Environmental disruption of circadian rhythm predisposes mice to osteoarthritis-like changes in knee joint

J Cell Physiol. 2015 Sep;230(9):2174-2183. doi: 10.1002/jcp.24946.


Circadian rhythm dysfunction is linked to many diseases, yet pathophysiological roles in articular cartilage homeostasis and degenerative joint disease including osteoarthritis (OA) remains to be investigated in vivo. Here, we tested whether environmental or genetic disruption of circadian homeostasis predisposes to OA-like pathological changes. Male mice were examined for circadian locomotor activity upon changes in the light:dark (LD) cycle or genetic disruption of circadian rhythms. Wild-type (WT) mice were maintained on a constant 12 h:12 h LD cycle (12:12 LD) or exposed to weekly 12 h phase shifts. Alternatively, male circadian mutant mice (Clock(Δ19) or Csnk1e(tau) mutants) were compared with age-matched WT littermates that were maintained on a constant 12:12 LD cycle. Disruption of circadian rhythms promoted osteoarthritic changes by suppressing proteoglycan accumulation, upregulating matrix-degrading enzymes and downregulating anabolic mediators in the mouse knee joint. Mechanistically, these effects involved activation of the PKCδ-ERK-RUNX2/NFκB and β-catenin signaling pathways, stimulation of MMP-13 and ADAMTS-5, as well as suppression of the anabolic mediators SOX9 and TIMP-3 in articular chondrocytes of phase-shifted mice. Genetic disruption of circadian homeostasis does not predispose to OA-like pathological changes in joints. Our results, for the first time, provide compelling in vivo evidence that environmental disruption of circadian rhythms is a risk factor for the development of OA-like pathological changes in the mouse knee joint.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CLOCK Proteins / genetics*
  • Cartilage, Articular / metabolism*
  • Cartilage, Articular / pathology
  • Circadian Rhythm / genetics*
  • Circadian Rhythm / physiology
  • Core Binding Factor Alpha 1 Subunit / biosynthesis
  • Disease Susceptibility
  • Environment
  • Homeostasis / genetics
  • Humans
  • Knee Joint / metabolism
  • Knee Joint / physiopathology
  • MAP Kinase Signaling System / genetics
  • Matrix Metalloproteinase 13 / biosynthesis
  • Mice
  • Motor Activity / genetics
  • Motor Activity / physiology
  • Osteoarthritis, Knee / genetics*
  • Osteoarthritis, Knee / physiopathology


  • Core Binding Factor Alpha 1 Subunit
  • Runx2 protein, mouse
  • CLOCK Proteins
  • Clock protein, mouse
  • Matrix Metalloproteinase 13