RANKL protein is expressed at the pannus-bone interface at sites of articular bone erosion in rheumatoid arthritis

Pettit, A. R., Walsh, N. C., Manning, C., Goldring, S. R. and Gravallese, E. M. (2006) RANKL protein is expressed at the pannus-bone interface at sites of articular bone erosion in rheumatoid arthritis. Rheumatology, 45 9: 1068-1076. doi:10.1093/rheumatology/kel045


Author Pettit, A. R.
Walsh, N. C.
Manning, C.
Goldring, S. R.
Gravallese, E. M.
Title RANKL protein is expressed at the pannus-bone interface at sites of articular bone erosion in rheumatoid arthritis
Journal name Rheumatology   Check publisher's open access policy
ISSN 1462-0324
Publication date 2006
Sub-type Article (original research)
DOI 10.1093/rheumatology/kel045
Volume 45
Issue 9
Start page 1068
End page 1076
Total pages 9
Place of publication Oxford
Publisher Oxford University Press
Collection year 2006
Language eng
Subject C1
321028 Rheumatology and Arthritis
321017 Orthopaedics
730114 Skeletal system and disorders (incl. arthritis)
Abstract Objectives. Receptor activator of NF-kappa B ligand (RANKL) and osteoprotegerin (OPG) have been demonstrated to be critical regulators of osteoclast generation and activity. In addition, RANKL has been implicated as an important mediator of bone erosion in rheumatoid arthritis (RA). However, the expression of RANKL and OPG at sites of pannus invasion into bone has not been examined. The present study was undertaken to further elucidate the contribution of this cytokine system to osteoclastogenesis and subsequent bone erosion in RA by examining the pattern of protein expression for RANKL, OPG and the receptor activator of NF-kappa B (RANK) in RA at sites of articular bone erosion. Methods. Tissues from 20 surgical procedures from 17 patients with RA were collected as discarded materials. Six samples contained only synovium or tenosynovium remote from bone, four samples contained pannus-bone interface with adjacent synovium and 10 samples contained both synovium remote from bone and pannu-bone interface with adjacent synovium. Immunohistochemistry was used to characterize the cellular pattern of RANKL, RANK and OPG protein expression immediately adjacent to and remote from sites of bone erosion. Results. Cellular expression of RANKL protein was relatively restricted in the bone microenvironment; staining was focal and confined largely to sites of osteoclast-mediated erosion at the pannus-bone interface and at sites of subchondral bone erosion. RANK-expressing osteoclast precursor cells were also present in these sites. OPG protein expression was observed in numerous cells in synovium remote from bone but was more limited at sites of bone erosion, especially in regions associated with RANKL expression. Conclusions. The pattern of RANKL and OPG expression and the presence of RANK-expressing osteoclast precursor cells at sites of bone erosion in RA contributes to the generation of a local microenvironment that favours osteoclast differentiation and activity. These data provide further evidence implicating RANKL in the pathogenesis of arthritis-induced joint destruction.
Keyword Rheumatoid Arthritis
Osteoclasts
Rankl
Opg
Rank
Bone Erosion
Rheumatology
Kappa-b Ligand
Tumor-necrosis-factor
Collagen-induced Arthritis
Osteoclast Differentiation Factor
Mediated Joint Destruction
Inhibitory Factor Ocif
In-vitro Model
Receptor Activator
Factor-alpha
Osteoprotegerin Ligand
Q-Index Code C1

Document type: Journal Article
Sub-type: Article (original research)
Collections: 2007 Higher Education Research Data Collection
Institute for Molecular Bioscience - Publications
 
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Created: Wed, 15 Aug 2007, 09:09:07 EST