4.6 Article

Maternal Iron Deficiency Modulates Placental Transcriptome and Proteome in Mid-Gestation of Mouse Pregnancy

Journal

JOURNAL OF NUTRITION
Volume 151, Issue 5, Pages 1073-1083

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1093/jn/nxab005

Keywords

iron deficiency; placenta; gene expression; proteomics; iron metabolism

Funding

  1. National Heart, Lung, and Blood Institute [5T32HL110852]
  2. NIH/NIGMS (National Institute of General Medical Sciences) [R01 GM132129]
  3. Children's Hospital Pathology Foundation, Inc.
  4. Harvard Catalyst, The Harvard Clinical and Translational Science Center (National Center for Advancing Translational Sciences, National Institutes of Health Award) [UL 1TR002541]
  5. Harvard University
  6. NIH Eunice Kennedy Shriver National Institute of Child Health and Human Development [U54HD090255]

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Maternal iron deficiency has limited impact on placental gene expression in mice during mid-gestation, mainly mediated by IRE coordination of iron gene expression. Interestingly, sexually dimorphic effects of maternal iron deficiency on placental gene expression were observed, with more alterations in male mouse placentas.
Background: Maternal iron deficiency (ID) is associated with poor pregnancy and fetal outcomes. The effect is thought to be mediated by the placenta but there is no comprehensive assessment of placental responses to maternal ID. Additionally, whether the influence of maternal ID on the placenta differs by fetal sex is unknown. Objectives: To identify gene and protein signatures of ID mouse placentas at mid-gestation. A secondary objective was to profile the expression of iron genes in mouse placentas across gestation. Methods: We used a real-time PCR-based array to determine the mRNA expression of all known iron genes in mouse placentas at embryonic day (E) 12.5, E14.5, E16.5, and E19.5 (n = 3 placentas/time point). To determine the effect of maternal ID, we performed RNA sequencing and proteomics in male and female placentas from ID and iron-adequate mice at E12.5 (n = 8 dams/diet). Results: In female placentas, 6 genes, including transferrin receptor (Tfrc) and solute carrier family 11 member 2, were significantly changed by maternal ID. An additional 154 genes were altered in male ID placentas. A proteomic analysis quantified 7662 proteins in the placenta. Proteins translated from iron-responsive element (IRE)-containing mRNA were altered in abundance; ferritin and ferroportin 1 decreased, while TFRC increased in ID placentas. Less than 4% of the significantly altered genes in ID placentas occurred both at the transcriptional and translational levels. Conclusions: Our data demonstrate that the impact of maternal ID on placental gene expression in mice is limited in scope and magnitude at mid-gestation. We provide strong evidence for IRE-based transcriptional and translational coordination of iron gene expression in the mouse placenta. Finally, we discover sexually dimorphic effects of maternal ID on placental gene expression, with more genes and pathways altered inmale comparedwith femalemouse placentas.

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