BMC Research Notes (Mar 2011)

A microarray analysis of full depth knee cartilage of ovariectomized rats

  • Letzkus Martin,
  • Steadtler Frank,
  • Azria Moïse,
  • Segovia-Silvestre Toni,
  • Nielsen Rasmus H,
  • Bay-Jensen Anne C,
  • Hartmann Nicole,
  • Brachat Arndt H,
  • Karsdal Morten A

DOI
https://doi.org/10.1186/1756-0500-4-63
Journal volume & issue
Vol. 4, no. 1
p. 63

Abstract

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Abstract Background This short communication focuses the on articular cartilage and the subchondral bone, both of which play important roles in the development of osteoarthritis (OA). There are indications that estrogen-deficiency, as the post-menopausal state, accelerate the development of OA. Findings We investigated, which extracellular matrix (ECM) protein, proteases and different pro-inflammatory factors was up- or down-regulated in the knee joint tissue in response to estrogen-deficiency in rats induced by ovariectomy. These data support previous findings that several metalloproteinases (MMPs) and cysteine proteases are co-regulated with numerous collagens and proteoglycans that are important for cartilage integrity. Furthermore quite a few pro-inflammatory cytokines were regulated by estrogen deprivation. Conclusion We found multiple genes where regulated in the joint by estrogen-deficiency, many of which correspond well with our current knowledge of the pathogenesis of OA. It supports that estrogen-deficiency (e.g. OVX) may accelerate joint deterioration. However, there are also data that draw attention the need for better understanding of the synergy between proteases and tissue turnover.