Up-regulation of connective tissue growth factor in hyperoxia-induced lung fibrosis

Pediatr Res. 2007 Aug;62(2):128-33. doi: 10.1203/PDR.0b013e3180987202.

Abstract

Pulmonary oxygen toxicity plays an important role in the lung injury process that leads to the development of bronchopulmonary dysplasia. Connective tissue growth factor (CTGF) is a fibroblast mitogen and promoter of collagen deposition. We investigated the effects of postnatal hyperoxia on lung collagen and CTGF expression in rats. Rat pups were exposed to 7 d of >95% O2 and a further 3 wk of 60% O2. CTGF mRNA and protein expression increased after hyperoxia treatment, and the values were significantly higher in hyperoxia-exposed rats on postnatal d 7 and 14. Lung collagen levels increased as rats aged, and the values were comparable between room air-exposed and hyperoxia-exposed rats on postnatal d 7 and 14 and were significantly higher in hyperoxia-exposed rats on postnatal d 21 and 28. Increases in CTGF mRNA and protein expressions preceded the onset of increased lung collagen. These data demonstrate that CTGF is up-regulated at time points preceding the fibrotic phase of the lung injury adding credence to the hypothesis that CTGF seems to be involved in the pathogenesis of hyperoxia-induced lung fibrosis and an anti-CTGF strategy might attenuate hyperoxia-induced lung fibrosis.

MeSH terms

  • Animals
  • Animals, Newborn
  • Apoptosis
  • Blotting, Western
  • Body Weight
  • Collagen / genetics
  • Collagen / metabolism*
  • Connective Tissue Growth Factor
  • Disease Models, Animal
  • Hyperoxia / chemically induced
  • Hyperoxia / complications*
  • Hyperoxia / genetics
  • Hyperoxia / metabolism
  • Hyperoxia / pathology
  • Immediate-Early Proteins / genetics
  • Immediate-Early Proteins / metabolism*
  • Immunohistochemistry
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Lung / metabolism*
  • Lung / pathology
  • Organ Size
  • Oxygen
  • Pulmonary Fibrosis / etiology
  • Pulmonary Fibrosis / genetics
  • Pulmonary Fibrosis / metabolism*
  • Pulmonary Fibrosis / pathology
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors
  • Up-Regulation

Substances

  • CCN2 protein, rat
  • Immediate-Early Proteins
  • Intercellular Signaling Peptides and Proteins
  • RNA, Messenger
  • Connective Tissue Growth Factor
  • Collagen
  • Oxygen