Proteomic identification of macrophage migration-inhibitory factor upon exposure to TiO2 particles

Mol Cell Proteomics. 2007 Jan;6(1):56-63. doi: 10.1074/mcp.M600234-MCP200. Epub 2006 Oct 6.

Abstract

Inhalation of particulate matter aggravates respiratory symptoms in patients with chronic airway diseases, but the mechanisms underlying this response remain poorly understood. We used a proteomics approach to examine this phenomenon. Treatment of epithelial cells with BSA-coated titanium dioxide (TiO(2)) particles altered 20 protein spots on the two-dimensional gel, and these were then analyzed by nano-LC-MS/MS. These proteins included defense-related, cell-activating, and cytoskeletal proteins implicated in the response to oxidative stress. The proteins were classified into four groups according to the time course of their expression patterns. For validation, RT-PCR was performed on extracts of in vitro TiO(2)-treated cells, and lung issues from TiO(2)-treated rats were analyzed by immunohistochemical staining and enzyme immunoassay. TiO(2) treatment was found to increase the amount of mRNA for macrophage migration-inhibitory factor (MIF). MIF was expressed primarily in epithelium and was elevated in lung tissues and bronchoalveolar lavage fluids of TiO(2)-treated rats as compared with sham-treated rats. Carbon black and diesel exhaust particles also induced expression of MIF protein in the epithelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Bronchoalveolar Lavage Fluid / chemistry
  • Chloride Channels / analysis
  • Chloride Channels / chemistry
  • Chloride Channels / genetics
  • Cluster Analysis
  • Cytoplasm / drug effects
  • Electrophoresis, Gel, Two-Dimensional
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Gene Expression Regulation / drug effects
  • Humans
  • Lung / cytology
  • Lung / drug effects
  • Lung / pathology
  • Macrophage Migration-Inhibitory Factors / analysis*
  • Macrophage Migration-Inhibitory Factors / biosynthesis
  • Macrophage Migration-Inhibitory Factors / chemistry
  • Macrophage Migration-Inhibitory Factors / genetics
  • Male
  • Molecular Sequence Data
  • Particulate Matter / toxicity*
  • Proteomics / methods*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Titanium / toxicity*
  • Transaldolase / analysis
  • Transaldolase / chemistry
  • Transaldolase / genetics

Substances

  • Chloride Channels
  • Clic1 protein, mouse
  • Macrophage Migration-Inhibitory Factors
  • Particulate Matter
  • RNA, Messenger
  • titanium dioxide
  • Titanium
  • Transaldolase