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dc.contributor.authorGrodzinsky, Alan J.
dc.contributor.authorWheeler, Cameron A.
dc.contributor.authorJafarzadeh, Seyed R.
dc.contributor.authorRocke, David M.
dc.date.accessioned2011-10-26T17:58:35Z
dc.date.available2011-10-26T17:58:35Z
dc.date.issued2009-02
dc.date.submitted2009-02
dc.identifier.issn1063-4584
dc.identifier.urihttp://hdl.handle.net/1721.1/66590
dc.description.abstractObjective To determine changes in chondrocyte transcription of a range of anabolic, catabolic and signaling genes following simultaneous treatment of cartilage with Insulin-like growth factor-1 (IGF-1) and ramp-and-hold mechanical compression, and compare with effects on biosynthesis. Methods Explant disks of bovine calf cartilage were slowly compressed (unconfined) over 3-min to their 1 mm cut-thickness (0%-compression) or to 50%-compression with or without 300 ng/ml IGF-1. Expression of 24 genes involved in cartilage homeostasis was measured using qPCR at 2, 8, 24, 32, 48 h after compression ±IGF-1. Clustering analysis was used to identify groups of co-expressed genes to further elucidate mechanistic pathways. Results IGF-1 alone stimulated gene expression of aggrecan and collagen II, but simultaneous 24h compression suppressed this effect. Compression alone up-regulated expression of matrix metalloproteinase (MMP)-3, MMP-13, a disintegrin and metalloproteinase with thrombospondin motif (ADAMTS)-5 and transforming growth factor (TGF)-β, an effect not reversed by simultaneous IGF-1 treatment. Temporal changes in expression following IGF-1 treatment were generally slower than that following compression. Clustering analysis revealed five distinct groups within which the pairings, tissue inhibitor of metalloproteinase (TIMP)-3 and ADAMTS-5, MMP-1 and IGF-2, and IGF-1 and Collagen II, were all robustly co-expressed, suggesting inherent regulation and feedback in chondrocyte gene expression. While aggrecan synthesis was transcriptionally regulated by IGF-1, inhibition of aggrecan synthesis by sustained compression appeared post-transcriptionally regulated. Conclusion Sustained compression markedly altered the effects of IGF-1 on expression of genes involved in cartilage homeostasis, while IGF-1 was largely unable to moderate the transcriptional effects of compression alone. The demonstrated co-expressed gene pairings suggest a balance of anabolic and catabolic activity following simultaneous mechanical and growth factor stimuli.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant R01-AR33236)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant R01-HG003352)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant P42-ES04699)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant T32-EB006348)en_US
dc.language.isoen_US
dc.publisherElsevier Ltd.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.joca.2009.02.001en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePubMed Centralen_US
dc.titleIGF-1 does not moderate the time-dependent transcriptional patterns of key homeostatic genes induced by sustained compression of bovine cartilageen_US
dc.typeArticleen_US
dc.identifier.citationWheeler, C.A. et al. “IGF-1 does not moderate the time-dependent transcriptional patterns of key homeostatic genes induced by sustained compression of bovine cartilage.” Osteoarthritis and Cartilage 17 (2009): 944-952. Web. 26 Oct. 2011. © 2009 Elsevier Ltd.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.approverGrodzinsky, Alan J.
dc.contributor.mitauthorGrodzinsky, Alan J.
dc.contributor.mitauthorWheeler, Cameron A.
dc.relation.journalOsteoarthritis and Cartilageen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsWheeler, C.A.; Jafarzadeh, S.R.; Rocke, D.M.; Grodzinsky, A.J.en
dc.identifier.orcidhttps://orcid.org/0000-0002-4942-3456
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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