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A single blunt impact on cartilage promotes fibronectin fragmentation and upregulates cartilage degrading stromelysin‐1/matrix metalloproteinase‐3 in a bovine ex vivo model
Author(s) -
Ding Lei,
Guo Danping,
Homandberg Gene A.,
Buckwalter Joseph A.,
Martin James A.
Publication year - 2014
Publication title -
journal of orthopaedic research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.22610
Subject(s) - cartilage , matrix metalloproteinase , aggrecanase , fibronectin , aggrecan , explant culture , microbiology and biotechnology , cartilage oligomeric matrix protein , chemistry , osteoarthritis , metalloproteinase , matrix metalloproteinase 3 , matrix (chemical analysis) , immunology , pathology , anatomy , extracellular matrix , medicine , in vitro , biology , biochemistry , articular cartilage , alternative medicine , chromatography
ABSTRACT Post‐traumatic osteoarthritis (PTOA) is characterized by progressive cartilage degeneration in injured joints. Since fibronectin‐fragments (Fn‐fs) degrade cartilage mainly through up‐regulating matrix metalloproteinases (MMPs) and pro‐inflammatory cytokines, we hypothesized that Fn‐fs play a key role in PTOA by promoting chondrolysis in and around injured cartilage. To test this hypothesis, we profiled the catabolic events focusing on fibronectin fragmentation and proteinase expression in bovine osteochondral explants following a single blunt impact on cartilage with a drop tower device which created partial‐thickness tissue damage. Injured and control explants were cultured for up to 14 days. The presence of Fn‐fs, MMPs (‐1, ‐3, ‐13), ADAMTS‐5 in culture media and in cartilage was determined with immunoblotting. The daily proteoglycan (PG) depletion of cartilage matrix was assessed with DMMB assay. The effect of explant‐conditioned media on chondrocytes was also examined with immunoblotting. Impacted cartilage released significantly higher amount of native Fn, three chondrolytic Fn‐fs and PG than non‐impacted controls did. Those increases coincided with up‐regulation of MMP‐3 both in culture media and in impacted cartilage. These findings support our hypothesis that PTOA may be propelled by Fn‐fs which act as catabolic mediators through up‐regulating cartilage‐damaging proteinases. © 2014 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 32:811–818, 2014.