Repeated intrauterine exposures to inflammatory stimuli attenuated transforming growth factor-β signaling in the ovine fetal lung

Neonatology. 2013;104(1):49-55. doi: 10.1159/000350548. Epub 2013 May 24.

Abstract

Background: Bronchopulmonary dysplasia (BPD) is one of the most common complications after preterm birth and is associated with intrauterine exposure to bacteria. Transforming growth factor-β (TGFβ) is implicated in the development of BPD.

Objectives: We hypothesized that different and/or multiple bacterial signals could elicit divergent TGFβ signaling responses in the developing lung.

Methods: Time-mated pregnant Merino ewes received an intra-amniotic injection of lipopolysaccharide (LPS) and/or Ureaplasma parvum serovar 3 (UP) at 117 days' and/or 121/122 days' gestational age (GA). Controls received an equivalent injection of saline and or media. Lambs were euthanized at 124 days' GA (term = 150 days' GA). TGFβ1, TGFβ2, TGFβ3, TGFβ receptor (R)1 and TGFβR2 protein levels, Smad2 phosphorylation and elastin deposition were evaluated in lung tissue.

Results: Total TGFβ1 and TGFβ2 decreased by 24 and 51% after combined UP+LPS exposure, whereas total TGFβ1 increased by 31% after 7 days' LPS exposure but not after double exposures. Alveolar expression of TGFβR2 decreased 75% after UP, but remained unaltered after double exposures. Decreased focal elastin deposition after single LPS exposure was prevented by double exposures.

Conclusions: TGFβ signaling components and elastin responded differently to intrauterine LPS and UP exposure. Multiple bacterial exposures attenuated TGFβ signaling and normalized elastin deposition.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amnion / drug effects
  • Animals
  • Chorioamnionitis
  • Disease Models, Animal
  • Elastin / analysis
  • Female
  • Gestational Age
  • Inflammation / physiopathology*
  • Lipopolysaccharides / administration & dosage
  • Lung / chemistry
  • Lung / embryology*
  • Phosphorylation
  • Pregnancy
  • Pregnancy Complications / physiopathology*
  • Receptors, Transforming Growth Factor beta / analysis
  • Sheep / embryology*
  • Signal Transduction*
  • Smad2 Protein / metabolism
  • Transforming Growth Factor beta / physiology*
  • Transforming Growth Factor beta1 / analysis
  • Transforming Growth Factor beta2 / analysis
  • Transforming Growth Factor beta3 / analysis
  • Ureaplasma

Substances

  • Lipopolysaccharides
  • Receptors, Transforming Growth Factor beta
  • Smad2 Protein
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • Transforming Growth Factor beta2
  • Transforming Growth Factor beta3
  • Elastin