Secreted hCLCA1 is a signaling molecule that activates airway macrophages

PLoS One. 2013 Dec 12;8(12):e83130. doi: 10.1371/journal.pone.0083130. eCollection 2013.

Abstract

The CLCA gene family produces both secreted and membrane-associated proteins that modulate ion-channel function, drive mucus production and have a poorly understood pleiotropic effect on airway inflammation. The primary up-regulated human CLCA ortholog in airway inflammation is hCLCA1. Here we show that this protein can activate airway macrophages, inducing them to express cytokines and to undertake a pivotal role in airway inflammation. In a U-937 airway macrophage-monocyte cell line, conditioned media from HEK 293 cells heterologously expressing hCLCA1 (with or without fetal bovine serum) increased the levels of pro-inflammatory cytokines (IL-1β, IL-6, TNF-α and IL-8). This effect was independent of the metalloprotease domain of hCLCA1. Primary porcine alveolar macrophages were similarly activated, demonstrating the effect was not cell line dependent. Similarly, immuno-purified hCLCA1 at physiologically relevant concentration of ~100 pg/mL was able to activate macrophages and induce pro-inflammatory response. This cytokine response increased with higher concentration of immuno-purified hCLCA1. These findings demonstrate the ability of hCLCA1 to function as a signaling molecule and activate macrophages, central regulators of airway inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Chloride Channels / immunology
  • Chloride Channels / metabolism*
  • Cytokines / biosynthesis
  • Cytokines / immunology
  • HEK293 Cells
  • Humans
  • Inflammation / immunology
  • Inflammation / metabolism
  • Inflammation / pathology
  • Macrophage Activation*
  • Macrophages, Alveolar / immunology
  • Macrophages, Alveolar / metabolism*
  • Macrophages, Alveolar / pathology
  • Protein Structure, Tertiary
  • Signal Transduction*
  • Swine
  • U937 Cells

Substances

  • CLCA1 protein, human
  • Chloride Channels
  • Cytokines

Grants and funding

The work was supported by a Natural Sciences and Engineering Research Council of Canada Discovery Grant 371364-2010 (MEL), a Saskatchewan Health Research Foundation New Investigator Grant (MEL), the Ryan Dubé Equine Health Research Fund and the Canada Foundation for Innovation (MEL). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.