LECs in a controlled, concentration-dependent manner. Exposure of LECs to sHA in solution to mimic luminal stimulation of the cells did not result in modified metabolic activity. However, LECs grown on the bifunctional adhesive surfaces showed a biphasic change in metabolic activity, with increased metabolic activity being observed in response to increasing nanoparticle densities up to a maximum of 540 particles/μm2. Thus, interfaces that concomitantly present adhesive ligands and sHA can stimulate LEC metabolism and might be able to trigger lymphangiogenesis.
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spelling doaj.art-90e60a7cb34441288079b0da794cc98b2022-12-22T00:00:45ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852018-03-01610.3389/fbioe.2018.00025340682Effect of Co-presentation of Adhesive Ligands and Short Hyaluronan on Lymphendothelial CellsChristiane H. Antoni0Christiane H. Antoni1Yvonne McDuffie2Yvonne McDuffie3Jochen Bauer4Jonathan P. Sleeman5Jonathan P. Sleeman6Heike Boehm7Heike Boehm8Department of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg, GermanyDepartment of Biophysical Chemistry, University of Heidelberg, Heidelberg, GermanyDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg, GermanyDepartment of Biophysical Chemistry, University of Heidelberg, Heidelberg, GermanyInstitute of Toxicology and Genetics, Karlsruhe Institute for Technology (KIT), Karlsruhe, GermanyInstitute of Toxicology and Genetics, Karlsruhe Institute for Technology (KIT), Karlsruhe, GermanyMedical Faculty Mannheim, University of Heidelberg, Mannheim, GermanyDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg, GermanyDepartment of Biophysical Chemistry, University of Heidelberg, Heidelberg, GermanyControlled activation of lymphangiogenesis through functional biomaterials represents a promising approach to support wound healing after surgical procedures, yet remains a challenge. In a synthetic biological approach, we therefore set out to mimic the basal microenvironment of human primary dermal lymphatic endothelial cells (LECs) during lymphangiogenesis. As the extracellular matrix component hyaluronan (HA) regulates lymphangiogenesis, we designed a bifunctional surface in which adhesive peptide ligands and short HA oligosaccharides (sHA) tethered to nanoparticles are copresented to the basal side of LECs in a controlled, concentration-dependent manner. Exposure of LECs to sHA in solution to mimic luminal stimulation of the cells did not result in modified metabolic activity. However, LECs grown on the bifunctional adhesive surfaces showed a biphasic change in metabolic activity, with increased metabolic activity being observed in response to increasing nanoparticle densities up to a maximum of 540 particles/μm2. Thus, interfaces that concomitantly present adhesive ligands and sHA can stimulate LEC metabolism and might be able to trigger lymphangiogenesis.http://journal.frontiersin.org/article/10.3389/fbioe.2018.00025/fullhyaluronanlymphangiogenesisextracellular matrix mimeticlymphendothelial cellsbioactive interface
spellingShingle Christiane H. Antoni
Christiane H. Antoni
Yvonne McDuffie
Yvonne McDuffie
Jochen Bauer
Jonathan P. Sleeman
Jonathan P. Sleeman
Heike Boehm
Heike Boehm
Effect of Co-presentation of Adhesive Ligands and Short Hyaluronan on Lymphendothelial Cells
Frontiers in Bioengineering and Biotechnology
hyaluronan
lymphangiogenesis
extracellular matrix mimetic
lymphendothelial cells
bioactive interface
title Effect of Co-presentation of Adhesive Ligands and Short Hyaluronan on Lymphendothelial Cells
title_full Effect of Co-presentation of Adhesive Ligands and Short Hyaluronan on Lymphendothelial Cells
title_fullStr Effect of Co-presentation of Adhesive Ligands and Short Hyaluronan on Lymphendothelial Cells
title_full_unstemmed Effect of Co-presentation of Adhesive Ligands and Short Hyaluronan on Lymphendothelial Cells
title_short Effect of Co-presentation of Adhesive Ligands and Short Hyaluronan on Lymphendothelial Cells
title_sort effect of co presentation of adhesive ligands and short hyaluronan on lymphendothelial cells
topic hyaluronan
lymphangiogenesis
extracellular matrix mimetic
lymphendothelial cells
bioactive interface
url http://journal.frontiersin.org/article/10.3389/fbioe.2018.00025/full
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