Regulation of granulocyte and macrophage populations of murine bone marrow cells by G-CSF and CD137 protein

PLoS One. 2010 Dec 13;5(12):e15565. doi: 10.1371/journal.pone.0015565.

Abstract

Background: Granulocytes and monocytes/macrophages differentiate from common myeloid progenitor cells. Granulocyte colony-stimulating factor (G-CSF) and CD137 (4-1BB, TNFRSF9) are growth and differentiation factors that induce granulocyte and macrophage survival and differentiation, respectively. This study describes the influence of G-CSF and recombinant CD137-Fc protein on myelopoiesis.

Methodology/principal findings: Both, G-CSF and CD137 protein support proliferation and survival of murine bone marrow cells. G-CSF enhances granulocyte numbers while CD137 protein enhances macrophage numbers. Both growth factors together give rise to more cells than each factor alone. Titration of G-CSF and CD137 protein dose-dependently changes the granulocyte/macrophage ratio in bone marrow cells. Both factors individually induce proliferation of hematopoietic progenitor cells (lin-, c-kit+) and differentiation to granulocytes and macrophages, respectively. The combination of G-CSF and CD137 protein further increases proliferation, and results in a higher number of macrophages than CD137 protein alone, and a lower number of granulocytes than G-CSF alone demonstrating that CD137 protein-induced monocytic differentiation is dominant over G-CSF-induced granulocytic differentiation. CD137 protein induces monocytic differentiation even in early hematopoietic progenitor cells, the common myeloid progenitors and the granulocyte macrophage progenitors.

Conclusions/significance: This study confirms earlier data on the regulation of myelopoiesis by CD137 receptor - ligand interaction, and extends them by demonstrating the restriction of this growth promoting influence to the monocytic lineage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Bone Marrow Cells / cytology*
  • CD11b Antigen / biosynthesis
  • Cell Differentiation
  • Esterases / metabolism
  • Female
  • Flow Cytometry / methods
  • Granulocyte Colony-Stimulating Factor / metabolism*
  • Granulocytes / cytology*
  • Hematopoietic Stem Cells / cytology
  • Macrophages / cytology*
  • Mice
  • Mice, Inbred BALB C
  • Recombinant Proteins / metabolism
  • Tumor Necrosis Factor Receptor Superfamily, Member 9 / metabolism*

Substances

  • CD11b Antigen
  • Recombinant Proteins
  • Tumor Necrosis Factor Receptor Superfamily, Member 9
  • Granulocyte Colony-Stimulating Factor
  • Esterases