The interaction of human natural killer cells with either unpolarized or polarized macrophages results in different functional outcomes

Proc Natl Acad Sci U S A. 2010 Dec 14;107(50):21659-64. doi: 10.1073/pnas.1007654108. Epub 2010 Nov 30.

Abstract

The cross-talk among cells of the innate immunity can greatly affect both innate and adaptive responses. Here we analyzed the molecular interactions between human natural killer (NK) cells and autologous macrophages. Activated NK cells killed M0 and M2, whereas M1 macrophages were more resistant to lysis because of their higher expression of HLA class I molecules. Following exposure to LPS or bacillus Calmette-Guérin, M0 and M2, but not polarized (endotoxin tolerant) M1 macrophages, induced strong activation of resting NK cells. The expression of CD69 and CD25 activation markers and the acquisition of cytotoxicity against tumor cells and immature dendritic cells required soluble factors being mostly contact independent. On the contrary, IFN-γ production was contact dependent and required the interaction of DNAM-1 and 2B4 (on NK) with their ligands on macrophages as well as IL-18. IL-18 was involved also in the acquisition of CCR7 by NK cells. Interestingly, M0 and M2 cells expressed a membrane-bound form of IL-18, which was released in small amounts after LPS treatment. Our data indicate that, upon interaction with M0 macrophages exposed to microbial products, NK cells may amplify classical type 1 immune responses. In addition, M1-polarizing stimuli can rescue M2 macrophages from their immunomodulatory state and shape their functional behavior toward NK stimulatory capability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / immunology
  • Antigens, Differentiation, T-Lymphocyte / immunology
  • Cell Polarity*
  • Cells, Cultured
  • Coculture Techniques
  • Cytokines / immunology
  • Genes, MHC Class I
  • Humans
  • Interleukin-2 Receptor alpha Subunit / immunology
  • K562 Cells
  • Killer Cells, Natural / cytology
  • Killer Cells, Natural / immunology*
  • Lectins, C-Type / immunology
  • Lipopolysaccharides / immunology
  • Lipopolysaccharides / pharmacology
  • Lymphocyte Activation / immunology
  • Macrophages / cytology
  • Macrophages / drug effects
  • Macrophages / immunology*
  • Receptors, CCR7 / immunology

Substances

  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • CCR7 protein, human
  • CD69 antigen
  • Cytokines
  • IL2RA protein, human
  • Interleukin-2 Receptor alpha Subunit
  • Lectins, C-Type
  • Lipopolysaccharides
  • Receptors, CCR7