Abrego-Guandique Diana Marisol, Galmés Sebastià, García-Rodríguez Adrián, Cannataro Roberto, Caroleo Maria Cristina, Ribot Joan, Bonet Maria Luisa, Cione Erika
Department of Health Sciences, University of Magna Graecia Catanzaro, 88100 Catanzaro, Italy.
Laboratory of Molecular Biology, Nutrition, and Biotechnology (LBNB), Nutrigenomics, Biomarkers and Risk Evaluation (NuBE) Research Group, Universitat de les Illes Balears, 07122 Palma, Spain.
Int J Mol Sci. 2024 Nov 30;25(23):12899. doi: 10.3390/ijms252312899.
Maternal unbalanced diets cause adverse metabolic programming and affect the offspring's liver microRNA (miRNA) profile. The liver is a site of β-carotene (BC) metabolism and a target of BC action. We studied the interaction of maternal Western diet (WD) and early-life BC supplementation on the epigenetic remodeling of offspring's liver microRNAs. Mouse offspring of WD-fed mothers were given a daily placebo (controls) or BC during suckling. Biometric parameters and liver miRNAome by microarray hybridization were analyzed in newly weaned animals. BC sex-dependently impacted the liver triacylglycerol content. The liver miRNAome was also differently affected in male and female offspring, with no overlap in differentially expressed (DE) miRNAs between sexes and more impact in females. Bioinformatic analysis of DE miRNA predicted target genes revealed enrichment in biological processes/pathways related to metabolic processes, regulation of developmental growth and circadian rhythm, liver homeostasis and metabolism, insulin resistance, and neurodegeneration, among others, with differences between sexes. Fifty-five percent of the overlapping target genes in both sexes identified were targeted by DE miRNAs changed in opposite directions in males and females. The results identify sex-dependent responses of the liver miRNA expression profile to BC supplementation during suckling and may sustain further investigations regarding the long-term impact of early postnatal life BC supplementation on top of an unbalanced maternal diet.
母体不均衡饮食会导致不良的代谢编程,并影响后代肝脏微小RNA(miRNA)谱。肝脏是β-胡萝卜素(BC)代谢的场所,也是BC作用的靶点。我们研究了母体西方饮食(WD)与早期BC补充对后代肝脏微小RNA表观遗传重塑的相互作用。给喂食WD的母鼠所产的小鼠后代在哺乳期间每日给予安慰剂(对照组)或BC。对刚断奶的动物分析了生物特征参数和通过微阵列杂交检测的肝脏miRNA组。BC对肝脏三酰甘油含量的影响存在性别差异。肝脏miRNA组在雄性和雌性后代中也受到不同影响,两性之间差异表达(DE)的miRNA没有重叠,且对雌性的影响更大。对DE miRNA预测靶基因的生物信息学分析揭示了在与代谢过程、发育生长调节和昼夜节律、肝脏内环境稳定和代谢、胰岛素抵抗以及神经退行性变等相关的生物学过程/途径中存在富集,两性之间存在差异。在两性中鉴定出的重叠靶基因中有55%被DE miRNA靶向,而这些DE miRNA在雄性和雌性中呈相反方向变化。这些结果确定了哺乳期间肝脏miRNA表达谱对BC补充的性别依赖性反应,并可能支持进一步研究产后早期BC补充在不均衡母体饮食基础上的长期影响。