bioRxivPhysiology
Molecular programming in utero modulates hepatic lipid metabolism and adult metabolic risk in obese mother offspring in a sex-specific manner
C. Savva, L. A. Helguero, M. Gonzalez-Granillo, T. Melo, D. Couto, B. Angelin, M. R. Domingues, X. Li, C. Kutter, M. Korach-Andre
Abstract
Male and female offspring of obese mothers are known to differ significantly in their metabolic adaptation and later development of complications. We investigated the sex-dependent responses in obese offspring of mice with maternal obesity, focusing on changes in liver glucose and lipid metabolism. Maternal obesity prior to and during gestation led to hepatic insulin resistance and inflammation in male offspring, while female offspring were protected. These sex differences were explained by more efficient transcriptional and posttranscriptional reprogramming of metabolic pathways to prevent the damaging effects of maternal obesity in females compared to males. These differences were sustained later in life, resulting in a better metabolic balance in female offspring. In conclusion, sex and maternal obesity drive transcriptional and posttranscriptional regulation of major metabolic processes in offspring liver differently, explaining the sexual dimorphism in obesity-associated metabolic risk.
- organism: mouse
- assay: bulk RNA-seq
- research focus: metabolism & bioenergetics
- research focus: cell type annotation
- research focus: differential expression
- approach: experimental assay
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