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a Department of Rheumatology and
Immunology, Institute of Medical Science, St Marianna University School
of Medicine, Kawasaki, Japan , b Division of Rheumatology, Nippon
Medical College, Tokyo, Japan
Correspondence to: Dr K Nishioka, Department of Rheumatology and Immunology, Institute of Medical Science, St Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki 216, Japan.
Accepted for publication 27 November 1996
OBJECTIVE
To better understand the
characteristics of synoviocytes located in the rheumatoid arthritis
(RA) pannus.
METHODS
One cell line, termed PSC, was cloned
from RA pannus lesions. Phenotypic analysis was done by contrast
microscopy, indirect immunostaining, and safranin O staining.
Transcription of several protooncogenes and matrix degrading enzymes
was evaluated. The expression of mRNA for collagen II was detected by
in situ hybridisation. The ability of anchorage independent growth was
assessed by soft agarose culture.
RESULTS
PSCs showed a high transcription of
protooncogenes c-fos, c-myc and c-jun. They also expressed mRNA for
matrix degrading enzymes, such as collagenase, cathepsin B, and
cathepsin L. Anchorage independent growth assay demonstrated that PSCs
formed colonies in soft agar culture. Phenotypic analysis showed that
this fibroblast-like PSC was stained intensely with anti-vimentin and
anti-fibroblast antibody. In situ reverse transcriptase assay showed
that the cell line expressed type II collagen mRNA.
CONCLUSION
Alternative fibroblast-like cells
were identified in the pannus lesion of RA sharing properties of
fibroblasts and chondrocytes. These findings suggest that this
fibroblast-like cell derived from pannus lesions may contribute to the
destruction of the cartilage in RA.
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