Interdependence between cytokines and cell adhesion molecules to induce interleukin-6 production by stromal cells in myeloma

Leuk Lymphoma. 1998 Dec;32(1-2):107-19. doi: 10.3109/10428199809059251.

Abstract

Bone marrow (BM) environment is thought to support the growth of myeloma cells and thus to play an important role in the pathogenesis of multiple myeloma (MM). Because interleukin-6 (IL-6) is an essential growth factor in MM, we have examined the effects of two myeloma cell lines (U266 and ARH-77) on the IL-6 production by BM stromal cells in a co-culture system. These cell lines strongly stimulate the IL-6 production and IL-6 triggering was partially dependent on physical contact between lines and stroma. The percentages of cell adhesion to stromal layers were 39% and 25% respectively for ARH77 and U266 cell lines. Inhibition studies with blocking monoclonal antibodies showed the importance of CD49d/CD106 and CD11a/CD54 interactions in the stimulation of IL-6 production by stromal cells. However, cell-to-cell contact was not an absolute requirement for IL-6 production. Cytokines, of which TNF-alpha and IL-1beta produced by MM or accessory cells, were also able to stimulate IL-6 production by fibroblasts and show additive effects. In adhesion assays, TNF-alpha and IL-1beta were able to increase the adhesion of MM cells to stromal cells. CD54 was upregulated by IL-1beta, TNF-alpha or a contact with MM cells while CD106 expression was not, suggesting only a functional change of this molecule. However, the role of monoclonal antibodies, directed against these factors, confirmed the role of TNF-alpha in the IL-6 production by stromal cells, while any IL-1beta intervention was not shown in our co-culture system. IL-6 favoured and maintained adhesion of MM cells to stromal cells spontaneously since its reintroduction in the favoured co-culture system restored their decreased adhesion observed on a glutaraldehyde fixed stromal layer. Overall our data suggest a functional overlap between cytokines and adhesion molecules for the paracrine IL-6 production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / pharmacology
  • Antigens, CD / immunology
  • Binding, Competitive
  • Cell Adhesion / drug effects
  • Cell Adhesion Molecules / metabolism*
  • Cells, Cultured
  • Coculture Techniques
  • Cytokines / pharmacology*
  • Extracellular Matrix Proteins / immunology
  • Extracellular Matrix Proteins / metabolism
  • Humans
  • Interleukin-1 / immunology
  • Interleukin-1 / pharmacology
  • Interleukin-6 / biosynthesis*
  • Multiple Myeloma / metabolism*
  • Multiple Myeloma / pathology
  • Stromal Cells / cytology
  • Stromal Cells / metabolism*
  • Time Factors
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / pharmacology
  • Up-Regulation / drug effects

Substances

  • Antibodies
  • Antigens, CD
  • Cell Adhesion Molecules
  • Cytokines
  • Extracellular Matrix Proteins
  • Interleukin-1
  • Interleukin-6
  • Tumor Necrosis Factor-alpha