A CCL24-dependent pathway augments eosinophilic airway inflammation in house dust mite-challenged Cd163(-/-) mice

Mucosal Immunol. 2016 May;9(3):702-17. doi: 10.1038/mi.2015.94. Epub 2015 Sep 16.

Abstract

CD163 is a macrophage scavenger receptor with anti-inflammatory and pro-inflammatory functions. Here, we report that alveolar macrophages (AMΦs) from asthmatic subjects had reduced cell-surface expression of CD163, which suggested that CD163 might modulate the pathogenesis of asthma. Consistent with this, house dust mite (HDM)-challenged Cd163(-/-) mice displayed increases in airway eosinophils and mucous cell metaplasia (MCM). The increased airway eosinophils and MCM in HDM-challenged Cd163(-/-) mice were mediated by augmented CCL24 production and could be reversed by administration of a neutralizing anti-CCL24 antibody. A proteomic analysis identified the calcium-dependent binding of CD163 to Dermatophagoides pteronyssinus peptidase 1 (Der p1). Der p1-challenged Cd163(-/-) mice had the same phenotype as HDM-challenged Cd163(-/-) mice with increases in airway eosinophils, MCM and CCL24 production, while Der p1 induced CCL24 secretion by bone marrow-derived macrophages (BMMΦs) from Cd163(-/-) mice, but not BMMΦs from wild-type (WT) mice. Finally, airway eosinophils and bronchoalveolar lavage fluid CCL24 levels were increased in Der p1-challenged WT mice that received adoptively transferred AMΦ's from Cd163(-/-) mice. Thus, we have identified CD163 as a macrophage receptor that binds Der p1. Furthermore, we have shown that HDM-challenged Cd163(-/-) mice have increased eosinophilic airway inflammation and MCM that are mediated by a CCL24-dependent mechanism.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Antibodies, Neutralizing / administration & dosage
  • Antigens, CD / genetics
  • Antigens, CD / metabolism*
  • Antigens, Dermatophagoides / immunology
  • Antigens, Dermatophagoides / metabolism
  • Antigens, Differentiation, Myelomonocytic / genetics
  • Antigens, Differentiation, Myelomonocytic / metabolism*
  • Arthropod Proteins / immunology
  • Arthropod Proteins / metabolism
  • Asthma / immunology*
  • Cell Movement
  • Cells, Cultured
  • Chemokine CCL24 / immunology
  • Chemokine CCL24 / metabolism*
  • Cysteine Endopeptidases / immunology
  • Cysteine Endopeptidases / metabolism
  • Eosinophils / immunology*
  • Humans
  • Macrophages, Alveolar / immunology*
  • Macrophages, Alveolar / transplantation
  • Metaplasia
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Pyroglyphidae
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism*
  • Respiratory Mucosa / pathology*

Substances

  • Antibodies, Neutralizing
  • Antigens, CD
  • Antigens, Dermatophagoides
  • Antigens, Differentiation, Myelomonocytic
  • Arthropod Proteins
  • CD163 antigen
  • Chemokine CCL24
  • Receptors, Cell Surface
  • Cysteine Endopeptidases
  • Dermatophagoides pteronyssinus antigen p 1