Recruitment of osteoclast precursors by stromal cell derived factor-1 (SDF-1) in giant cell tumor of bone

Ted S. Liao, Matthew B. Yurgelun, Seong Sil Chang, Hui Zhu Zhang, Koko Murakami, Theodore A. Blaine, May V. Parisien, William Kim, Robert J. Winchester, Francis Young In Lee

Research output: Contribution to journalArticlepeer-review

71 Scopus citations

Abstract

Giant cell tumor (GCT) of bone is a unique bone lesion that is characterized by an excessive number of multinucleated osteoclasts. GCT consists of neoplastic stromal cells, multinucleated osteoclasts and their precursors, thus serving as a naturally occurring human disease model for the study of osteoclastogenesis. It still remains unclear how stromal cells of GCT recruit osteoclast precursors. In the present study, we characterized the cellular components of GCT and confirmed the presence of CD14+-monocytes/CD68+-macrophages and CD34+-hematopoetic stem cells that express CXCR4, a specific receptor for SDF-1; SDF-1 gene expression and presence of SDF-1 protein were confirmed by real time RT-PCR, in situ hybridization, and immunohistochemistry in the GCT tissue and cultured cells. SDF-1 was present at 25-50 ng/ml in the conditioned media from the GCT cultures, which is in the range of physiological chemotactic concentration. Migration of osteoclast precursors was 2.5-fold higher in response to GCT conditioned media compared to the control media; and migration was inhibited by an average of 36% with anti-SDF-1 neutralizing antibody or competing recombinant SDF-1. These results suggest that SDF-1 is one of the significant chemoattractant factors involved in the recruitment of hematopoietic osteoclast precursor cells during tumor-induced osteoclastogenesis.

Original languageEnglish
Pages (from-to)203-209
Number of pages7
JournalJournal of Orthopaedic Research
Volume23
Issue number1
DOIs
StatePublished - Jan 2005
Externally publishedYes

Keywords

  • Giant cell tumor
  • Osteoclast
  • SDF-1

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