Conditional activation of β-catenin signaling in mice leads to severe defects in intervertebral disc tissue

Meina Wang, Dezhi Tang, Bing Shu, Baoli Wang, Hongting Jin, Suyang Hao, Karen A. Dresser, Jie Shen, Hee Jeong Im, Erik R. Sampson, Paul T. Rubery, Michael J. Zuscik, Edward M. Schwarz, Regis J. O'Keefe, Yongjun Wang, Di Chen

Research output: Contribution to journalArticle

72 Scopus citations

Abstract

Objective The incidence of low back pain is extremely high and is often linked to intervertebral disc (IVD) degeneration. The mechanism of this disease is currently unknown. This study was undertaken to investigate the role of β-catenin signaling in IVD tissue function. Methods β-catenin protein levels were measured by immunohistochemical analysis of disc samples obtained from patients with disc degeneration and from normal subjects. To generate β-catenin conditional activation (cAct) mice, Col2a1-CreER T2-transgenic mice were bred with β-catenin fx(Ex3)/fx(Ex3) mice. Changes in disc tissue morphology and function were examined by micro-computed tomography, histologic analysis, and real-time polymerase chain reaction assays. Results β-catenin protein was up-regulated in disc tissue samples from patients with disc degeneration. To assess the effects of increased β-catenin levels on disc tissue, we generated β-catenin cAct mice. Overexpression of β-catenin in disc cells led to extensive osteophyte formation in 3- and 6-month-old β-catenin cAct mice, which were associated with significant changes in the cells and extracellular matrix of disc tissue and growth plate. Gene expression analysis demonstrated that activation of β-catenin enhanced runt-related transcription factor 2-dependent Mmp13 and Adamts5 expression. Moreover, genetic ablation of Mmp13 or Adamts5 on the β-catenin cAct background, or treatment of β-catenin cAct mice with a specific matrix metalloproteinase 13 inhibitor, ameliorated the mutant phenotype. Conclusion Our findings indicate that the β-catenin signaling pathway plays a critical role in disc tissue function.

Original languageEnglish (US)
Pages (from-to)2611-2623
Number of pages13
JournalArthritis and Rheumatism
Volume64
Issue number8
DOIs
StatePublished - Aug 2012

ASJC Scopus subject areas

  • Immunology and Allergy
  • Rheumatology
  • Immunology
  • Pharmacology (medical)

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