Dynamic compression inhibits cytokine-mediated type II collagen degradation.

Articular cartilage Asteoarthritis Bovine explants Dynamic mechanical compression Translational research Type II collagen

Journal

Osteoarthritis and cartilage open
ISSN: 2665-9131
Titre abrégé: Osteoarthr Cartil Open
Pays: England
ID NLM: 101767068

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 19 08 2021
accepted: 22 06 2022
entrez: 7 12 2022
pubmed: 8 12 2022
medline: 8 12 2022
Statut: epublish

Résumé

To examine the effect of dynamic compressive loading applied intermittently on bovine cartilage explants stimulated with proinflammatory cytokines over 21 days. Cartilage explants were cultured for 21 days with Oncostatin M and TNFα (O ​+ ​T) [10/5 ​ng/mL] or in culture medium alone (w/o). The explants were either left free-swelling or subjected to dynamic compressive loading of 20 ​min, at 1 ​Hz, with loads ranging between 0.1 and 1 ​MPa, 5 times weekly. Metabolic activity was measured once weekly using Alamar Blue and cartilage turnover was assessed with biomarkers targeting degradation fragments of aggrecan (AGNx1) and type II collagen (C2M). Glycosaminoglycan degradation was quantified was the DMMB assay. Furthermore, explant weight and histological analysis was used to assess the cartilage degradation. Dynamic compression of cartilage explants attenuated the O ​+ ​T-mediated C2M release on day 21 with 40% (p ​= ​0.0068) compared to the unloaded explants. Additionally, the change in explant weight from day -1 to day 21 showed that O ​+ ​T stimulation alone mediated a cartilage loss of 11%, whereas O ​+ ​T-stimulated explants subjected to compressive loading demonstrated a decreased cartilage weight loss of 6%, which was supported by the histological analysis. However, loading had no effect on aggrecan degradation. In cartilage explants cultured in a proinflammatory milieu, dynamic compressive loading confers anti-catabolic effects, inhibiting type II collagen degradation and reducing explant cartilage loss. These results demonstrate that compressive loading alters cartilage tissue turnover and enforces the need to include mechanical loading in a translation

Identifiants

pubmed: 36474783
doi: 10.1016/j.ocarto.2022.100292
pii: S2665-9131(22)00060-7
pmc: PMC9718275
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100292

Informations de copyright

© 2022 Published by Elsevier Ltd on behalf of Osteoarthritis Research Society International (OARSI).

Déclaration de conflit d'intérêts

CST, ACBJ, and MAK are full-time employees at Nordic Bioscience A/S. CST, ACBJ and MAK hold stocks in Nordic Bioscience. AEN and FRG have no conflicts to declare.

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Auteurs

Amalie Engstrøm (A)

Immunoscience, Nordic Bioscience, Herlev, Denmark.
Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Frederik S Gillesberg (FS)

Immunoscience, Nordic Bioscience, Herlev, Denmark.
University of Copenhagen, Copenhagen, Denmark.

Anne-Christine Bay Jensen (AC)

Immunoscience, Nordic Bioscience, Herlev, Denmark.

Morten A Karsdal (MA)

Immunoscience, Nordic Bioscience, Herlev, Denmark.

Christian S Thudium (CS)

Immunoscience, Nordic Bioscience, Herlev, Denmark.

Classifications MeSH