Beck Emily A, Hetrick Byron, Nassar Luis, Turnbull Douglas W, Dean Tyler A, Takahashi Diana L, Gannon Maureen, Wesolowski Stephanie R, Aagaard Kjersti M, Friedman Jacob E, Kievit Paul, McCurdy Carrie E
Department of Data Science, University of Oregon, Eugene, OR, USA.
Department of Molecular Biosciences, University of Kansas, 5060 Haworth Hall, 1200 Sunnyside Avenue, Lawrence, KS, 66045, USA.
Sci Rep. 2025 Jul 1;15(1):21324. doi: 10.1038/s41598-025-00828-3.
The cellular mechanisms underlying a greater risk of cardiometabolic disease in adult offspring exposed to maternal obesity are not known. Our prior work found reduced skeletal muscle mitochondrial metabolism and insulin sensitivity in offspring exposed to maternal (m) Western-style diet (WD), even when weaned onto a control diet (CD) in Japanese macaques. Here, we performed multiple comparisons of differentially expressed (DE) genes in skeletal muscle from lean juvenile offspring to test hypotheses specific to (1) the lasting effects of maternal diet composition and/or maternal adiposity on gene expression and (2) the transcriptional response to a chronic postweaning (pw)WD with and without prior exposure to mWD. Overall, we identified maternal (m)WD, and not maternal adiposity, as a principal driver of DE in offspring muscle even years after exposure with few differences observed in patterns of DE between offspring of lean vs. obese mWD dams. Transcriptional response to the pwWD was robust in mCD offspring but blunted by mWD, particularly in males, suggesting a potential priming of gene expression. KEGG enrichment analysis and assessment of top DE genes identified changes in key pathways associated with dysregulated metabolism and RNA processing. We conclude that mWD has a significant and lasting impact on offspring gene expression which likely contributes to observed skeletal muscle insulin resistance and metabolic dysregulation in these offspring.
在暴露于母体肥胖的成年后代中,发生心脏代谢疾病风险更高的细胞机制尚不清楚。我们之前的研究发现,即使在日本猕猴断奶后采用对照饮食(CD),暴露于母体西式饮食(WD)的后代骨骼肌线粒体代谢和胰岛素敏感性也会降低。在此,我们对瘦的幼年后代骨骼肌中差异表达(DE)基因进行了多项比较,以检验以下特定假设:(1)母体饮食组成和/或母体肥胖对基因表达的长期影响;(2)断奶后长期(pw)WD且有或无先前暴露于母体WD的转录反应。总体而言,我们确定母体WD而非母体肥胖是后代肌肉中DE的主要驱动因素,即使在暴露数年之后,瘦的与肥胖的母体WD母猴的后代在DE模式上观察到的差异也很少。对pwWD的转录反应在母体CD后代中很强,但被母体WD削弱,尤其是在雄性中,这表明基因表达存在潜在的启动作用。KEGG富集分析和对顶级DE基因的评估确定了与代谢失调和RNA加工相关的关键途径的变化。我们得出结论,母体WD对后代基因表达有显著且持久的影响,这可能导致这些后代出现骨骼肌胰岛素抵抗和代谢失调。