Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/96871
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Type: Journal article
Title: Increased lung prolyl hydroxylase and decreased glucocorticoid receptor are related to decreased surfactant protein in the growth-restricted sheep fetus
Author: Orgeig, S.
McGillick, E.
Botting, K.
Zhang, S.
McMillen, I.
Morrison, J.
Citation: American Journal of Physiology-Lung Cellular and Molecular Physiology, 2015; 309(1):L84-L97
Publisher: American Physiological Society
Issue Date: 2015
ISSN: 1040-0605
1522-1504
Statement of
Responsibility: 
Sandra Orgeig, Erin V. McGillick, Kimberley J. Botting, Song Zhang, I. Caroline McMillen, and Janna L. Morrison
Abstract: Experimental placental restriction (PR) by carunclectomy in fetal sheep results in intrauterine growth restriction (IUGR), chronic hypoxemia, increased plasma cortisol, and decreased lung surfactant protein (SP) expression. The mechanisms responsible for decreased SP expression are unknown but may involve decreased glucocorticoid (GC) action or changes in hypoxia signaling. Endometrial caruncles were removed from nonpregnant ewes to induce PR. Lungs were collected from control and PR fetuses at 130-135 (n = 19) and 139-145 (n = 28) days of gestation. qRT-PCR and Western blotting were used to quantify lung mRNA and protein expression, respectively, of molecular regulators and downstream targets of the GC and hypoxia-signaling pathways. We confirmed a decrease in SP-A, -B, and -C, but not SP-D, mRNA expression in PR fetuses at both ages. There was a net downregulation of GC signaling with a reduction in GC receptor (GR)-α and -β protein expression and a decrease in the cofactor, GATA-6. GC-responsive genes including transforming growth factor-β1, IL-1β, and β2-adrenergic receptor were not stimulated. Prolyl hydroxylase domain (PHD)2 mRNA and protein and PHD3 mRNA expression increased with a concomitant increase in hypoxia-inducible factor-1α (HIF-1α) and HIF-1β mRNA expression. There was an increase in mRNA expression of several, but not all, hypoxia-responsive genes. Hence, both GC and hypoxia signaling may contribute to reduced SP expression. Although acute hypoxia normally inactivates PHDs, chronic hypoxemia in the PR fetus increased PHD abundance, which normally prevents HIF signaling. This may represent a mechanism by which chronic hypoxemia contributes to the decrease in SP production in the IUGR fetal lung.
Keywords: chronic hypoxia; prolyl hydroxylase; surfactant; fetus
Description: Published 1 July 2015
Rights: Copyright © 2015 the American Physiological Society
RMID: 0030035067
DOI: 10.1152/ajplung.00275.2014
Appears in Collections:Medicine publications

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