Gene expression of profibrotic mediators in bronchiolitis obliterans syndrome after lung transplantation

Scand Cardiovasc J. 1998;32(2):97-103. doi: 10.1080/14017439850140247.

Abstract

Bronchiolitis obliterans syndrome (BOS) develops in one-third of lung transplant recipients. A fibroproliferative process involving mesenchymal cells is observed histopathologically. In order further to evaluate the pathomechanisms of BOS, the gene expression of platelet-derived growth factor (PDGF)-B and transforming growth factor (TGF)-beta 1 in bronchoalveolar lavage (BAL) cells of six lung transplant recipients and appropriate controls was studied. Equal amounts of total RNA were submitted to semiquantitative reverse transcription/polymerase chain reaction (RT-PCR), amplifying actin, PDGF-B and TGF-beta 1 using established protocols and primer sets. The signal/actin ratio was calculated based on laser densitometry measurements. TGF-beta 1 transcripts were detected in all samples, and a slight increase in BOS patients was observed. PDGF-B mRNA was increased in BAL samples from BOS patients compared to unaffected recipients and controls. Plotting the FEV1 in percent of vital capacity and the PDGF expression in BOS patients revealed an increased PDGF signal preceding lung function deterioration. The data were consistent with the hypothesis based mainly on in vitro findings that PDGF and TGF-beta contribute to the development of BOS.

Publication types

  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial

MeSH terms

  • Adult
  • Bronchiolitis Obliterans / blood
  • Bronchiolitis Obliterans / diagnosis
  • Bronchiolitis Obliterans / genetics*
  • Bronchoalveolar Lavage Fluid / cytology*
  • Bronchoscopy
  • Cytomegalovirus Infections / etiology
  • Female
  • Gene Expression Regulation
  • Graft vs Host Reaction / genetics
  • Humans
  • Leukocyte Count
  • Lung Transplantation / adverse effects*
  • Male
  • Middle Aged
  • Platelet-Derived Growth Factor / biosynthesis
  • Platelet-Derived Growth Factor / genetics*
  • Polymerase Chain Reaction / methods
  • Pulmonary Fibrosis / etiology
  • RNA, Messenger / analysis*
  • Respiratory Distress Syndrome / etiology
  • Respiratory Function Tests
  • Transcription, Genetic
  • Transforming Growth Factor beta / biosynthesis
  • Transforming Growth Factor beta / genetics*

Substances

  • Platelet-Derived Growth Factor
  • RNA, Messenger
  • Transforming Growth Factor beta