Hyperoxia inhibits fetal rat lung fibroblast proliferation and expression of procollagens

Naveed Hussain, Fengying Wu, Constance Christian, Mitchell J. Kresch

Research output: Contribution to journalArticle

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Abstract

The direct effects of hyperoxia on collagen production by fetal lung fibroblasts are unknown and would be important to the understanding of the molecular mechanisms involved in bronchopulmonary dysplasia in premature infants. We studied the effect of hyperoxia on 1) proliferation, 2) mRNA levels for type I and III procollagens, and 3) net collagen production in primary cultures of fetal rat lung fibroblasts. Fibroblasts from 19-day-old rat fetuses (term is 22 days) were obtained. Test plates were incubated in hyperoxia and controls in room air for varying time periods. Cell viability in both conditions was >97% as determined by trypan blue exclusion. Fibroblast proliferation in nonconfluent cultures was found to be significantly reduced with exposure to hyperoxia (P < 0.001). Steady-state levels of type I and III precollagen mRNAs, analyzed on Northern blots hybridized to [32p]cDNA probes, were significantly decreased in hyperoxia (P < 0.01). This effect was noted as early as 4 h of exposure to hyperoxia and persisted for 5 days. There was a significant inverse correlation between duration of exposure to O2 and steady-state levels of mRNA for α1(I)- procollagen (r = -0.904) and α1(III)-precollagen (r = -0.971). There were no significant changes in steady-state levels of β-actin mRNA. We also found a significant decrease in collagen synthesis in hyperoxia-exposed fibroblasts (P < 0.05). We conclude that hyperoxia directly effects a reduction in fetal lung fibroblast proliferation and net collagen production at a pretranslational level.

Original languageEnglish (US)
Pages (from-to)L726-L732
JournalAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
Volume273
Issue number4 17-4
StatePublished - Nov 17 1997

Fingerprint

Procollagen
Hyperoxia
Fibroblasts
Lung
Collagen
Messenger RNA
Multifetal Pregnancy Reduction
Bronchopulmonary Dysplasia
Collagen Type III
Trypan Blue
Premature Infants
Northern Blotting
Actins
Cell Survival
Fetus
Complementary DNA
Air

All Science Journal Classification (ASJC) codes

  • Physiology
  • Pulmonary and Respiratory Medicine
  • Physiology (medical)
  • Cell Biology

Cite this

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abstract = "The direct effects of hyperoxia on collagen production by fetal lung fibroblasts are unknown and would be important to the understanding of the molecular mechanisms involved in bronchopulmonary dysplasia in premature infants. We studied the effect of hyperoxia on 1) proliferation, 2) mRNA levels for type I and III procollagens, and 3) net collagen production in primary cultures of fetal rat lung fibroblasts. Fibroblasts from 19-day-old rat fetuses (term is 22 days) were obtained. Test plates were incubated in hyperoxia and controls in room air for varying time periods. Cell viability in both conditions was >97{\%} as determined by trypan blue exclusion. Fibroblast proliferation in nonconfluent cultures was found to be significantly reduced with exposure to hyperoxia (P < 0.001). Steady-state levels of type I and III precollagen mRNAs, analyzed on Northern blots hybridized to [32p]cDNA probes, were significantly decreased in hyperoxia (P < 0.01). This effect was noted as early as 4 h of exposure to hyperoxia and persisted for 5 days. There was a significant inverse correlation between duration of exposure to O2 and steady-state levels of mRNA for α1(I)- procollagen (r = -0.904) and α1(III)-precollagen (r = -0.971). There were no significant changes in steady-state levels of β-actin mRNA. We also found a significant decrease in collagen synthesis in hyperoxia-exposed fibroblasts (P < 0.05). We conclude that hyperoxia directly effects a reduction in fetal lung fibroblast proliferation and net collagen production at a pretranslational level.",
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Hyperoxia inhibits fetal rat lung fibroblast proliferation and expression of procollagens. / Hussain, Naveed; Wu, Fengying; Christian, Constance; Kresch, Mitchell J.

In: American Journal of Physiology - Lung Cellular and Molecular Physiology, Vol. 273, No. 4 17-4, 17.11.1997, p. L726-L732.

Research output: Contribution to journalArticle

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