Abstract

Maternal nutrient restriction impairs placental growth and development, but available evidence suggests that adaptive mechanisms exist, in a subset of nutrient restricted (NR) ewes, that support normal fetal growth and do not result in intrauterine growth restriction (IUGR). This study utilized Affymetrix GeneChip Bovine and Ovine Genome 1.0 ST Arrays to identify novel placental genes associated with differential fetal growth rates within NR ewes. Singleton pregnancies were generated by embryo transfer and, beginning on Day 35 of pregnancy, ewes received either a 100% National Research Council (NRC) (control-fed group; n = 7) or 50% NRC (NR group; n = 24) diet until necropsy on Day 125. Fetuses from NR ewes were separated into NR non-IUGR (n = 6) and NR IUGR (n = 6) groups based on Day 125 fetal weight for microarray analysis. Of the 103 differentially expressed genes identified, 15 were upregulated and 88 were downregulated in NR non-IUGR compared to IUGR placentomes. Bioinformatics analysis revealed that upregulated gene clusters in NR non-IUGR placentomes associated with cell membranes, receptors, and signaling. Downregulated gene clusters associated with immune response, nutrient transport, and metabolism. Results illustrate that placentomal gene expression in late gestation is indicative of an altered placental immune response, which is associated with enhanced fetal growth, in a subpopulation of NR ewes.

Highlights

  • Maternal nutrient restriction during pregnancy impairs placental and fetal growth in humans and livestock species, often resulting in intrauterine growth restriction (IUGR) [1,2,3]

  • Results illustrate that placentomal gene expression in late gestation is indicative of an altered placental immune response, which is associated with enhanced fetal growth, in a subpopulation of nutrient restricted (NR) ewes

  • The specific nutrient transporters that were upregulated in the non-IUGR compared to IUGR placentomes from NR ewes previously, were not detected in this microarray [15]

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Summary

Introduction

Maternal nutrient restriction during pregnancy impairs placental and fetal growth in humans and livestock species, often resulting in intrauterine growth restriction (IUGR) [1,2,3]. In response to reduced nutrient delivery from the dam, the fetus undergoes a number of adaptations to reset critical metabolic and physiologic functions that will allow for enhanced survival in postnatal life [6,8]. The mechanisms regulating this adaptation in fetal growth, development, and programming are not fully understood

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