Immobilization of Cell-Adhesive Laminin Peptides in Degradable PEGDA Hydrogels Influences Endothelial Cell Tubulogenesis

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dc.citation.journalTitleBioResearch Open Accessen_US
dc.contributor.authorAli, Saniyaen_US
dc.contributor.authorSaik, Jennifer E.en_US
dc.contributor.authorGould, Dan J.en_US
dc.contributor.authorDickinson, Mary E.en_US
dc.contributor.authorWest, Jennifer L.en_US
dc.date.accessioned2013-06-19T18:03:48Zen_US
dc.date.available2013-06-19T18:03:48Zen_US
dc.date.issued2013en_US
dc.description.abstractAttachment, spreading, and organization of endothelial cells into tubule networks are mediated by interactions between cells in the extracellular microenvironment. Laminins are key extracellular matrix components and regulators of cell adhesion, migration, and proliferation. In this study, laminin-derived peptides were conjugated to poly(ethylene glycol) (PEG) monoacrylate and covalently incorporated into degradable PEG diacrylate (PEGDA) hydrogels to investigate the influence of these peptides on endothelial cellular adhesion and function in organizing into tubule networks. Degradable PEGDA hydrogels were synthesized by incorporating a matrix metalloproteinase (MMP)-sensitive peptide, GGGPQGIWGQGK (abbreviated PQ), into the polymer backbone. The secretion ofMMP-2 and MMP-9 by endothelial cells promotes polymer degradation and consequently cell migration. We demonstrate the formation of extensive networks of tubule-like structures by encapsulated human umbilical vein endothelial cells in hydrogels with immobilized synthetic peptides. The resulting structures were stabilized by pericyte precursor cells (10T1/2s) in vitro. During tubule formation and stabilization, extracellular matrix proteins such as collagen IV and laminin were deposited. Tubules formed in the matrix of metalloproteinase sensitive hydrogels were visualized from 7 days to 4 weeks in response to different combination of peptides. Moreover, hydrogels functionalized with laminin peptides and transplanted in a mouse cornea supported the ingrowth and attachment of endothelial cells to the hydrogel during angiogenesis. Results of this study illustrate the use of laminin-derived peptides as potential candidates for modification of biomaterials to support angiogenesis.en_US
dc.embargo.termsnoneen_US
dc.identifier.citationAli, Saniya, Saik, Jennifer E., Gould, Dan J., et al.. "Immobilization of Cell-Adhesive Laminin Peptides in Degradable PEGDA Hydrogels Influences Endothelial Cell Tubulogenesis." <i>BioResearch Open Access,</i> (2013) Mary Ann Liebert, Inc.: http://dx.doi.org/10.1089/biores.2013.0021.en_US
dc.identifier.doihttp://dx.doi.org/10.1089/biores.2013.0021en_US
dc.identifier.urihttps://hdl.handle.net/1911/71332en_US
dc.language.isoengen_US
dc.publisherMary Ann Liebert, Inc.en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.subject.keywordangiogenesisen_US
dc.subject.keywordbiomaterialsen_US
dc.subject.keywordextracellular matrixen_US
dc.subject.keywordpeptidesen_US
dc.subject.keywordtissue engineeringen_US
dc.titleImmobilization of Cell-Adhesive Laminin Peptides in Degradable PEGDA Hydrogels Influences Endothelial Cell Tubulogenesisen_US
dc.typeJournal articleen_US
dc.type.dcmiTexten_US
dc.type.publicationpublisher versionen_US
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