IL-17 contributes to the pathogenesis of obliterative bronchiolitis via regulation of M1 macrophages polarization in murine heterotopic trachea transplantation models

Int Immunopharmacol. 2017 Nov:52:51-60. doi: 10.1016/j.intimp.2017.08.022. Epub 2017 Aug 31.

Abstract

Acute allograft rejection is a principal conundrum in lung obliterative bronchiolitis (OB). Monocytes/macrophages infiltration has been proved to be the main reason for acute rejection. IL-17 contributes to the recruitment and function of macrophages. However, the mechanism of IL-17 underlying OB progression remains elusive. In the present study, we showed that the deficiency of IL-17 attenuated the pathology of murine heterotopic trachea allografts. Compared to WT recipients, IL-17-/- mice displayed higher frequency of CD206+ cells and lower ratio of CD86+ cells among F4/80+ macrophages in allografts and spleens on day 7 post heterotopic trachea transplantation. Moreover, mRNA levels of pro-inflammatory cytokines including IL-6, TNF-α, and IL-1β decreased in allografts of IL-17-/- recipients, but these of MRC1 and Arg-1 increased in comparison with WT. IL-17 deficiency can inhibit LPS induced M1 while promote IL-4 induced M2 polarization of bone marrow-derived macrophages. Further data demonstrated that the deficiency of IL-17 suppressed the lipopolysaccharide-induced M1 polarization and function through prevention of phosphorylation of both STAT3 and STAT5. Therefore, IL-17 contributes to OB pathogenesis through regulating macrophages function, thereby it may unravel part of the complexity of IL-17 in OB and enhance future therapeutic development.

Keywords: IL-17; Macrophages; Obliterative bronchiolitis; Trachea transplantation.

MeSH terms

  • Animals
  • Bronchiolitis Obliterans / immunology*
  • Cell Differentiation
  • Cytokines / genetics
  • Cytokines / metabolism
  • Disease Models, Animal
  • Interleukin-17 / genetics
  • Interleukin-17 / metabolism*
  • Macrophages / immunology*
  • Male
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism
  • Receptors, Immunologic
  • STAT3 Transcription Factor / metabolism
  • STAT5 Transcription Factor / metabolism
  • Th1 Cells / immunology
  • Trachea / surgery
  • Transplantation, Heterotopic

Substances

  • Cytokines
  • Interleukin-17
  • MRC1 protein, mouse
  • Membrane Glycoproteins
  • Receptors, Cell Surface
  • Receptors, Immunologic
  • STAT3 Transcription Factor
  • STAT5 Transcription Factor
  • Stat3 protein, mouse