Phenotypic and functional modulations of porcine macrophages by interferons and interleukin-4

Dev Comp Immunol. 2018 Jul:84:181-192. doi: 10.1016/j.dci.2018.01.018. Epub 2018 Jan 31.

Abstract

Considering that macrophage functions are strongly impacted by the local tissue environment and the type of immune response, the aim of this study was to carefully set the methodological baseline for phenotype and functions of polarized porcine monocyte-derived macrophages. To this end, macrophages were generated in autologous serum alone or with colony-stimulating factor (CSF)-1 or CSF-2, and subsequently polarized with interferon (IFN)γ, interleukin-4 or IFNβ. IFNγ promoted expression of MHC class I, MHC class II, CD11a, and CD40 as well as LPS-induced IL-6 and IL-12. A hallmark of interleukin-4 was Arginase 1 and CD203a upregulation, without abrogating pro-inflammatory cytokine production. IFNβ induced CD169, MHC class I, CD40, CD80/86, but suppressed IL-6, IL-12 and tumor-necrosis-factor secretion. CSF-2 alone altered macrophage differentiation and promoted an IFNγ-like polarization. Altogether, the results provide a comprehensive overview of porcine macrophage polarization, and demonstrate commonalities with other species as well as peculiarities of the pig.

Keywords: IFNβ; IFNγ; IL-4; Macrophages; Pig; Polarization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Arginase / metabolism
  • Cell Differentiation
  • Cells, Cultured
  • Colony-Stimulating Factors / metabolism
  • Cytokines / metabolism
  • Histocompatibility Antigens / metabolism
  • Immunophenotyping
  • Inflammation Mediators / metabolism
  • Interferon-beta / metabolism*
  • Interferon-gamma / metabolism*
  • Interleukin-4 / metabolism
  • Macrophages / immunology*
  • Monocytes / immunology*
  • Species Specificity
  • Swine / immunology*

Substances

  • Antigens, CD
  • Colony-Stimulating Factors
  • Cytokines
  • Histocompatibility Antigens
  • Inflammation Mediators
  • Interleukin-4
  • Interferon-beta
  • Interferon-gamma
  • Arginase