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Logo of arthresbiomed central web sitesearch.manuscript submission.see also journal with issn 1478-6354registration.reference to the article.journal front page.
Arthritis Res. 2001; 3(Suppl A): P095.
Published online Jan 26, 2001. doi:  10.1186/ar264
PMCID: PMC3273268
Induction of a rapid progessive cartilage destruction in SCID mice by intraarticular application of a murine fibroblast like cell line
U Sack,1 A Hirth,1 B Funke,1 K Wiedemeyer,1 S Konrad,1 J Lehmann,1 and F Emmrich1
1Institute of Clinical Immunology and Transfusion Medicine, University of Leipzig, Germany
21st European Workshop for Rheumatology Research
21st European Workshop for Rheumatology Research
1-4 March 2001
Vienna, Austria
Received January 15, 2001
In pathogenesis of rheumatoid arthritis, fibroblasts are considered to be a crucial cell population for disease progression as well as joint destruction. Following intraarticular injection into SCID mice, isolated human rheumatoid synovial fibroblasts have been shown to induce a destructive arthritis (hu/mu SCID arthritis). Although exclusively human synovial fibroblasts were able to induce this arthritis, cartilage destruction was caused by murine fibroblast like cells in this model. Therefore, we have isolated a murine destructive fibroblastoid cell line and established a cartilage destruction model.
Material and methods
LS48 cell line was examined for morphological, ultrastructural, immunological, and functional parameters. Furthermore, cartilage destruction was induced by intraarticular application of LS48 cells into SCID mouse knee joints. Mice were monitored for joint swelling, serological parameters and by radiological methods. Finally, immunohistochemistry and histology were used to characterize morphology of cartilage destruction.
LS48 was shown to present characteristics of a fibroblast-like cell. Secretion of interleukin-6 and tumor necrosis factor-alpha revealed similarities to human invasive rheumatoid synovial membrane fibroblasts. Installation of 5 × 105 cells into SCID mouse knee joints caused a rapid progressive process causing cartilage destruction within 10 days. Morphology revealed infiltration of fibroblast like cells into the cartilage.
Induction of cartilage destruction by intraarticular application of these murine fibroblast like cells is a rapid and highly reproducible model for investigation of cartilage destruction in arthritic joints. This provides an excellent possibility to investigate relevant processes and new therapeutic strategies for rheumatoid arthritis in an easy-to-handle animal model.
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