Abstract

IntroductionPathological bone changes differ considerably between inflammatory arthritic diseases and most studies have focused on bone erosion. Collagen-induced arthritis (CIA) is a model for rheumatoid arthritis, which, in addition to bone erosion, demonstrates bone formation at the time of clinical manifestations. The objective of this study was to use this model to characterise the histological and molecular changes in bone remodelling, and relate these to the clinical disease development.MethodsA histological and gene expression profiling time-course study on bone remodelling in CIA was linked to onset of clinical symptoms. Global gene expression was studied with a gene chip array system.ResultsThe main histopathological changes in bone structure and inflammation occurred during the first two weeks following the onset of clinical symptoms in the joint. Hereafter, the inflammation declined and remodelling of formed bone dominated.Global gene expression profiling showed simultaneous upregulation of genes related to bone changes and inflammation in week 0 to 2 after onset of clinical disease. Furthermore, we observed time-dependent expression of genes involved in early and late osteoblast differentiation and function, which mirrored the histopathological bone changes. The differentially expressed genes belong to the bone morphogenetic pathway (BMP) and, in addition, include the osteoblast markers integrin-binding sialoprotein (Ibsp), bone gamma-carboxyglutamate protein (Bglap1), and secreted phosphoprotein 1 (Spp1). Pregnancy-associated protein A (Pappa) and periostin (Postn), differentially expressed in the early disease phase, are proposed to participate in bone formation, and we suggest that they play a role in early bone formation in the CIA model. Comparison to human genome-wide association studies (GWAS) revealed differential expression of several genes associated with human arthritis.ConclusionsIn the CIA model, bone formation in the joint starts shortly after onset of clinical symptoms, which results in bony fusion within one to two weeks. This makes it a candidate model for investigating the relationship between inflammation and bone formation in inflammatory arthritis.Electronic supplementary materialThe online version of this article (doi:10.1186/s13075-015-0531-7) contains supplementary material, which is available to authorized users.

Highlights

  • Pathological bone changes differ considerably between inflammatory arthritic diseases and most studies have focused on bone erosion

  • By grouping the tarsal joints according to onset and duration of symptoms, we show that the process of bone formation runs in parallel with the local inflammatory process in the joint, with a concomitant differential expression of genes involved in bone remodelling

  • Development of arthritis and histopathology of Collagen-induced arthritis (CIA) from onset to decline of clinical symptoms After immunization with chicken collagen type II (CII), mean onset of arthritis was observed on day 31 ± 8.8

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Summary

Introduction

Pathological bone changes differ considerably between inflammatory arthritic diseases and most studies have focused on bone erosion. Collagen-induced arthritis (CIA) is a model for rheumatoid arthritis, which, in addition to bone erosion, demonstrates bone formation at the time of clinical manifestations. The objective of this study was to use this model to characterise the histological and molecular changes in bone remodelling, and relate these to the clinical disease development. The balance between anabolic and catabolic bone remodelling, differs between the inflammatory arthritic diseases rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS). Collagen-induced arthritis (CIA) is a model for RA both due to its construct validity, including autoimmune reaction to collagen type II and MHC class II dependency, and due to its face validity, that is severe bone destruction. Disease development ends in bony fusion (ankylosis) of the destroyed joints, which could

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