Intermittent cyclic mechanical tension promotes endplate cartilage degeneration via canonical Wnt signaling pathway and E-cadherin/β-catenin complex cross-talk

Objective: This study aimed to investigate the role of the Wnt/beta-catenin signaling pathway and E-cadherin/beta-catenin complex in intermittent cyclic mechanical tension (ICMT)-induced endplate cartilage degeneration. Design: beta-Catenin expression was measured in disc samples obtained from patients with disc degeneration and those with cervical vertebrae fracture or dislocation. Histological staining was performed to examine the disc tissue morphology and extracellular matrix after application of ICMT in vitro and in vivo. Multiple strategies were employed to examine activation of Wnt/beta-catenin signaling after ICMT application in vivo and in vitro. Co-immunoprecipitation was performed to examine the interaction between E-cadherin and beta-catenin. Pathway-specific inhibitors and an E-cadherin expression plasmid were used to regulate Wnt/beta-catenin signaling and E-cadherin expression. Results: beta-Catenin protein expression was elevated significantly, whereas cartilaginous genes were down-regulated in endplate cartilage samples obtained from patients with disc degeneration. ICMT loading led to Wnt/beta-catenin signaling activation and the loss of the chondrogenic phenotype of endplate chondrocytes in both an in vivo rabbit model and in vitro endplate chondrocyte culture system. Inhibition of Wnt/beta-catenin signaling suppressed the decrease in ICMT-induced cartilaginous gene expression. Furthermore, E-cadherin expression was inhibited by ICMT stimulation, resulting in a decrease in the interaction between E-cadherin and beta-catenin proteins. Over-expression of E-cadherin rescued the cartilaginous gene expression by enhancing the interaction between E-cadherin and beta-catenin proteins. Conclusions: ICMT promotes endplate cartilage degeneration via activation of Wnt/beta-catenin signaling and suppression of physical proteineprotein interactions between E-cadherin and beta-catenin. (C) 2015 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.