The Role of Transforming Growth Factor β Signaling in Fibroblast-like Synoviocytes From Patients With Oligoarticular Juvenile Idiopathic Arthritis Dysregulation of Transforming Growth Factor β Signaling, Including Overexpression of Bone Morphogenetic Protein 4, May Lead to a Chondrocyte Phenotype and May Contribute to Bony Hypertrophy

被引:32
作者
Brescia, AnneMarie C. [1 ,2 ]
Simonds, Megan M. [3 ]
McCahan, Suzanne M. [3 ]
Fawcett, Paul T. [3 ]
Rose, Carlos D. [1 ,2 ]
机构
[1] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[2] Alfred I DuPont Hosp Children, Nemours, Wilmington, DE 19803 USA
[3] Nemours Biomed Res, Wilmington, DE USA
关键词
RHEUMATOID-ARTHRITIS; CELL-PROLIFERATION; SYNOVIAL TISSUE; STEM-CELLS; EXPRESSION; DIFFERENTIATION; PATHWAY; PREVALENCE; REMISSION; MEMBRANE;
D O I
10.1002/art.38336
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. This study was designed to investigate the pathogenic contributions of fibroblast-like synoviocytes (FLS) to juvenile idiopathic arthritis (JIA) by identifying pathways with dysregulated gene expression in FLS from patients with oligoarticular JIA. Methods. FLS were derived from synovial fluid obtained by arthrocentesis from patients with JIA undergoing intraarticular steroid injections and from orthopedic control patients. Gene expression profiles of the JIA and control FLS were obtained using the Affymetrix platform, with application of Ingenuity Path-way Analysis and Gene Set Enrichment Analysis software to define gene sets in dysregulated pathways and networks of potential pathologic relevance in this disease. Biologically relevant differentially expressed genes were confirmed by RNA and protein analysis. Results. Exploration of global gene expression profiles of the JIA FLS revealed important dysregulated pathways, including the transforming growth factor beta (TGF beta) signaling, as well as endochondral bone formation, cartilage formation, and beta-catenin networks. Importantly, bone morphogenetic protein 4 (BMP-4) was significantly overexpressed in the JIA FLS. FLS from patients with oligoarticular JIA exhibit a chondrocyte phenotype, as evidenced by expression of type II collagen and aggrecan. Conclusion. Dysregulation of the pathways involved in the pathogenesis of oligoarticular JIA were revealed through gene expression profiling. JIA FLS displayed dysregulated TGF beta signaling and exhibited a hypertrophic chondrocyte phenotype. These characteristics, along with contributions from the beta-catenin network may have implications for endochondral bone formation and local growth disturbances in oligoarticular JIA. Overexpression of BMP-4 in FLS from patients with oligoarticular JIA in particular may play an important role in disease pathogenesis, with a direct effect on functional outcome and with implications for future treatment.
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收藏
页码:1352 / 1362
页数:11
相关论文
共 44 条
[1]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[2]  
Bira Yanjmaa, 2005, Mod Rheumatol, V15, P108
[3]   Decrease in expression of bone morphogenetic proteins 4 and 5 in synovial tissue of patients with osteoarthritis and rheumatoid arthritis [J].
Bramlage, Carsten P. ;
Haupl, Thomas ;
Kaps, Christian ;
Ungethum, Ute ;
Krenn, Veit ;
Pruss, Axel ;
Muller, Gerhard A. ;
Strutz, Frank ;
Burmester, Gerd-R .
ARTHRITIS RESEARCH & THERAPY, 2006, 8 (03)
[4]  
BRENNAN FM, 1990, CLIN EXP IMMUNOL, V81, P278
[5]   Wnt/β-catenin signaling in mesenchymal progenitors controls osteoblast and chondrocyte differentiation during vertebrate skeletogenesis [J].
Day, TF ;
Guo, XZ ;
Garrett-Beal, L ;
Yang, YZ .
DEVELOPMENTAL CELL, 2005, 8 (05) :739-750
[6]  
De Bari C, 2001, ARTHRITIS RHEUM-US, V44, P1928, DOI 10.1002/1529-0131(200108)44:8<1928::AID-ART331>3.0.CO
[7]  
2-P
[8]  
Eberhardt K, 1998, BRIT J RHEUMATOL, V37, P1324
[9]   Invasive fibroblast-like synoviocytes in rheumatoid arthritis - Passive responders or transformed aggressors? [J].
Firestein, GS .
ARTHRITIS AND RHEUMATISM, 1996, 39 (11) :1781-1790
[10]   Secreted frizzled related protein 1 regulates Wnt signaling for BMP2 induced chondrocyte differentiation [J].
Gaur, Tripti ;
Rich, Lillian ;
Lengner, Christopher J. ;
Hussain, Sadiq ;
Trevant, Rune ;
Ayers, David ;
Stein, Janet L. ;
Bodine, Peter V. N. ;
Komm, Barry S. ;
Stein, Gary S. ;
Lian, Jane B. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 208 (01) :87-96