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  • Oral presentation
  • Open Access

Overview of osteoimmunology: What's happened? And what's going on?

  • 1
Arthritis Research & Therapy201214 (Suppl 1) :O12

  • Published:


  • Public Health
  • Transcription Factor
  • Arthritis
  • Molecular Mechanism
  • Bone Formation

The interaction between the immune and skeletal systems has long been acknowledged, but molecular mechanisms linking the two systems have not been demonstrated until recently. Investigation into autoimmune arthritis as well as the various bone phenotypes found in mice deficient in immunomodulatory molecules has highlighted the importance of the dynamic interplay between the two systems and brought about a rapid evolution of the field of osteoimmunology [1]. In bone loss in autoimmune arthritis, IL-17-producing helper T (TH17) cells play a major role by inducing RANKL [2]. Maintenance and mobilization of hematopoietic cells are regulated by bone cells. In addition to cellular interactions via cytokines, the immune and skeletal systems share various molecules, including transcription factors, signaling molecules and membrane receptors. RANKL stimulates osteoclastogenesis through NFATc1 in cooperation with immunoglobulin-like receptors. Here I will discuss emerging topics in osteoimmunology including the mechanisms underlying bone cell communication: osteocyte RANKL [3] and inhibition of bone formation by osteoclast Sema4D [4].

Authors’ Affiliations

ERATO, Tokyo Medical and Dental University, Japan


  1. Nat Rev Immunol. 2007, 7: 292-304.Google Scholar
  2. Nat Rev Rheumatol. 2009, 5: 667-76.Google Scholar
  3. Nat Med. 2011, 17: 1231-34.Google Scholar
  4. Nat Med. 2011, 17: 1473-80.Google Scholar


© Takayanagi; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.