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Updated: Apr 5, 2026

Application of Atomic Force Microscopy to Detect Early Osteoarthritis
Published on: May 24, 2020
Detecting changes in arthritic fibroblast-like synoviocytes using atomic force microscopy
Jee-Wook Lee1, Myoung-Ryul Ok2, Sangmook Lee3
1School of Advanced Materials Engineering, Kookmin University, Seoul, Korea.
Atomic force microscopy (AFM) reveals distinct surface roughness in arthritic fibroblast-like synoviocytes (FLS) compared to normal FLS. This difference offers a potential diagnostic tool for early rheumatoid arthritis (RA) detection at the cellular level.
Area of Science:
- Biomedical Engineering
- Rheumatology
- Cell Biology
Background:
- Rheumatoid arthritis (RA) diagnosis relies on identifying specific cellular changes.
- Fibroblast-like synoviocytes (FLS) play a crucial role in RA pathogenesis.
- Quantitative morphological analysis of FLS can offer diagnostic insights.
Purpose of the Study:
- To investigate morphological and quantitative differences between arthritic and normal FLS.
- To evaluate the potential of atomic force microscopy (AFM) as a diagnostic tool for RA.
- To correlate FLS surface roughness with RA pathogenesis duration.
Main Methods:
- Fibroblast-like synoviocytes (FLS) were isolated from collagen-induced arthritic (CIA) mice and normal mice.
- Synovial tissue samples were collected at 5-week and 8-week pathogenesis periods.
- Atomic force microscopy (AFM) was used to analyze FLS surface roughness.
Main Results:
- Arthritic FLS exhibited significantly higher surface roughness around the nucleus and cytoplasm compared to normal FLS (P < 0.05).
- The surface roughness of arthritic FLS increased with the duration of RA pathogenesis.
- AFM demonstrated quantifiable differences in FLS morphology between arthritic and normal states.
Conclusions:
- AFM can effectively differentiate between arthritic and normal FLS based on surface roughness.
- AFM shows promise as a diagnostic tool for early RA detection at the intercellular level.
- This technique may be applicable for diagnosing other intercellular diseases.
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