Hoxb8 conditionally immortalised macrophage lines model inflammatory monocytic cells with important similarity to dendritic cells

Eur J Immunol. 2011 Feb;41(2):356-65. doi: 10.1002/eji.201040962. Epub 2011 Jan 11.

Abstract

We have examined the potential to generate bona fide macrophages (MØ) from conditionally immortalised murine bone marrow precursors. MØ can be derived from Hoxb8 conditionally immortalised macrophage precursor cell lines (MØP) using either M-CSF or GM-CSF. When differentiated in GM-CSF (GM-MØP) the resultant cells resemble GM-CSF bone marrow-derived dendritic cells (BMDC) in morphological phenotype, antigen phenotype and functional responses to microbial stimuli. In spite of this high similarity between the two cell types and the ability of GM-MØP to effectively present antigen to a T-cell hybridoma, these cells are comparatively poor at priming the expansion of IFN-γ responses from naïve CD4(+) T cells. The generation of MØP from transgenic or genetically aberrant mice provides an excellent opportunity to study the inflammatory role of GM-MØP, and reduces the need for mouse colonies in many studies. Hence differentiation of conditionally immortalised MØPs in GM-CSF represents a unique in vitro model of inflammatory monocyte-like cells, with important differences from bone marrow-derived dendritic cells, which will facilitate functional studies relating to the many 'sub-phenotypes' of inflammatory monocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation / immunology
  • Antigens, Surface / metabolism
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • Cell Differentiation / drug effects
  • Cell Differentiation / immunology*
  • Cell Line, Transformed
  • Cytokines / metabolism
  • Dendritic Cells / cytology*
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Homeodomain Proteins / genetics*
  • Interferon-gamma / metabolism
  • Interleukin-2 / metabolism
  • Lectins, C-Type
  • Lipopeptides / pharmacology
  • Lipopolysaccharides / pharmacology
  • Macrophage Colony-Stimulating Factor / pharmacology
  • Macrophages / cytology*
  • Macrophages / drug effects
  • Macrophages / immunology
  • Macrophages / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, 129 Strain
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Mice, Knockout
  • Monocyte-Macrophage Precursor Cells / cytology*
  • Monocyte-Macrophage Precursor Cells / drug effects
  • Monocyte-Macrophage Precursor Cells / metabolism
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Nitric Oxide / metabolism
  • Ovalbumin / immunology
  • Transduction, Genetic
  • Zymosan / pharmacology
  • beta-Glucans / pharmacology

Substances

  • Antigens, Surface
  • Cytokines
  • Homeodomain Proteins
  • Hoxb8 protein, mouse
  • Interleukin-2
  • Lectins, C-Type
  • Lipopeptides
  • Lipopolysaccharides
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Pam(3)CSK(4) peptide
  • beta-Glucans
  • dectin 1
  • Nitric Oxide
  • curdlan
  • Macrophage Colony-Stimulating Factor
  • Interferon-gamma
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Ovalbumin
  • Zymosan