Hyaluronic acid suppresses the expression of metalloproteinases in osteoarthritic cartilage stimulated simultaneously by interleukin 1β and mechanical load

Florian Pohlig, Florian Guell, Ulrich Lenze, Florian W. Lenze, Heinrich M.L. Mühlhofer, Johannes Schauwecker, Andreas Toepfer, Philipp Mayer-Kuckuk, Rüdiger Von Eisenhart-Rothe, Rainer Burgkart, Gian M. Salzmann

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

17 Zitate (Scopus)

Abstract

Purpose In patients with osteoarthritis (OA), intraarticular injection of hyaluronic acid (HA) frequently results in reduced pain and improved function for prolonged periods of time, i.e. more than 6 months. However, the mechanisms underlying these effects are not fully understood. Our underlying hypothesis is that HA modifies the enzymatic breakdown of joint tissues. Methods To test this hypothesis, we examined osteochondral cylinders from 12 OA patients. In a bioreactor, these samples were stimulated by interleukin 1β (Il1ß) (2 ng/ml) plus mechanical load (2.0 Mpa at 0.5 Hz horizontal and 0.1 Hz vertical rotation), thus the experimental setup recapitulated both catabolic and anabolic clues of the OA joint. Results Upon addition of HA at either 1 or 3 mg/ml, we observed a significant suppression of expression of metalloproteinase (MMP)-13. A more detailed analysis based on the Kellgren and Lawrence (K&L) OA grade, showed a much greater degree of suppression ofMMP-13 expression in grade IV as compared to grade II OA. In contrast to the observedMMP-13 suppression, treatment with HA resulted in a suppression ofMMP-1 expression only at 1 mg/ml HA, while MMP-2 expression was not significantly affected by either HA concentration. Conclusion Together, these data suggest that under concurrent catabolic and anabolic stimulation, HA exhibits a pronounced suppressive effect on MMP-13. In the long-run these findings maybenefit the development of treatment strategies aimed at blocking tissue degradation in OA patients.

OriginalspracheEnglisch
Aufsatznummere0150020
FachzeitschriftPLoS ONE
Jahrgang11
Ausgabenummer3
DOIs
PublikationsstatusVeröffentlicht - März 2016
Extern publiziertJa

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