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Am J Physiol Lung Cell Mol Physiol 287: L1207-L1214, 2004. First published August 6, 2004; doi:10.1152/ajplung.00375.2003
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Regulation of alveolar epithelial cell phenotypes in fetal sheep: roles of cortisol and lung expansion

Sharon J. Flecknoe, Rochelle E. Boland, Megan J. Wallace, Richard Harding, and Stuart B. Hooper

Department of Physiology, Monash University, Victoria 3800, Australia

Submitted 31 October 2003 ; accepted in final form 28 July 2004

Our aim was to determine whether cortisol's effect on alveolar epithelial cell (AEC) phenotypes in the fetus is mediated via a sustained alteration in lung expansion. Chronically catheterized fetal sheep were exposed to 1) saline infusion, 2) cortisol infusion (122–131 days' gestation, 1.5–4.0 mg/day), 3) saline infusion plus reduced lung expansion, or 4) cortisol infusion plus reduced lung expansion. The proportions of type I and II AECs were determined by electron microscopy, and surfactant protein (SP)-A, -B, and -C mRNA levels were determined by Northern blot analysis. Cortisol infusions significantly increased type II AEC proportions (to 38.2 ± 2.2%), compared with saline-infused fetuses (23.8 ± 2.4%), and reduced type I AEC proportions (to 59.0 ± 2.2%), compared with saline-infused fetuses (70.4 ± 2.4%). Reduced lung expansion also increased type II AEC proportions (to 52.9 ± 3.5%) and decreased type I AEC proportions (to 34.2 ± 3.7%), compared with control, saline-infused fetuses. The infusion of cortisol into fetuses exposed to reduced lung expansion tended to further increase type II (to 60.3 ± 2.1%, P = 0.066) and reduce type I AEC (to 26.6 ± 2.3%, P = 0.07) proportions. SP-A, -B, and -C mRNA levels changed in parallel with the changes in type II AEC proportions. These results indicate that cortisol alters the proportion of type I and type II AECs via a mechanism unrelated to the degree of fetal lung expansion. However, reductions in fetal lung expansion appear to have a greater impact on the proportion of AECs than cortisol.

lung liquid; surfactant proteins; fetus



Address for reprint requests and other correspondence: S. J. Flecknoe, Dept. of Physiology, Monash Univ., Victoria, 3800, Australia (E-mail: sharon.flecknoe{at}med.monash.edu.au)




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