M-CSF increases proliferation and phagocytosis while modulating receptor and transcription factor expression in adult human microglia

J Neuroinflammation. 2013 Jul 17:10:85. doi: 10.1186/1742-2094-10-85.

Abstract

Background: Microglia are the primary immune cells of the brain whose phenotype largely depends on their surrounding micro-environment. Microglia respond to a multitude of soluble molecules produced by a variety of brain cells. Macrophage colony-stimulating factor (M-CSF) is a cytokine found in the brain whose receptor is expressed by microglia. Previous studies suggest a critical role for M-CSF in brain development and normal functioning as well as in several disease processes involving neuroinflammation.

Methods: Using biopsy tissue from patients with intractable temporal epilepsy and autopsy tissue, we cultured primary adult human microglia to investigate their response to M-CSF. Mixed glial cultures were treated with 25 ng/ml M-CSF for 96 hours. Proliferation and phagocytosis assays, and high through-put immunocytochemistry, microscopy and image analysis were performed to investigate microglial phenotype and function.

Results: We found that the phenotype of primary adult human microglia was markedly changed following exposure to M-CSF. A greater number of microglia were present in the M-CSF- treated cultures as the percentage of proliferating (BrdU and Ki67-positive) microglia was greatly increased. A number of changes in protein expression occurred following M-CSF treatment, including increased transcription factors PU.1 and C/EBPβ, increased DAP12 adaptor protein, increased M-CSF receptor (CSF-1R) and IGF-1 receptor, and reduced HLA-DP, DQ, DR antigen presentation protein. Furthermore, a distinct morphological change was observed with elongation of microglial processes. These changes in phenotype were accompanied by a functional increase in phagocytosis of Aβ1-42 peptide.

Conclusions: We show here that the cytokine M-CSF dramatically influences the phenotype of adult human microglia. These results pave the way for future investigation of M-CSF-related targets for human therapeutic benefit.

MeSH terms

  • Adaptor Proteins, Signal Transducing / biosynthesis
  • Adaptor Proteins, Signal Transducing / genetics
  • Antimetabolites
  • Autopsy
  • Biopsy
  • Bromodeoxyuridine
  • CCAAT-Enhancer-Binding Protein-beta / biosynthesis
  • Cell Proliferation / drug effects*
  • Cells, Cultured
  • HLA Antigens / biosynthesis
  • Humans
  • Image Processing, Computer-Assisted
  • Immunohistochemistry
  • Ki-67 Antigen / metabolism
  • Macrophage Activation / drug effects
  • Macrophage Colony-Stimulating Factor / pharmacology*
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / genetics
  • Microglia / drug effects*
  • Microglia / metabolism
  • Phagocytosis / drug effects*
  • Proto-Oncogene Proteins / biosynthesis
  • Proto-Oncogene Proteins / genetics
  • Receptor, Macrophage Colony-Stimulating Factor / biosynthesis
  • Trans-Activators / biosynthesis
  • Trans-Activators / genetics
  • Transcription Factors / biosynthesis*

Substances

  • Adaptor Proteins, Signal Transducing
  • Antimetabolites
  • CCAAT-Enhancer-Binding Protein-beta
  • HLA Antigens
  • Ki-67 Antigen
  • Membrane Proteins
  • Proto-Oncogene Proteins
  • TYROBP protein, human
  • Trans-Activators
  • Transcription Factors
  • proto-oncogene protein Spi-1
  • Macrophage Colony-Stimulating Factor
  • Receptor, Macrophage Colony-Stimulating Factor
  • Bromodeoxyuridine