Mechanisms involved in the differential bone marrow homing of CD45 subsets in 5T murine models of myeloma

Clin Exp Metastasis. 2002;19(7):583-91. doi: 10.1023/a:1020987830132.

Abstract

Multiple myeloma (MM) is an incurable plasma cell cancer, localized in the bone marrow (BM). The mechanisms used by these cells to (re-)enter this organ remain largely unknown. Recently, we reported that both CD45+ and CD45- myeloma cells home to the BM and induce myeloma disease. In this work, we investigated the underlying mechanisms involved in the homing of CD45+ and CD45- myeloma cells in the experimental 5T2MM and 5T33MM murine models. In vivo tracing of flow cytometric sorted and radioactively labeled CD45 subsets revealed a reduced homing of the CD45- 5TMM cells to the BM as compared to the CD45+ 5TMM cells. Migration assays demonstrated an impaired chemotaxis towards BM endothelial cell conditioned medium, BM stromal cell conditioned medium and towards the basement membrane component laminin-1 of the CD45- 5TMM cells compared to the CD45+ subset. Matrix metalloproteinase-9 (MMP-9) and urokinase type plasminogen activator (uPA) are key extracellular matrix proteases involved in the invasion of cancer cells. Inhibitor and antibody blocking experiments demonstrated the involvement of both in the invasion of the 5TMM cells. CD45- 5TMM cells had a low secretion of MMP-9 and (for the non-aggressive line 5T2MM only) a low cell surface expression of uPA receptor, as revealed by gelatin zymography and flow cytometric analysis, respectively. Accordingly, the synthetic basement membrane invasive capacity of the CD45- 5TMM subpopulations was also impaired. Our results indicate that CD45+ and CD45- 5T myeloma cells have a differential BM homing attributable to differential migratory and invasive capacities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow / drug effects
  • Bone Marrow / immunology*
  • Bone Marrow / pathology
  • Catechin / analogs & derivatives*
  • Catechin / pharmacology
  • Cell Adhesion / drug effects
  • Cells, Cultured
  • Chemotaxis / drug effects
  • Endothelium / cytology
  • Endothelium / metabolism
  • Fibroblasts / metabolism
  • Fibroblasts / pathology
  • Laminin / metabolism
  • Leukocyte Common Antigens / drug effects
  • Leukocyte Common Antigens / metabolism*
  • Male
  • Matrix Metalloproteinase 9 / metabolism
  • Matrix Metalloproteinase Inhibitors
  • Mice
  • Mice, Inbred C57BL
  • Multiple Myeloma / drug therapy
  • Multiple Myeloma / immunology*
  • Multiple Myeloma / pathology*
  • Neoplasm Invasiveness
  • Neoplasms, Experimental
  • Protease Inhibitors / pharmacology
  • Receptors, Cell Surface / drug effects
  • Receptors, Cell Surface / metabolism
  • Receptors, Urokinase Plasminogen Activator
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / metabolism*
  • Urokinase-Type Plasminogen Activator / antagonists & inhibitors
  • Urokinase-Type Plasminogen Activator / metabolism

Substances

  • Laminin
  • Matrix Metalloproteinase Inhibitors
  • Plaur protein, mouse
  • Protease Inhibitors
  • Receptors, Cell Surface
  • Receptors, Urokinase Plasminogen Activator
  • laminin 1
  • Catechin
  • epigallocatechin gallate
  • Leukocyte Common Antigens
  • Urokinase-Type Plasminogen Activator
  • Matrix Metalloproteinase 9