The collagenase-induced osteoarthritis (CIOA) model: Where mechanical damage meets inflammation
Weber, Patrick; Bevc, Kajetana; Fercher, David; Kauppinen, Sami; Zhang, Shipin; Asadikorayem, Maryam; Marin, Lucia Baixauli; Zhang, Tanqi; Frondelius, Tuomas; Salzmann, Gian; Bruhin, Valentino; Hax, Jakob; Barreto, Gonçalo; Finnilä, Mikko A.J.; Zenobi-Wong, Marcy (2024-10-24)
Weber, Patrick
Bevc, Kajetana
Fercher, David
Kauppinen, Sami
Zhang, Shipin
Asadikorayem, Maryam
Marin, Lucia Baixauli
Zhang, Tanqi
Frondelius, Tuomas
Salzmann, Gian
Bruhin, Valentino
Hax, Jakob
Barreto, Gonçalo
Finnilä, Mikko A.J.
Zenobi-Wong, Marcy
Elsevier
24.10.2024
Patrick Weber, Kajetana Bevc, David Fercher, Sami Kauppinen, Shipin Zhang, Maryam Asadikorayem, Lucia Baixauli Marin, Tanqi Zhang, Tuomas Frondelius, Gian Salzmann, Valentino Bruhin, Jakob Hax, Gonçalo Barreto, Mikko A.J. Finnilä, Marcy Zenobi-Wong, The collagenase-induced osteoarthritis (CIOA) model: Where mechanical damage meets inflammation, Osteoarthritis and Cartilage Open, Volume 6, Issue 4, 2024, 100539, ISSN 2665-9131, https://doi.org/10.1016/j.ocarto.2024.100539
https://creativecommons.org/licenses/by/4.0/
© 2024 The Author(s). Published by Elsevier Ltd on behalf of Osteoarthritis Research Society International (OARSI). This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
© 2024 The Author(s). Published by Elsevier Ltd on behalf of Osteoarthritis Research Society International (OARSI). This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:oulu-202411156757
https://urn.fi/URN:NBN:fi:oulu-202411156757
Tiivistelmä
Abstract
Objective:
To characterize inflammatory and mechanical changes in the collagenase-induced OA (CIOA) model in rats.
Design:
Skeletally mature, 6-month-old Wistar rats received unilateral intraarticular injections of saline, 500 U or 1000 U of collagenase on days 0 and 2 of the study. Joint tissues were harvested on either day 4 or 70 to evaluate the acute and long-term changes. Blood biomarkers, gait asymmetry and mechanical hyperalgesia were assessed repeatedly up until day 70.
Results:
The intraarticular injection of collagenase triggered an increase in cartilage degeneration and bone resorption over time, particularly for 1000 U. Similarly, mild synovitis was observed on day 70 with an increased number of synovial lining cells, increased fibrosis, and infiltration of peripheral macrophages. Mechanistically, these findings were linked to a dose-related mechanical weakening of the anterior cruciate ligament (ACL), which caused persistent joint destabilization throughout the study. Furthermore, the collagenase injection triggered acute inflammation and swelling of the synovium on day 4 and an acute systemic inflammatory response with increased cytokine and peripheral blood immune cell levels. While mild synovitis persisted until day 70, the systemic inflammatory response returned to control levels after 8 days. Similarly, the observed acute changes in gait and mechanical hyperalgesia also returned to baseline after 21 days.
Conclusion:
By evaluating inflammatory and mechanical factors at different doses and timepoints, our characterization enables a more targeted study design and increases the clinical relevance of future studies involving the CIOA model.
Objective:
To characterize inflammatory and mechanical changes in the collagenase-induced OA (CIOA) model in rats.
Design:
Skeletally mature, 6-month-old Wistar rats received unilateral intraarticular injections of saline, 500 U or 1000 U of collagenase on days 0 and 2 of the study. Joint tissues were harvested on either day 4 or 70 to evaluate the acute and long-term changes. Blood biomarkers, gait asymmetry and mechanical hyperalgesia were assessed repeatedly up until day 70.
Results:
The intraarticular injection of collagenase triggered an increase in cartilage degeneration and bone resorption over time, particularly for 1000 U. Similarly, mild synovitis was observed on day 70 with an increased number of synovial lining cells, increased fibrosis, and infiltration of peripheral macrophages. Mechanistically, these findings were linked to a dose-related mechanical weakening of the anterior cruciate ligament (ACL), which caused persistent joint destabilization throughout the study. Furthermore, the collagenase injection triggered acute inflammation and swelling of the synovium on day 4 and an acute systemic inflammatory response with increased cytokine and peripheral blood immune cell levels. While mild synovitis persisted until day 70, the systemic inflammatory response returned to control levels after 8 days. Similarly, the observed acute changes in gait and mechanical hyperalgesia also returned to baseline after 21 days.
Conclusion:
By evaluating inflammatory and mechanical factors at different doses and timepoints, our characterization enables a more targeted study design and increases the clinical relevance of future studies involving the CIOA model.
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