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BiomaterialsVolume 32, Issue 31, November 2011, Pages 7897-7904

Injectable in situ crosslinkable RGD-modified alginate matrix for endothelial cells delivery(Article)

  • aINEB - Instituto de Engenharia Biomédica, Rua do Campo Alegre n 823, 4150-180 Porto, Portugal
  • bFEUP - Faculty of Engineering, Universidade do Porto, Rua Dr Roberto Frias s/n, 4200- 465 Porto, Portugal
  • cDepartment of Biochemistry (U38), Faculty of Medicine, Universidade do Porto, Portugal

Abstract

Cell-based therapies offer an attractive approach for revascularization and regeneration of tissues. However, and despite the pressing clinical needs for effective revascularization strategies, the successful immobilization of viable vascular cells within 3D matrices has been difficult to achieve. In this paper the in vitro potential of a natural, injectable RGD-alginate hydrogel as an in situ forming matrix to deliver endothelial cells was evaluated. Several techniques were employed to investigate how these microenvironments could influence the behavior of vascular cells, namely their ability to promote the outward migration of viable, proliferative cells, retaining the ability to form a 3D arrangement. Cells within RGD-grafted alginate hydrogel were able to proliferate and maintained 80% of viability for at least 48 h post-immobilization. Additionally, entrapped cells created a 3D organization into cellular networks and, when put in contact with matrigel, cells migrated out of the RGD-matrix. Overall, the obtained results support the idea that the RGD peptides conjugated to alginate provide a 3D environment for endothelial cells adhesion, survival, migration and organization. © 2011 Elsevier Ltd.

Author keywords

AlginateCell adhesionEndothelial cellRGD peptideScaffold

Indexed keywords

Engineering uncontrolled terms3-D environmentsAlginate hydrogelsAlginate matrixCell-based therapyCellular networkCross-linkableIn-situIn-situ formingIn-vitromatrixMicroenvironmentsProliferative cellsRevascularizationRGD peptideVascular cells
Engineering controlled terms:AdhesionAlginateCell adhesionCell immobilizationCell proliferationCellular neural networksHydrogelsPeptidesScaffolds (biology)Three dimensionalTissue
Engineering main heading:Endothelial cells
EMTREE drug terms:alginic acidangiopoietin 2arginylglycylaspartic acidmatrigelmessenger RNAmolecular scaffoldvon Willebrand factor
EMTREE medical terms:articlecell adhesioncell migrationcell proliferationcell structurecell survivalcell transportcell viabilitycross linkingendothelium cellextracellular matrixgene expressionhumanhuman cellhydrogelimmobilized cellimmunofluorescencein situ crosslinkingin vitro studymicroenvironmentphenotypepriority journalumbilical vein endothelial cell
MeSH:AlginatesAngiopoietin-2Cell MovementCell ProliferationCell ShapeCell SurvivalCells, CulturedCross-Linking ReagentsExtracellular MatrixFluoresceinsHuman Umbilical Vein Endothelial CellsHumansHydrogelsInjectionsMatrix MetalloproteinasesOligopeptidesSolutionsSuccinimides

Chemicals and CAS Registry Numbers:

alginic acid, 28961-37-7, 29894-36-8, 9005-32-7, 9005-38-3; angiopoietin 2, 194368-66-6; arginylglycylaspartic acid, 99896-85-2; matrigel, 119978-18-6; von Willebrand factor, 109319-16-6;

5-(6)-carboxyfluorescein diacetate succinimidyl ester; Alginates; Angiopoietin-2; Cross-Linking Reagents; Fluoresceins; Hydrogels; Matrix Metalloproteinases, 3.4.24.-; Oligopeptides; Solutions; Succinimides; arginyl-glycyl-aspartic acid, 99896-85-2

Funding details

Funding sponsor Funding number Acronym
Fuel Cell Technologies ProgramPOCTI/SAU-BMA/55556/2004,FCOMP-01-0124-FEDER-010915,SFRH/BD/22307/2005,PTDC/SAU-BEB/101235/2008FCT
  • 1

    The authors are grateful to the Portuguese Foundation for Science and Technology (FCT) for awarding S.J. Bidarra a scholarship SFRH/BD/22307/2005. This work was carried out under contract POCTI/SAU-BMA/55556/2004 and PTDC/SAU-BEB/101235/2008 and FCOMP-01-0124-FEDER-010915.

  • ISSN: 01429612
  • CODEN: BIMAD
  • Source Type: Journal
  • Original language: English
  • DOI: 10.1016/j.biomaterials.2011.07.013
  • PubMed ID: 21784515
  • Document Type: Article

  Granja, P.L.; INEB-Instituto de Engenharia Biomédica, Rua do Campo Alegre, n 823, Portugal;
© Copyright 2012 Elsevier B.V., All rights reserved. © MEDLINE® is the source for the MeSH terms of this document.

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