Early Response of Mouse Joint Tissue to Noninvasive Knee Injury Suggests Treatment Targets. Issue 5 (May 2014)
- Record Type:
- Journal Article
- Title:
- Early Response of Mouse Joint Tissue to Noninvasive Knee Injury Suggests Treatment Targets. Issue 5 (May 2014)
- Main Title:
- Early Response of Mouse Joint Tissue to Noninvasive Knee Injury Suggests Treatment Targets
- Authors:
- Wu, P.
Holguin, N.
Silva, M. J.
Fu, M.
Liao, W.
Sandell, L. J. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="art38375-sec-0001" sec-type="section"> <title>Objective</title> <p>Joint trauma can lead to a spectrum of acute lesions, including cartilage degradation, ligament or meniscus tears, and synovitis, all potentially associated with osteoarthritis (OA). This study was undertaken to generate and validate a murine model of knee joint trauma following noninvasive controlled injurious compression in vivo.</p> </sec> <sec id="art38375-sec-0002" sec-type="section"> <title>Methods</title> <p>The right knees of 8‐week‐old mice were placed in a hyperflexed position and subjected to compressive joint loading at 1 of 3 peak forces (3N, 6N, or 9N) for 60 cycles in a single loading period and harvested on days 5, 9, and 14 after loading (n = 3–5 for each time point and for each loading). The left knees were not loaded and were used as the contralateral control. Histologic, immunohistochemical, and enzyme‐linked immunosorbent assay analyses were performed to evaluate acute pathologic features in chondrocyte viability, cartilage matrix metabolism, synovial reaction, and serum cartilage oligomeric matrix protein (COMP) levels.</p> </sec> <sec id="art38375-sec-0003" sec-type="section"> <title>Results</title> <p>Acute joint pathology was associated with increased injurious loads. All loading regimens induced chondrocyte apoptosis, cartilage matrix degradation, disruption of cartilage collagen fibril<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="art38375-sec-0001" sec-type="section"> <title>Objective</title> <p>Joint trauma can lead to a spectrum of acute lesions, including cartilage degradation, ligament or meniscus tears, and synovitis, all potentially associated with osteoarthritis (OA). This study was undertaken to generate and validate a murine model of knee joint trauma following noninvasive controlled injurious compression in vivo.</p> </sec> <sec id="art38375-sec-0002" sec-type="section"> <title>Methods</title> <p>The right knees of 8‐week‐old mice were placed in a hyperflexed position and subjected to compressive joint loading at 1 of 3 peak forces (3N, 6N, or 9N) for 60 cycles in a single loading period and harvested on days 5, 9, and 14 after loading (n = 3–5 for each time point and for each loading). The left knees were not loaded and were used as the contralateral control. Histologic, immunohistochemical, and enzyme‐linked immunosorbent assay analyses were performed to evaluate acute pathologic features in chondrocyte viability, cartilage matrix metabolism, synovial reaction, and serum cartilage oligomeric matrix protein (COMP) levels.</p> </sec> <sec id="art38375-sec-0003" sec-type="section"> <title>Results</title> <p>Acute joint pathology was associated with increased injurious loads. All loading regimens induced chondrocyte apoptosis, cartilage matrix degradation, disruption of cartilage collagen fibril arrangement, and increased levels of serum COMP. We also observed that 6N loading induced mild synovitis by day 5, whereas at 9N, with tearing of the anterior cruciate ligament, severe posttraumatic synovitis and ectopic cartilage formation were observed.</p> </sec> <sec id="art38375-sec-0004" sec-type="section"> <title>Conclusion</title> <p>We have established a murine model of knee joint trauma with different degrees of overloading in vivo. Our results suggest that immediate therapies particularly targeted to apoptosis and synovial cell proliferation could affect the acute posttraumatic reaction to potentially limit chronic consequences and OA.</p> </sec> </abstract> … (more)
- Is Part Of:
- Arthritis & rheumatology. Volume 66:Issue 5(2014)
- Journal:
- Arthritis & rheumatology
- Issue:
- Volume 66:Issue 5(2014)
- Issue Display:
- Volume 66, Issue 5 (2014)
- Year:
- 2014
- Volume:
- 66
- Issue:
- 5
- Issue Sort Value:
- 2014-0066-0005-0000
- Page Start:
- 1256
- Page End:
- 1265
- Publication Date:
- 2014-05
- Subjects:
- Arthritis -- Periodicals
Rheumatism -- Periodicals
616.72 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2326-5205 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/art.38375 ↗
- Languages:
- English
- ISSNs:
- 2326-5191
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1733.820000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3879.xml