Document Detail


Rac1 is required for matrix metalloproteinase 13 production by chondrocytes in response to fibronectin fragments.
MedLine Citation:
PMID:  23460186     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: Matrix fragments, including fibronectin (FN) fragments, accumulate during the development of osteoarthritis (OA), stimulating the production of chondrocyte matrix metalloproteinase (MMP). The objective of this study was to determine the role of the small GTPase Rac1 in chondrocyte signaling stimulated by FN fragments, which results in MMP-13 production.
METHODS: Normal human cartilage was obtained from tissue donors and OA cartilage from knee arthroplasty specimens. Rac1 activity was modulated with a chemical inhibitor, by knockdown with small interfering RNA (siRNA), or with constitutively active Rac or dominant-negative Rac adenovirus. Cells were treated with FN fragments, with or without epidermal growth factor (EGF) or transforming growth factor α (TGFα), which are known activators of Rac. Rac1 activity was measured with a colorimetric activity enzyme-linked immunosorbent assay, a pulldown assay, and immunostaining with a monoclonal antibody against active Rac.
RESULTS: Chemical inhibition of Rac1, as well as knockdown by siRNA and expression of dominant-negative Rac, blocked FN fragment-stimulated MMP-13 production, while expression of constitutively active Rac increased MMP-13 production. Inhibition of Rho-associated kinase had no effect. EGF and TGFα, but not FN fragments, increased Rac1 activity and promoted the increase in MMP-13 above that achieved by stimulation with FN fragments alone. Active Rac was detected in OA cartilage by immunostaining.
CONCLUSION: Rac1 is required for FN fragment-induced signaling that results in increased MMP-13 production. EGF receptor ligands, which activate Rac, can promote this effect. The presence of active Rac in OA cartilage and the ability of Rac to stimulate MMP-13 production suggest that it could play a role in the cartilage matrix destruction seen in OA.
Authors:
David L Long; Jeffrey S Willey; Richard F Loeser
Related Documents :
12675136 - Effects of sex hormones, forskolin, and nicotine on choline acetyltransferase activity ...
11443226 - Polyamines: new cues in cellular signal transduction.
10221996 - Microplate enzyme-coupled assays of mevalonate and phosphomevalonate kinase from cathar...
2992596 - Complete co-purification of choline kinase and ethanolamine kinase from rat kidney and ...
18266916 - A nima-related protein kinase suppresses ectopic outgrowth of epidermal cells through i...
8797806 - Intramolecular interactions regulate serine/threonine phosphorylation of vinculin.
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Arthritis and rheumatism     Volume:  65     ISSN:  1529-0131     ISO Abbreviation:  Arthritis Rheum.     Publication Date:  2013 Jun 
Date Detail:
Created Date:  2013-06-03     Completed Date:  2013-08-13     Revised Date:  2014-06-03    
Medline Journal Info:
Nlm Unique ID:  0370605     Medline TA:  Arthritis Rheum     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1561-8     Citation Subset:  AIM; IM    
Copyright Information:
Copyright © 2013 by the American College of Rheumatology.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Cartilage, Articular / enzymology*
Cells, Cultured
Chondrocytes / enzymology*
Fibronectins / metabolism*
Humans
Immunoblotting
Immunohistochemistry
Matrix Metalloproteinase 13 / metabolism*
Osteoarthritis / metabolism*
Real-Time Polymerase Chain Reaction
Signal Transduction
rac1 GTP-Binding Protein / metabolism*
Grant Support
ID/Acronym/Agency:
R37 AR049003/AR/NIAMS NIH HHS; R37-AR-49003-11/AR/NIAMS NIH HHS
Chemical
Reg. No./Substance:
0/Fibronectins; 0/RAC1 protein, human; EC 3.4.24.-/MMP13 protein, human; EC 3.4.24.-/Matrix Metalloproteinase 13; EC 3.6.5.2/rac1 GTP-Binding Protein
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  mTOR signaling for biological control and cancer.
Next Document:  Pharmacological potentials of Syzygium cumini: A review.