Cargando…

RANKL synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis

INTRODUCTION: The receptor activator nuclear factor-kappaB ligand (RANKL) diffuses from articular cartilage to subchondral bone. However, the role of chondrocyte-synthesized RANKL in rheumatoid arthritis-associated juxta-articular bone loss has not yet been explored. This study aimed to determine wh...

Descripción completa

Detalles Bibliográficos
Autores principales: Martínez-Calatrava, Maria J, Prieto-Potín, Ivan, Roman-Blas, Jorge A, Tardio, Lidia, Largo, Raquel, Herrero-Beaumont, Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446534/
https://www.ncbi.nlm.nih.gov/pubmed/22709525
http://dx.doi.org/10.1186/ar3884
_version_ 1782243998831738880
author Martínez-Calatrava, Maria J
Prieto-Potín, Ivan
Roman-Blas, Jorge A
Tardio, Lidia
Largo, Raquel
Herrero-Beaumont, Gabriel
author_facet Martínez-Calatrava, Maria J
Prieto-Potín, Ivan
Roman-Blas, Jorge A
Tardio, Lidia
Largo, Raquel
Herrero-Beaumont, Gabriel
author_sort Martínez-Calatrava, Maria J
collection PubMed
description INTRODUCTION: The receptor activator nuclear factor-kappaB ligand (RANKL) diffuses from articular cartilage to subchondral bone. However, the role of chondrocyte-synthesized RANKL in rheumatoid arthritis-associated juxta-articular bone loss has not yet been explored. This study aimed to determine whether RANKL produced by chondrocytes induces osteoclastogenesis and juxta-articular bone loss associated with chronic arthritis. METHODS: Chronic antigen-induced arthritis (AIA) was induced in New Zealand (NZ) rabbits. Osteoarthritis (OA) and control groups were simultaneously studied. Dual X-ray absorptiometry of subchondral knee bone was performed before sacrifice. Histological analysis and protein expression of RANKL and osteoprotegerin (OPG) were evaluated in joint tissues. Co-cultures of human OA articular chondrocytes with peripheral blood mononuclear cells (PBMCs) from healthy donors were stimulated with macrophage-colony stimulating factor (M-CSF) and prostaglandin E(2 )(PGE(2)), then further stained with tartrate-resistant acid phosphatase. RESULTS: Subchondral bone loss was confirmed in AIA rabbits when compared with controls. The expression of RANKL, OPG and RANKL/OPG ratio in cartilage were increased in AIA compared to control animals, although this pattern was not seen in synovium. Furthermore, RANKL expression and RANKL/OPG ratio were inversely related to subchondral bone mineral density. RANKL expression was observed throughout all cartilage zones of rabbits and was specially increased in the calcified cartilage of AIA animals. Co-cultures demonstrated that PGE(2)-stimulated human chondrocytes, which produce RANKL, also induce osteoclasts differentiation from PBMCs. CONCLUSIONS: Chondrocyte-synthesized RANKL may contribute to the development of juxta-articular osteoporosis associated with chronic arthritis, by enhancing osteoclastogenesis. These results point out a new mechanism of bone loss in patients with rheumatoid arthritis.
format Online
Article
Text
id pubmed-3446534
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-34465342012-09-20 RANKL synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis Martínez-Calatrava, Maria J Prieto-Potín, Ivan Roman-Blas, Jorge A Tardio, Lidia Largo, Raquel Herrero-Beaumont, Gabriel Arthritis Res Ther Research Article INTRODUCTION: The receptor activator nuclear factor-kappaB ligand (RANKL) diffuses from articular cartilage to subchondral bone. However, the role of chondrocyte-synthesized RANKL in rheumatoid arthritis-associated juxta-articular bone loss has not yet been explored. This study aimed to determine whether RANKL produced by chondrocytes induces osteoclastogenesis and juxta-articular bone loss associated with chronic arthritis. METHODS: Chronic antigen-induced arthritis (AIA) was induced in New Zealand (NZ) rabbits. Osteoarthritis (OA) and control groups were simultaneously studied. Dual X-ray absorptiometry of subchondral knee bone was performed before sacrifice. Histological analysis and protein expression of RANKL and osteoprotegerin (OPG) were evaluated in joint tissues. Co-cultures of human OA articular chondrocytes with peripheral blood mononuclear cells (PBMCs) from healthy donors were stimulated with macrophage-colony stimulating factor (M-CSF) and prostaglandin E(2 )(PGE(2)), then further stained with tartrate-resistant acid phosphatase. RESULTS: Subchondral bone loss was confirmed in AIA rabbits when compared with controls. The expression of RANKL, OPG and RANKL/OPG ratio in cartilage were increased in AIA compared to control animals, although this pattern was not seen in synovium. Furthermore, RANKL expression and RANKL/OPG ratio were inversely related to subchondral bone mineral density. RANKL expression was observed throughout all cartilage zones of rabbits and was specially increased in the calcified cartilage of AIA animals. Co-cultures demonstrated that PGE(2)-stimulated human chondrocytes, which produce RANKL, also induce osteoclasts differentiation from PBMCs. CONCLUSIONS: Chondrocyte-synthesized RANKL may contribute to the development of juxta-articular osteoporosis associated with chronic arthritis, by enhancing osteoclastogenesis. These results point out a new mechanism of bone loss in patients with rheumatoid arthritis. BioMed Central 2012 2012-06-18 /pmc/articles/PMC3446534/ /pubmed/22709525 http://dx.doi.org/10.1186/ar3884 Text en Copyright ©2012 Martínez-Calatrava et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Martínez-Calatrava, Maria J
Prieto-Potín, Ivan
Roman-Blas, Jorge A
Tardio, Lidia
Largo, Raquel
Herrero-Beaumont, Gabriel
RANKL synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis
title RANKL synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis
title_full RANKL synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis
title_fullStr RANKL synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis
title_full_unstemmed RANKL synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis
title_short RANKL synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis
title_sort rankl synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446534/
https://www.ncbi.nlm.nih.gov/pubmed/22709525
http://dx.doi.org/10.1186/ar3884
work_keys_str_mv AT martinezcalatravamariaj ranklsynthesizedbyarticularchondrocytescontributestojuxtaarticularbonelossinchronicarthritis
AT prietopotinivan ranklsynthesizedbyarticularchondrocytescontributestojuxtaarticularbonelossinchronicarthritis
AT romanblasjorgea ranklsynthesizedbyarticularchondrocytescontributestojuxtaarticularbonelossinchronicarthritis
AT tardiolidia ranklsynthesizedbyarticularchondrocytescontributestojuxtaarticularbonelossinchronicarthritis
AT largoraquel ranklsynthesizedbyarticularchondrocytescontributestojuxtaarticularbonelossinchronicarthritis
AT herrerobeaumontgabriel ranklsynthesizedbyarticularchondrocytescontributestojuxtaarticularbonelossinchronicarthritis