IL-3 expression by myeloma cells increases both osteoclast formation and growth of myeloma cells

Blood. 2004 Mar 15;103(6):2308-15. doi: 10.1182/blood-2003-06-1992. Epub 2003 Nov 13.

Abstract

Macrophage inflammatory protein-1 alpha (MIP-1 alpha) gene expression is abnormally regulated in multiple myeloma (MM) owing to imbalanced expression of the acute myeloid leukemia-1A (AML-1A) and AML-1B transcription factors. We hypothesized that the increased expression ratios of AML-1A to AML-1B also induced abnormal expression of other hematopoietic and bone-specific genes that contribute to the poor prognosis of MM patients with high levels of MIP-1 alpha. We found that interleukin-3 (IL-3) was also induced by the imbalanced AML-1A and AML-1B expression in myeloma. IL-3 mRNA levels were increased in CD138+ purified myeloma cells with increased AML-1A-to-AML-1B expression from MM patients, and IL-3 protein levels were significantly increased in freshly isolated bone marrow plasma from MM patients (66.4 +/- 12 versus 22.1 +/- 8.2 pg/mL; P = .038). IL-3 in combination with MIP-1 alpha or receptor activator of nuclear factor-kappa B ligand (RANKL) significantly enhanced human osteoclast (OCL) formation and bone resorption compared with MIP-1 alpha or RANKL alone. IL-3 stimulated the growth of interleukin-6 (IL-6)-dependent and IL-6-independent myeloma cells in the absence of IL-6, even though IL-3 did not induce IL-6 expression by myeloma cells. These data suggest that increased IL-3 levels in the bone marrow microenvironment of MM patients with imbalanced AML-1A and AML-1B expression can increase bone destruction and tumor cell growth.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Antibodies / pharmacology
  • Bone Marrow Cells / physiology
  • Bone Resorption / physiopathology
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cell Differentiation / physiology
  • Cell Division / physiology
  • Cell Line, Tumor
  • Chemokine CCL4
  • Core Binding Factor Alpha 2 Subunit
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Down-Regulation
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Interleukin-3 / genetics*
  • Interleukin-3 / immunology
  • Macrophage Inflammatory Proteins / genetics
  • Macrophage Inflammatory Proteins / metabolism
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Multiple Myeloma / pathology*
  • Multiple Myeloma / physiopathology*
  • Osteoclasts / cytology*
  • Osteoclasts / physiology*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • RANK Ligand
  • RNA, Messenger / analysis
  • Receptor Activator of Nuclear Factor-kappa B
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transfection

Substances

  • Antibodies
  • Carrier Proteins
  • Chemokine CCL4
  • Core Binding Factor Alpha 2 Subunit
  • DNA-Binding Proteins
  • Interleukin-3
  • Macrophage Inflammatory Proteins
  • Membrane Glycoproteins
  • Proto-Oncogene Proteins
  • RANK Ligand
  • RNA, Messenger
  • RUNX1 protein, human
  • Receptor Activator of Nuclear Factor-kappa B
  • TNFRSF11A protein, human
  • TNFSF11 protein, human
  • Transcription Factors