Macrophage migration inhibitory factor enhances osteoclastogenesis through upregulation of RANKL expression from fibroblast-like synoviocytes in patients with rheumatoid arthritis
2011

MIF and Its Role in Bone Destruction in Rheumatoid Arthritis

Sample size: 16 publication Evidence: moderate

Author Information

Author(s): Kim Hae-Rim, Kim Kyoung-Woon, Jung Hong Geun, Yoon Kwang-Sup, Oh Hye-Jwa, Cho Mi-La, Lee Sang-Heon

Primary Institution: Konkuk University School of Medicine

Hypothesis

MIF may play an important role in the process of bone destruction in RA patients through the induction of RANKL or direct involvement of osteoclastogenesis.

Conclusion

MIF enhances osteoclastogenesis by upregulating RANKL expression in rheumatoid arthritis patients.

Supporting Evidence

  • MIF concentration in RA patients was significantly higher than in OA patients.
  • The concentration of RANKL correlated with that of MIF in RA synovial fluids.
  • MIF stimulated the expression of RANKL mRNA and protein in RA synovial fibroblasts.

Takeaway

MIF is a protein that helps cells in the body called osteoclasts break down bone, which is important in diseases like rheumatoid arthritis.

Methodology

The study measured MIF and RANKL concentrations in synovial fluid and analyzed osteoclastogenesis using human peripheral blood mononuclear cells.

Participant Demographics

16 RA patients, mean age 63.4 ± 4.6 years.

Statistical Information

P-Value

<0.001

Statistical Significance

p<0.001

Digital Object Identifier (DOI)

10.1186/ar3279

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