Eosinophils control the resolution of inflammation and draining lymph node hypertrophy through the proresolving mediators and CXCL13 pathway in mice

FASEB J. 2014 Sep;28(9):4036-43. doi: 10.1096/fj.14-251132. Epub 2014 Jun 2.

Abstract

Resolution of inflammation is critical to restoration of tissue function after an inflammatory response. We previously demonstrated that 12/15-lipoxygenase (12/15-LOX)-expressing eosinophils contribute to this process in murine zymosan-induced peritonitis. In this study, eosinophils promoted resolution by regulating expression of macrophage CXCL13. Microarray analysis revealed that eosinophils significantly increased (∼3-fold) the expression of macrophage CXCL13 by a 12/15-LOX-dependent mechanism. CXCL13 depletion caused a resolution defect, with the reduced appearance of phagocytes carrying engulfed zymosan in the draining lymph nodes. Inflamed lymph node hypertrophy, a critical feature of the resolution process, was reduced by ∼60% in eosinophil-deficient mice, and adoptive transfer of eosinophils or administration of CXCL13 corrected this defect. Administration of the 12/15-LOX-derived mediator lipoxin A4 (LXA4) increased the expression of CXCL13 and restored the defect of lymph node hypertrophy in eosinophil-deficient mice. These results demonstrate that eosinophils control the resolution of inflammation and draining lymph node hypertrophy through proresolving lipid mediators and the CXCL13 pathway in mice.

Keywords: lipid mediator; lipoxygenase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arachidonate 12-Lipoxygenase / metabolism*
  • Arachidonate 15-Lipoxygenase / metabolism*
  • Cells, Cultured
  • Chemokine CXCL13 / metabolism*
  • Eosinophils / cytology*
  • Eosinophils / metabolism
  • Flow Cytometry
  • Hypertrophy
  • Inflammation / metabolism
  • Inflammation / pathology*
  • Lipoxins / metabolism
  • Lymph Nodes / metabolism
  • Lymph Nodes / pathology*
  • Macrophages, Peritoneal / metabolism
  • Macrophages, Peritoneal / pathology*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Microarray Analysis
  • Peritonitis / metabolism
  • Peritonitis / pathology*

Substances

  • 12-15-lipoxygenase
  • Chemokine CXCL13
  • Cxcl13 protein, mouse
  • Lipoxins
  • lipoxin A4
  • Arachidonate 12-Lipoxygenase
  • Arachidonate 15-Lipoxygenase