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Published on: April 14, 2023
Molecular and morphological changes in placenta and embryo development associated with the inhibition of polyamine
Carlos López-García1, Andrés Joaquín López-Contreras, Asunción Cremades
1Department of Biochemistry and Molecular Biology B and Immunology, Faculty of Medicine, University of Murcia, Campus de Espinardo, 30100 Murcia, Spain.
Abstract:
Polyamines play an essential role in murine development, as demonstrated by both gene ablation in ornithine decarboxylase (ODC)-deficient embryos and pharmacological treatments of pregnant mice. However, the molecular and cellular mechanisms by which ODC inhibition affects embryonic development during critical periods of pregnancy are mostly unknown. Our present results demonstrate that the contragestational effect of alpha-difluoromethylornithine (DFMO), a suicide inhibitor of ODC, when given at d 7-9 of pregnancy, is associated with embryo growth arrest and marked alterations in the development of yolk sac and placenta. Blood island formation as well as the transcript levels of embryonary globins alpha-like x chain and beta-like y-chain was markedly decreased in the yolk sac. At the placental level, abnormal chorioallantoic attachment, absence of the spongiotrophoblast layer and a deficient development of the labyrinthine zone were evident. Real-time RT-PCR analysis showed that transcript levels of the steroidogenic genes steroidogenic acute regulatory protein, 3beta-hydroxysteroid dehydrogenase VI, and 17alpha-hydroxylase were markedly decreased by DFMO treatment in the developing placenta at d 9 and 10 of pregnancy. Plasma values of progesterone and androstenedione were also decreased by DFMO treatment. Transcriptomic analysis also detected changes in the expression of several genes involved in placentation and the differentiation of trophoblastic lineages. In conclusion, our results indicate that ODC inhibition at d 8 of pregnancy is related to alterations in yolk sac formation and trophoblast differentiation, affecting processes such as vasculogenesis and steroidogenesis.
Insights
Alpha-difluoromethylornithine (DFMO) inhibits ornithine decarboxylase (ODC), hindering embryonic development. DFMO treatment during early pregnancy causes embryo growth arrest and placental defects, impacting yolk sac and placenta formation.
Area of Science:
- Developmental biology
- Reproductive biology
- Biochemistry
Background:
- Polyamines are crucial for murine embryonic development.
- The precise mechanisms of ornithine decarboxylase (ODC) inhibition during pregnancy are not fully understood.
Purpose of the Study:
- To investigate the molecular and cellular effects of ODC inhibition on embryonic development during critical pregnancy periods.
- To elucidate the contragestational mechanisms of alpha-difluoromethylornithine (DFMO).
Main Methods:
- Pharmacological inhibition of ODC using alpha-difluoromethylornithine (DFMO) in pregnant mice.
- Analysis of embryonic and placental development, including yolk sac and chorioallantoic attachment.
- Real-time RT-PCR to quantify transcript levels of key developmental and steroidogenic genes.
- Transcriptomic analysis to identify affected gene expression pathways.
Main Results:
- DFMO treatment at days 7-9 of pregnancy led to embryo growth arrest.
- Significant alterations were observed in yolk sac development, including reduced blood island formation and embryonic globin expression.
- Placental abnormalities included defective chorioallantoic attachment, absent spongiotrophoblast, and impaired labyrinthine zone development.
- DFMO decreased transcript levels of steroidogenic genes (StAR, 3β-HSD, P450c17) and plasma levels of progesterone and androstenedione.
- Gene expression changes indicated impacts on placentation and trophoblast differentiation, affecting vasculogenesis and steroidogenesis.
Conclusions:
- ODC inhibition by DFMO during early pregnancy disrupts embryonic development.
- DFMO affects yolk sac formation and placental development, including trophoblast differentiation, vasculogenesis, and steroidogenesis.

