dc.contributor.author | Grodzinsky, Alan J. | |
dc.contributor.author | Wheeler, Cameron A. | |
dc.contributor.author | Jafarzadeh, Seyed R. | |
dc.contributor.author | Rocke, David M. | |
dc.date.accessioned | 2011-10-26T17:58:35Z | |
dc.date.available | 2011-10-26T17:58:35Z | |
dc.date.issued | 2009-02 | |
dc.date.submitted | 2009-02 | |
dc.identifier.issn | 1063-4584 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/66590 | |
dc.description.abstract | Objective
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.sponsorship | National Institutes of Health (U.S.) (grant R01-AR33236) | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (grant R01-HG003352) | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (grant P42-ES04699) | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (grant T32-EB006348) | en_US |
dc.language.iso | en_US | |
dc.publisher | Elsevier Ltd. | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1016/j.joca.2009.02.001 | en_US |
dc.rights | Creative Commons Attribution-Noncommercial-Share Alike 3.0 | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/3.0/ | en_US |
dc.source | PubMed Central | en_US |
dc.title | IGF-1 does not moderate the time-dependent transcriptional patterns of key homeostatic genes induced by sustained compression of bovine cartilage | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Wheeler, 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.department | Massachusetts Institute of Technology. Department of Biological Engineering | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Mechanical Engineering | en_US |
dc.contributor.approver | Grodzinsky, Alan J. | |
dc.contributor.mitauthor | Grodzinsky, Alan J. | |
dc.contributor.mitauthor | Wheeler, Cameron A. | |
dc.relation.journal | Osteoarthritis and Cartilage | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Wheeler, C.A.; Jafarzadeh, S.R.; Rocke, D.M.; Grodzinsky, A.J. | en |
dc.identifier.orcid | https://orcid.org/0000-0002-4942-3456 | |
mit.license | OPEN_ACCESS_POLICY | en_US |
mit.metadata.status | Complete | |