Accumulation of ceramide in the trachea and intestine of cystic fibrosis mice causes inflammation and cell death

Biochem Biophys Res Commun. 2010 Dec 17;403(3-4):368-74. doi: 10.1016/j.bbrc.2010.11.038. Epub 2010 Nov 13.


Cystic fibrosis is a hereditary metabolic disorder caused by mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene and characterized by severe intestinal and pulmonary symptoms, in particular intestinal obstruction, pancreatic insufficiency, chronic pulmonary inflammation, and microbial lung infections. Recent studies have demonstrated an accumulation of ceramide in the lungs of cystic fibrosis patients and in several mouse models. These findings showed that pulmonary ceramide concentrations play an important role in pulmonary inflammation and infection. In this study we investigated whether ceramide concentrations are also altered in the trachea and the intestine of cystic fibrosis mice and whether an accumulation of ceramide in these organs has functional consequences that are typical of cystic fibrosis. Our findings demonstrate a marked accumulation of ceramide in tracheal and intestinal epithelial cells of cystic fibrosis mice. When acid sphingomyelinase activity is inhibited by treating cystic fibrosis mice with amitriptyline or by genetic heterozygosity of acid sphingomyelinase in cystic fibrosis mice, ceramide concentrations in the trachea and the intestine are normalized. Moreover, increased rates of cell death and increased cytokine concentrations in the trachea, the intestine, or both were normalized by the inhibition of acid sphingomyelinase activity and the concomitant normalization of ceramide concentrations. These findings suggest that ceramide plays a crucial role in inflammation and increased rates of cell death in several organs of cystic fibrosis mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Death
  • Ceramides / metabolism*
  • Cystic Fibrosis / metabolism*
  • Cystic Fibrosis / pathology
  • Cytokines / metabolism
  • Inflammation / metabolism
  • Inflammation / pathology
  • Intestinal Mucosa / metabolism*
  • Intestines / pathology
  • Mice
  • Mice, Congenic
  • Mice, Inbred CFTR
  • Trachea / metabolism*
  • Trachea / pathology


  • Ceramides
  • Cytokines