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Article
Reduced EGFR signaling enhances cartilage destruction in a mouse osteoarthritis model
Bone Research
  • Xianrong Zhang, University of Pennsylvania
  • Ji Zhu, University of Pennsylvania
  • Fei Liu, University of Pennsylvania
  • Yumei Li, The Children's Hospital of Philadelphia
  • Abhishek Chandra, University of Pennsylvania
  • L. Scott Levin, University of Pennsylvania
  • Frank Beier, Schulich School of Medicine & Dentistry
  • Motomi Enomoto-Iwamoto, University of Pennsylvania
  • Ling Qin, University of Pennsylvania
Document Type
Article
Publication Date
8-5-2014
URL with Digital Object Identifier
10.1038/boneres.2014.15
Abstract

Osteoarthritis (OA) is a degenerative joint disease and a major cause of pain and disability in older adults. We have previously identified epidermal growth factor receptor (EGFR) signaling as an important regulator of cartilage matrix degradation during epiphyseal cartilage development. To study its function in OA progression, we performed surgical destabilization of the medial meniscus (DMM) to induce OA in two mouse models with reduced EGFR activity, one with genetic modification (Egfr Wa5/+ mice) and the other one with pharmacological inhibition (gefitinib treatment). Histological analyses and scoring at 3 months post-surgery revealed increased cartilage destruction and accelerated OA progression in both mouse models. TUNEL staining demonstrated that EGFR signaling protects chondrocytes from OA-induced apoptosis, which was further confirmed in primary chondrocyte culture. Immunohistochemistry showed increased aggrecan degradation in these mouse models, which coincides with elevated amounts of ADAMTS5 and matrix metalloproteinase 13 (MMP13), the principle proteinases responsible for aggrecan degradation, in the articular cartilage after DMM surgery. Furthermore, hypoxia-inducible factor 2α (HIF2α), a critical catabolic transcription factor stimulating MMP13 expression during OA, was also upregulated in mice with reduced EGFR signaling. Taken together, our findings demonstrate a primarily protective role of EGFR during OA progression by regulating chondrocyte survival and cartilage degradation.

Citation Information
Xianrong Zhang, Ji Zhu, Fei Liu, Yumei Li, et al.. "Reduced EGFR signaling enhances cartilage destruction in a mouse osteoarthritis model" Bone Research Vol. 2 (2014)
Available at: http://works.bepress.com/frank-beier/116/