Transition of healthy to diseased synovial tissue in rheumatoid arthritis is associated with gain of mesenchymal/fibrotic characteristics

• Published in: Arthritis research & therapy 2006-01, Vol.8 (6), p.R165-R165, Article R165
• Main Authors: Steenvoorden, Marjan M C, Tolboom, Tanja C A, van der Pluijm, Gabri, Löwik, Clemens, Visser, Cornelis P J, DeGroot, Jeroen, Gittenberger-DeGroot, Adriana C, DeRuiter, Marco C, Wisse, Bert J, Huizinga, Tom W J, Toes, René E M
• Format: Article
• Language: English
• Subjects: Actins - biosynthesis; Arthritis, Rheumatoid - metabolism; Arthritis, Rheumatoid - pathology; Bone Morphogenetic Protein 7; Bone Morphogenetic Proteins - metabolism; Cadherins - biosynthesis; Collagen Type IV - biosynthesis; Disease Progression; Fibroblasts - cytology; Fibroblasts - metabolism; Fibrosis - pathology; Humans; Immunohistochemistry; Mesoderm - pathology; Reverse Transcriptase Polymerase Chain Reaction; Synovial Membrane - cytology; Synovial Membrane - pathology; Transforming Growth Factor beta - metabolism
• ISSN: 1478-6354; 1478-6362; 1478-6354
• DOI: 10.1186/ar2073

The healthy synovial lining layer consists of a single cell layer that regulates the transport between the joint cavity and the surrounding tissue. It has been suggested that abnormalities such as somatic mutations in the p53 tumor-suppressor gene contribute to synovial hyperplasia and invasion in rheumatoid arthritis (RA). In this study, expression of epithelial markers on healthy and diseased synovial lining tissue was examined. In addition, we investigated whether a regulated process, resembling epithelial to mesenchymal transition (EMT)/fibrosis, could be responsible for the altered phenotype of the synovial lining layer in RA. Synovial tissue from healthy subjects and RA patients was obtained during arthroscopy. To detect signs of EMT, expression of E-cadherin (epithelial marker), collagen type IV (indicator of the presence of a basement membrane) and alpha-smooth muscle actin (alpha-sma; a myofibroblast marker) was investigated on frozen tissue sections using immunohistochemistry. Fibroblast-like synoviocytes (FLSs) from healthy subjects were isolated and subjected to stimulation with synovial fluid (SF) from two RA patients and to transforming growth factor (TGF)-beta. To detect whether EMT/fibrotic markers were increased, expression of collagen type I, alpha-sma and telopeptide lysylhydroxylase (TLH) was measured by real time PCR. Expression of E-cadherin and collagen type IV was found in healthy and arthritic synovial tissue. Expression of alpha-sma was only found in the synovial lining layer of RA patients. Stimulation of healthy FLSs with SF resulted in an upregulation of alpha-sma and TLH mRNA. Collagen type I and TLH mRNA were upregulated after stimulation with TGF-beta. Addition of bone morphogenetic protein (BMP)-7 to healthy FLS stimulated with SF inhibited the expression of alpha-sma mRNA. The finding that E-cadherin and collagen type IV are expressed in the lining layer of healthy and arthritic synovium indicates that these lining cells display an epithelial-like phenotype. In addition, the presence of alpha-sma in the synovial lining layer of RA patients and induction of fibrotic markers in healthy FLSs by SF from RA patients indicate that a regulated process comparable to EMT might cause the alteration in phenotype of RA FLSs. Therefore, BMP-7 may represent a promising agent to counteract the transition imposed on synoviocytes in the RA joint.