International Orthopaedics

, Volume 38, Issue 1, pp 183–192 | Cite as

Association of systemic and intra-articular osteoclastogenic potential, pro-inflammatory mediators and disease activity with the form of inflammatory arthritis

  • Marina Ikić
  • Zrinka Jajić
  • Elvira Lazić
  • Sanja Ivčević
  • Frane Grubišić
  • Ana Marušić
  • Nataša Kovačić
  • Danka Grčević
Original Paper

Abstract

Purpose

We aimed to assess osteoclastogenic potential of peripheral blood mononuclear cells (PBMC) and synovial fluid-derived mononuclear cells (SFMC) in different forms of arthritis and to correlate it with inflammatory mediators within intra-articular and circulatory compartments.

Methods

Paired PBMC and SFMC samples of patients with rheumatoid arthritis (RA; n = 10) and psoriatic arthritis (PsA; n = 10), and PBMC of healthy controls were cultured to assess osteoclastogenic potential by the number of tartrate-resistant acid phosphatase (TRAP)-positive osteoclasts (OCs) and expression of OC-related genes (receptor activator of nuclear factor-κΒ (RANK), cFMS, and TRAP). Osteoclastogenesis was correlated with the arthritis-related inflammatory indicators in serum and synovial fluid (SF).

Results

Number of OCs differentiated from PBMC was significantly higher in RA and PsA compared with control, with RA having more OCs compared with PsA. There was no difference in SFMC OC number between arthritic patients, but RANK expression in OCs differentiated from SFMC was higher in PsA compared with RA. SF of PsA patients more potently induced OC differentiation from control CD3-CD19-CD56-CD11b+CD115+ PBMC compared with RA, paralleled with higher RANK-ligand expression in PsA SFMC. Positive correlations of OC number with erythrocyte sedimentation rate, serum level of CCL2, and PBMC gene expression of interleukin-18 and Fas-ligand were observed.

Conclusion

Osteoclastogenic potential is systemically enhanced in patients with RA, paralleled by disordered systemic and local expression of proinflammatory mediators, whereas PsA involves specific deregulation in RANKL/RANK axis. Our study reveals arthritis-specific mediators associated with the form of arthritis, indicating clinical relevance for diagnosis and treatment.

Keywords

Rheumatoid arthritis Psoriatic arthritis Osteoclasts Cytokines Inflammation Bone loss Peripheral blood Synovial fluid 

Notes

Acknowledgments

This work was supported by grants from the Croatian Ministry of Science, Education and Sports (108-1080229-0140, 108-1080229-0142, and 108-1080229-0341).

We thank Prof. Vedran Katavic for critically revising the manuscript and Mrs. Katerina Zrinski-Petrovic for her technical assistance.

Conflict of interest

The authors declare that they have no conflict of interest.

Supplementary material

264_2013_2121_MOESM1_ESM.docx (17 kb)
Supplementary Table 1 (DOCX 17.3 kb)
264_2013_2121_MOESM2_ESM.docx (14 kb)
Supplementary Table 2 (DOCX 14 kb)

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Copyright information

© Springer-Verlag Berlin Heidelberg 2013

Authors and Affiliations

  • Marina Ikić
    • 1
    • 2
  • Zrinka Jajić
    • 3
  • Elvira Lazić
    • 4
  • Sanja Ivčević
    • 1
  • Frane Grubišić
    • 3
  • Ana Marušić
    • 5
  • Nataša Kovačić
    • 1
  • Danka Grčević
    • 1
    • 6
  1. 1.Laboratory for Molecular ImmunologyUniversity of Zagreb School of MedicineZagrebCroatia
  2. 2.Department of Clinical Immunology and RheumatologyUniversity Hospital “Holy Ghost”, University of Zagreb School of MedicineZagrebCroatia
  3. 3.Department of Rheumatology, Physical Medicine and RehabilitationClinical Hospital Center “Sisters of Mercy”, University of Zagreb School of MedicineZagrebCroatia
  4. 4.Department of Dermatology and VenereologyGeneral Hospital “Dr. Ivo Pedišić”SisakCroatia
  5. 5.Department of Research in Biomedicine and HealthUniversity of Split School of MedicineSplitCroatia
  6. 6.Department of Physiology and ImmunologyUniversity of Zagreb School of MedicineZagrebCroatia

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