Effect of substrate mechanics on chondrocyte adhesion to modified alginate surfaces
| dc.contributor.author | Genes, Nicholas G. | |
| dc.contributor.author | Rowley, Jon A. | |
| dc.contributor.author | Mooney, David J. | |
| dc.contributor.author | Bonassar, Lawrence J. | |
| dc.date | 2022-08-11T08:08:57.000 | |
| dc.date.accessioned | 2022-08-23T16:13:53Z | |
| dc.date.available | 2022-08-23T16:13:53Z | |
| dc.date.issued | 2004-02-05 | |
| dc.date.submitted | 2008-09-11 | |
| dc.identifier.citation | Arch 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.issn | 0003-9861 (Print) | |
| dc.identifier.doi | 10.1016/j.abb.2003.11.023 | |
| dc.identifier.pmid | 14759603 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14038/33730 | |
| dc.description.abstract | 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. | |
| dc.language.iso | en_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.url | http://dx.doi.org/10.1016/j.abb.2003.11.023 | |
| dc.subject | Alginates; 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.subject | Life Sciences | |
| dc.subject | Medicine and Health Sciences | |
| dc.title | Effect of substrate mechanics on chondrocyte adhesion to modified alginate surfaces | |
| dc.type | Journal Article | |
| dc.source.journaltitle | Archives of biochemistry and biophysics | |
| dc.source.volume | 422 | |
| dc.source.issue | 2 | |
| dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/gsbs_sp/393 | |
| dc.identifier.contextkey | 627230 | |
| 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.submissionpath | gsbs_sp/393 | |
| dc.contributor.department | Center for Tissue Engineering | |
| dc.contributor.department | Graduate School of Biomedical Sciences | |
| dc.source.pages | 161-7 |