Role of triggering receptor expressed on myeloid cells-1/3 in Klebsiella-derived pneumosepsis

Am J Respir Cell Mol Biol. 2015 Nov;53(5):647-55. doi: 10.1165/rcmb.2014-0485OC.

Abstract

Triggering receptor expressed on myeloid cells (TREM)-1 and -2 can affect Toll-like receptor-mediated activation of immune cells. Klebsiella pneumoniae is a common cause of pneumonia-derived sepsis. Here we studied the role of TREM-1/3 and TREM-2 in the host response during Klebsiella pneumonia. Macrophages lacking either TREM-1/3 or TREM-2 were tested for their responsiveness toward K. pneumoniae and for their capacity to internalize this pathogen in vitro. TREM-1/3- and TREM-2-deficient mice were infected with K. pneumoniae via the airways, and their responses were compared with those in wild-type mice. TREM-1/3-deficient macrophages produced lower cytokine levels upon exposure to K. pneumoniae, whereas TREM-2-deficient macrophages released higher cytokine concentrations. TREM-2-deficient, but not TREM-1/3-deficient, macrophages showed a reduced capacity to phagocytose K. pneumoniae. TREM-1/3-deficient mice showed an impaired host defense during Klebsiella pneumonia, as reflected by worsened survival and increased bacterial growth and dissemination. In contrast, TREM-2 deficiency did not affect disease outcome. Although TREM-1/3 and TREM-2 influence macrophage responsiveness to K. pneumoniae in vitro, only TREM-1/3 contribute to the host response during Klebsiella pneumonia in vivo, serving a protective role.

Keywords: Klebsiella pneumoniae; TREM-1; TREM-2; macrophages; pneumonia.

MeSH terms

  • Animals
  • Chemokines / genetics
  • Chemokines / immunology
  • Female
  • Gene Expression Regulation
  • Klebsiella pneumoniae / growth & development
  • Klebsiella pneumoniae / immunology
  • Lung / immunology
  • Lung / microbiology
  • Lung / pathology
  • Macrophages, Alveolar / immunology*
  • Macrophages, Alveolar / microbiology
  • Macrophages, Alveolar / pathology
  • Male
  • Membrane Glycoproteins / deficiency
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phagocytosis
  • Pneumonia, Bacterial / genetics
  • Pneumonia, Bacterial / immunology*
  • Pneumonia, Bacterial / microbiology
  • Pneumonia, Bacterial / pathology
  • Primary Cell Culture
  • Receptors, Immunologic / deficiency
  • Receptors, Immunologic / genetics
  • Receptors, Immunologic / immunology*
  • Sepsis / immunology*
  • Sepsis / microbiology
  • Sepsis / pathology
  • Signal Transduction
  • Triggering Receptor Expressed on Myeloid Cells-1
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Chemokines
  • Membrane Glycoproteins
  • Receptors, Immunologic
  • TREM1 protein, mouse
  • Trem2 protein, mouse
  • Trem3 protein, mouse
  • Triggering Receptor Expressed on Myeloid Cells-1
  • Tumor Necrosis Factor-alpha
  • keratinocyte-derived chemokines