Abstract

Cartilage comprises a single cell type, the chondrocyte, embedded in a highly complex extracellular matrix. Disruption to the cartilage growth plate leads to reduced bone growth and results in a clinically diverse group of conditions known as genetic skeletal diseases (GSDs). Similarly, long-term degradation of articular cartilage can lead to osteoarthritis (OA), a disease characterised by joint pain and stiffness. As professionally secreting cells, chondrocytes are particularly susceptible to endoplasmic reticulum (ER) stress and this has been identified as a core disease mechanism in a group of clinically and pathologically related GSDs. If unresolved, ER stress can lead to chondrocyte cell death. Recent interest has focused on ER stress as a druggable target for GSDs and this has led to the first clinical trial for a GSD by repurposing an antiepileptic drug. Interestingly, ER stress markers have also been associated with OA in multiple cell and animal models and there is increasing interest in it as a possible therapeutic target for treatment. In summary, chondrocyte ER stress has been identified as a core disease mechanism in GSDs and as a contributory factor in OA. Thus, chondrocyte ER stress is a unifying factor for both common and rare cartilage-related diseases and holds promise as a novel therapeutic target.

Highlights

  • Cartilage comprises a single cell type, the chondrocyte, embedded in a highly complex and macromolecule-rich extracellular matrix (ECM)

  • The unfolded protein response (UPR) is initiated by the endoplasmic reticulum (ER) lumen resident chaperone glucose-regulated protein 78/binding immunoglobulin protein (GRP78/BiP) dissociating from three transmembrane-bound receptors—protein kinase RNA-like ER kinase (PERK), inositol-requiring enzyme 1 (IRE-1) and activating transcription factor 6 (ATF6)—and binding to the exposed hydrophobic residues on the unfolded protein

  • The focus of this review is to provide an update on recent advances in chondrocyte ER stress in relation to genetic skeletal disease (GSD) and OA

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Summary

Introduction

Cartilage comprises a single cell type, the chondrocyte, embedded in a highly complex and macromolecule-rich extracellular matrix (ECM). The role of the AFT6 branch of the UPR in relation to ER stress caused by the expression of mutant type X collagen has been studied in detail using cell and mouse models[16].

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