Zheng Jia, Xiao Xinhua, Zhang Qian, Wang Tong, Yu Miao, Xu Jianping
Department of Endocrinology, Key Laboratory of Endocrinology, Ministry of Health, Peking Union Medical College Hospital, Diabetes Research Center of Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Nutrients. 2017 Feb 27;9(3):205. doi: 10.3390/nu9030205.
Emerging studies revealed that maternal protein restriction was associated with increased risk of type 2 diabetes mellitus in adulthood. However, the mechanisms of its effects on offspring, especially during early life of offspring, are poorly understood. Here, it is hypothesized that impaired metabolic health in offspring from maternal low-protein diet (LPD) is associated with perturbed miRNAs expression in offspring as early as the weaning age. We examined the metabolic effects on the C57BL/6J mice male offspring at weaning from dams fed with LPD or normal chow diet (NCD) throughout pregnancy and lactation. Maternal LPD feeding impaired metabolic health in offspring. Microarray profiling indicated that mmu-miR-615, mmu-miR-124, mmu-miR-376b, and mmu-let-7e were significantly downregulated, while, mmu-miR-708 and mmu-miR-879 were upregulated in LPD offspring. Bioinformatic analysis showed target genes were mapped to inflammatory-related pathways. Serum tumor necrosis factor-α (TNF-α) levels were higher and interleukin 6 (IL-6) had a tendency to be elevated in the LPD group. Finally, both mRNA and protein levels of IL-6 and TNF-α were significantly increased in the LPD group. Our findings provide novel evidence that maternal LPD can regulate miRNAs expression, which may be associated with chronic inflammation status and metabolic health in offspring as early as the weaning age.
新兴研究表明,孕期蛋白质摄入受限与成年后患2型糖尿病的风险增加有关。然而,其对后代,尤其是后代早期生活的影响机制却知之甚少。在此,我们推测,母亲低蛋白饮食(LPD)的后代代谢健康受损与断奶期后代中微小RNA(miRNA)表达紊乱有关。我们研究了在整个怀孕和哺乳期喂食LPD或正常对照饮食(NCD)的母鼠所产雄性C57BL/6J小鼠后代在断奶时的代谢影响。母亲喂食LPD会损害后代的代谢健康。微阵列分析表明,mmu-miR-615、mmu-miR-124、mmu-miR-376b和mmu-let-7e在LPD组后代中显著下调,而mmu-miR-708和mmu-miR-879则上调。生物信息学分析显示,靶基因映射到炎症相关途径。LPD组血清肿瘤坏死因子-α(TNF-α)水平较高,白细胞介素6(IL-6)有升高趋势。最后,LPD组中IL-6和TNF-α的mRNA和蛋白水平均显著升高。我们的研究结果提供了新的证据,表明母亲LPD可调节miRNA表达,这可能与断奶期后代的慢性炎症状态和代谢健康有关。