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dc.contributor.authorGenes, Nicholas G.
dc.contributor.authorRowley, Jon A.
dc.contributor.authorMooney, David J.
dc.contributor.authorBonassar, Lawrence J.
dc.date2022-08-11T08:08:57.000
dc.date.accessioned2022-08-23T16:13:53Z
dc.date.available2022-08-23T16:13:53Z
dc.date.issued2004-02-05
dc.date.submitted2008-09-11
dc.identifier.citationArch Biochem Biophys. 2004 Feb 15;422(2):161-7. <a href="http://dx.doi.org/10.1016/j.abb.2003.11.023">Link to article on publisher's site</a>
dc.identifier.issn0003-9861 (Print)
dc.identifier.doi10.1016/j.abb.2003.11.023
dc.identifier.pmid14759603
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33730
dc.description.abstractThis study characterized the attachment of chondrocytes to RGD-functionalized alginate by examining the effect of substrate stiffness on cell attachment and morphology. Bovine chondrocytes were added to wells coated with 2% alginate or RGD-alginate. The alginate was crosslinked with divalent cations ranging from 1.25 to 62.5 mmol/g alginate. Attachment to RGD-alginate was 10-20 times higher than attachment to unmodified alginate and was significantly inhibited by antibodies to integrin subunits alpha3l and beta1, cytochalasin-D, and soluble RGD peptide. The equilibrium level and rate of attachment increased with crosslink density and substrate stiffness. Substrate stiffness also regulated chondrocyte morphology, which changed from a rounded shape with nebulous actin on weaker substrates to a predominantly flat morphology with actin stress fibers on stiffer substrates. The dependence of attachment on integrins and substrate stiffness suggests that chondrocyte integrins may play a role in sensing the mechanical properties of the matrices to which they are attached.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=14759603&dopt=Abstract ">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.abb.2003.11.023
dc.subjectAlginates; Amino Acid Sequence; Animals; Barium; Biocompatible Materials; Calcium; Cattle; Cell Adhesion; Chondrocytes; Cross-Linking Reagents; Cytochalasin D; Dose-Response Relationship, Drug; Kinetics; Microscopy, Electron, Scanning; Oligopeptides; Surface Properties
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleEffect of substrate mechanics on chondrocyte adhesion to modified alginate surfaces
dc.typeJournal Article
dc.source.journaltitleArchives of biochemistry and biophysics
dc.source.volume422
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/393
dc.identifier.contextkey627230
html.description.abstract<p>This study characterized the attachment of chondrocytes to RGD-functionalized alginate by examining the effect of substrate stiffness on cell attachment and morphology. Bovine chondrocytes were added to wells coated with 2% alginate or RGD-alginate. The alginate was crosslinked with divalent cations ranging from 1.25 to 62.5 mmol/g alginate. Attachment to RGD-alginate was 10-20 times higher than attachment to unmodified alginate and was significantly inhibited by antibodies to integrin subunits alpha3l and beta1, cytochalasin-D, and soluble RGD peptide. The equilibrium level and rate of attachment increased with crosslink density and substrate stiffness. Substrate stiffness also regulated chondrocyte morphology, which changed from a rounded shape with nebulous actin on weaker substrates to a predominantly flat morphology with actin stress fibers on stiffer substrates. The dependence of attachment on integrins and substrate stiffness suggests that chondrocyte integrins may play a role in sensing the mechanical properties of the matrices to which they are attached.</p>
dc.identifier.submissionpathgsbs_sp/393
dc.contributor.departmentCenter for Tissue Engineering
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages161-7


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