Morphological and Functional Alterations of Alveolar Macrophages in a Murine Model of Chronic Inflammatory Lung Disease

Lung. 2015 Dec;193(6):947-53. doi: 10.1007/s00408-015-9797-4. Epub 2015 Aug 30.

Abstract

Purpose: Chronic lung inflammation commonly induces a multitude of structural and functional adaptations within the lung tissue and airspaces. Yet the impact of a persistent inflammatory environment on alveolar macrophages is still incompletely understood. Here, we examined morphology and function of alveolar macrophages in a transgenic mouse model of chronic lung disease.

Methods: Imaging flow cytometry, flow cytometry, and microscopic evaluation of alveolar macrophages isolated from healthy and inflamed lungs were performed. Gene expression of polarization markers was compared by quantitative real-time RT-PCR. The pro-inflammatory immune response of alveolar macrophages toward bacterial ligands was assessed in in vivo clodronate-liposome depletion studies.

Results: Chronic lung inflammation is associated with a substantially altered, activated alveolar macrophage morphology, and blunted TNF-α response by these cells following stimulation with ligands derived from the respiratory pathogen Streptococcus pneumoniae.

Conclusions: These results demonstrate pleiotropic effects of pulmonary inflammation on alveolar macrophage phenotype and function and suggest a functional impairment of these cells during infection with airborne pathogens.

Keywords: Alveolar macrophage; Chronic lung disease; Infection; Inflammation; Macrophage polarization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoimmune Diseases / immunology*
  • Chronic Disease
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Inflammation / immunology*
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / immunology*
  • Lung Diseases / immunology*
  • Macrophages, Alveolar / immunology*
  • Macrophages, Alveolar / metabolism
  • Mice
  • Mice, Transgenic
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Scavenger Receptors, Class A / genetics
  • Scavenger Receptors, Class A / immunology*
  • Streptococcal Infections / immunology*
  • Streptococcus pneumoniae / immunology
  • Tumor Necrosis Factor-alpha / immunology*

Substances

  • Intercellular Signaling Peptides and Proteins
  • Msr1 protein, mouse
  • Retnla protein, mouse
  • Scavenger Receptors, Class A
  • Tumor Necrosis Factor-alpha