Deletion of 12/15-lipoxygenase accelerates the development of aging-associated and instability-induced osteoarthritis

Osteoarthritis Cartilage. 2017 Oct;25(10):1719-1728. doi: 10.1016/j.joca.2017.07.001. Epub 2017 Jul 8.

Abstract

Objective: 12/15-Lipoxygenase (12/15-LOX) catalyzes the generation of various anti-inflammatory lipid mediators, and has been implicated in several inflammatory and degenerative diseases. However, there is currently no evidence that 12/15-LOX has a role in osteoarthritis (OA). The aim of this study was to investigate the role of 12/15-LOX in the pathogenesis of OA.

Methods: The development of aging-associated and destabilization of the medial meniscus (DMM)-induced OA were compared in 12/15-LOX-deficient (12/15-LOX-/-) and wild-type (WT) mice. The extent of cartilage damage was evaluated by histology. The expression of OA markers was evaluated by immunohistochemistry and RT-PCR. Cartilage explants were stimulated with IL-1α in the absence or presence of the 12/15-LOX metabolites, 15-hydroxyeicosatetraenoic acids (15-HETE), 13-hydroxyoctadecadienoic acid (13-HODE) or lipoxin A4 (LXA4), and the levels of matrix metalloproteinases-13 (MMP-13), Nitric oxide (NO) and prostaglandin E2 (PGE2) were determined. The effect of LXA4 on the progression of OA was evaluated in wild type (WT) mice.

Results: The expression of 12/15-LOX in cartilage increased during the progression of DMM-induced OA and with aging in WT mice. Cartilage degeneration was more severe in 12/15-LOX-/- mice compared to WT mice in both models of OA, and this was associated with increased expression of MMP-13, a disintegrin and metalloproteinase with thrombospondin motifs, aggrecanases (ADAMTS5), inducible NO synthases (iNOS), and mPGES-1. Treatment of cartilage explants with 12/15-LOX metabolites, suppressed IL-1α-induced production of MMP-13, NO and PGE2, with LXA4 being the most potent. Intra-peritoneal injection of LXA4 reduced the severity of DMM-induced cartilage degradation.

Conclusions: These data suggest an important role of 12/15-LOX in the pathogenesis of OA. They also suggest that activation of this pathway may provide a novel strategy for prevention and treatment of OA.

Keywords: 12/15-LOX; Cartilage; LXA4; Osteoarthritis.

MeSH terms

  • Aging / metabolism
  • Aging / pathology
  • Animals
  • Arachidonate 12-Lipoxygenase / deficiency
  • Arachidonate 12-Lipoxygenase / genetics
  • Arachidonate 12-Lipoxygenase / physiology*
  • Arachidonate 15-Lipoxygenase / deficiency
  • Arachidonate 15-Lipoxygenase / genetics
  • Arachidonate 15-Lipoxygenase / physiology*
  • Arthritis, Experimental / enzymology*
  • Arthritis, Experimental / etiology
  • Arthritis, Experimental / prevention & control
  • Cartilage, Articular / metabolism
  • Disease Progression
  • Inflammation Mediators / metabolism
  • Joint Instability / complications
  • Lipoxins / therapeutic use
  • Male
  • Mice, Knockout
  • Osteoarthritis / enzymology*
  • Osteoarthritis / etiology
  • Osteoarthritis / prevention & control
  • Tibial Meniscus Injuries / complications
  • Tissue Culture Techniques
  • Up-Regulation

Substances

  • 12-15-lipoxygenase
  • Inflammation Mediators
  • Lipoxins
  • lipoxin A4
  • Arachidonate 12-Lipoxygenase
  • Arachidonate 15-Lipoxygenase