Laser-assisted microdissection and real-time PCR detect anti-inflammatory effect of perfluorocarbon

Am J Physiol Lung Cell Mol Physiol. 2003 Jul;285(1):L55-62. doi: 10.1152/ajplung.00198.2002. Epub 2003 Feb 21.

Abstract

The aim of this study was to identify cell types involved in the anti-inflammatory effect of ventilation with perfluorocarbon in vivo. Fifteen anesthetized, surfactant-depleted piglets received either aerosolized perfluorocarbon (Aerosol-PFC), partial liquid ventilation (rLV) at functional residual capacity (FRC) volume (FRC-PLV), or intermittent mandatory ventilation (control). After laser-assisted microdissection of different lung cell types, mRNA expression of IL-8 and ICAM-1 was determined using TaqMan real-time PCR normalized to hypoxanthine phosphoribosyltransferase (HPRT). IL-8 mRNA expression (means +/- SE; control vs. Aerosol-PFC) was 356 +/- 142 copies IL-8 mRNA/copy HPRT mRNA vs. 3.5 +/- 1.8 in alveolar macrophages (P <0.01); 208 +/- 108 vs. 2.7 +/- 0.8 in bronchiolar epithelial cells (P <0.05); 26 +/- 11 vs. 0.7 +/- 0.2 in alveolar septum cells (P <0.01); 2.8 +/- 1.0 vs. 0.8 +/- 0.4 in bronchiolar smooth muscle cells (P <0.05); and 1.1 +/- 0.4 vs. 0.2 +/- 0.05 in vascular smooth muscle cells (P <0.05). With FRC-PLV, IL-8/HPRT mRNA expression was significantly lower in macrophages, bronchiolar epithelial, and vascular smooth muscle cells. ICAM-1 mRNA expression in vascular endothelial cells remained unchanged. Predominantly, alveolar macrophages and bronchiolar epithelial cells were involved in the inflammatory pulmonary process. The anti-inflammatory effect of Aerosol-PFC was most pronounced.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dissection / methods*
  • Fluorocarbons / pharmacology*
  • Hypoxanthine Phosphoribosyltransferase / genetics
  • Immunohistochemistry
  • Intercellular Adhesion Molecule-1 / genetics
  • Interleukin-8 / genetics*
  • Interleukin-8 / immunology
  • Lasers
  • Macrophages, Alveolar / drug effects
  • Macrophages, Alveolar / immunology
  • Miniaturization
  • Muscle, Smooth, Vascular / cytology
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / immunology
  • Oxygen / metabolism
  • Pneumonia / drug therapy*
  • Pneumonia / immunology
  • Polymerase Chain Reaction / methods
  • Pulmonary Alveoli / cytology
  • Pulmonary Alveoli / drug effects*
  • Pulmonary Alveoli / immunology
  • Pulmonary Surfactants / metabolism
  • RNA, Messenger / analysis
  • Respiratory Mucosa / cytology
  • Respiratory Mucosa / drug effects
  • Respiratory Mucosa / immunology
  • Swine

Substances

  • Fluorocarbons
  • Interleukin-8
  • Pulmonary Surfactants
  • RNA, Messenger
  • Intercellular Adhesion Molecule-1
  • Hypoxanthine Phosphoribosyltransferase
  • Oxygen