4.2 Article

Maternal Undernutrition Induces the Expression of Hypoxia-Related Genes in the Fetal Brain

Journal

TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE
Volume 226, Issue 1, Pages 37-44

Publisher

TOHOKU UNIV MEDICAL PRESS
DOI: 10.1620/tjem.226.37

Keywords

fetal brain; hypoxia-inducible factor 1 alpha; hypoxic responses; mammalian target of rapamycin; maternal undernutrition

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Maternal undernutrition during pregnancy is a risk factor for cerebrovascular and cardiovascular diseases in adulthood. Hypoxia-inducible factor 1 alpha (HIF1 alpha) plays an essential role in cellular hypoxic responses, and its increased expression is associated with cerebrovascular and cardiovascular diseases. However, it is not known whether maternal undernutrition influences HIF1 alpha expression in the fetal brain. We therefore analyzed the expression levels of HIFI a and its downstream genes in the fetal brain (day 17.5 of gestation, 1-2 days before birth). Maternal undernutrition did not noticeably affect the fetal body and brain weights. Both HIF1 alpha mRNA and protein levels were increased in the brain under maternal undernutrition, despite the absence of hypoxia, as judged by the staining profile with hypoxyprobe-1 that identifies hypoxic cells. Importantly, maternal undernutrition caused the accumulation of HIF1 alpha protein in oligodendrocyte precursor cells at the subventricular zone, a site of neurogenesis in the fetal brain. Maternal undernutrition also increased the mRNA level of mammalian target of rapamycin (mTOR), which could increase the level of HIF1 alpha protein under normoxia. Furthermore, microarray analysis revealed that expression levels of mRNAs for 10 HIF1 alpha downstream targets, including enolase 1 and hexokinase 1, were increased in the fetal brain under maternal undernutrition. Thus, the biochemical consequence of maternal undernutrition is similar to that of mild hypoxia. In conclusion, maternal undernutrition induces the expression of HIF1 alpha in oligodendrocyte precursor cells at the subventricular zone, and it also induces the expression of hypoxia-related genes in the fetal brain probably via activation of the mTOR pathway.

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