Interleukin 34 expression is associated with synovitis severity in rheumatoid arthritis patients

被引：151

作者：

Chemel, M. ^{[1
,2
,3
]}

Le Goff, B. ^{[1
,2
,3
]}

Brion, R. ^{[1
,2
,3
]}

Cozic, C. ^{[1
,2
,3
]}

Berreur, M. ^{[1
,2
]}

Amiaud, J. ^{[1
,2
]}

Bougras, G. ^{[1
,2
]}

Touchais, S. ^{[3
]}

Blanchard, F. ^{[1
,2
]}

Heymann, M. F. ^{[1
,2
]}

Berthelot, J. M. ^{[1
,2
,3
]}

Verrecchia, F. ^{[1
,2
]}

Heymann, D. ^{[1
,2
,3
]}

机构：

[1] INSERM, UMR S 957, Fac Med, F-44035 Nantes 1, France

[2] Univ Nantes, Nantes Atlantique Univ, Lab Physiopathol Resorpt Osseuse & Therapie Tumeu, Nantes, France

[3] CHU Nantes, F-44035 Nantes 01, France

来源：

ANNALS OF THE RHEUMATIC DISEASES | 2012年 / 71卷 / 01期

关键词：

COLONY-STIMULATING FACTOR; PRO-INFLAMMATORY CYTOKINES; NF-KAPPA-B; GENE-EXPRESSION; KEY ROLE; G-CSF; SYNOVIOCYTES; FIBROBLASTS; JNK;

D O I：

10.1136/annrheumdis-2011-200096

中图分类号：

R5 [内科学];

学科分类号：

100201 [内科学];

摘要：

Objectives Interleukin (IL) 34 is a new cytokine implicated in macrophage differentiation and osteoclastogenesis. This study assessed IL-34 expression in the tissue of patients with rheumatoid arthritis (RA). Methods Immunohistochemistry was performed in synovial biopsies from patients with RA (n=20), osteoarthritis (n=3) or other inflammatory arthritis (n=4). IL-34 was detected in the synovial fluid by ELISA and its messenger RNA expression was studied by quantitative PCR in rheumatoid synovial fibroblasts after stimulation by tumour necrosis factor alpha (TNF alpha) and IL-1 beta. Wild-type, jnk1(-/-) -jnk2(-/-) and nemo(-/-) murine fibroblasts and pharmacological inhibition were used to determine the involvement of nuclear factor kappa B (NF-kappa B) and JNK in that effect. Results IL-34 was expressed in 24/27 biopsies, with three samples from RA patients being negative. A significant association was found between IL-34 expression and synovitis severity. Levels of IL-34 and the total leucocyte count in synovial fluid were correlated. TNF alpha and IL-1 beta stimulated IL-34 expression by synovial fibroblasts in a dose/time-dependent manner through the NF-kappa B and JNK pathway. Conclusion This work for the first time identifies IL-34 expression in the synovial tissue of patients with arthritis. This cytokine, as a downstream effector of TNF alpha and IL-1 beta, may contribute to inflammation and bone erosions in RA.

引用

页码：150 / 154

页数：5

共 17 条

[1]

Signal pathways JNK and NF-κB, identified by global gene expression profiling, are involved in regulation of TNFα-induced mPGES-1 and COX-2 expression in gingival fibroblasts [J].