Beck Emily A, Hetrick Byron, Nassar Luis, Turnbull Douglas W, Dean Tyler A, Gannon Maureen, Aagaard Kjersti M, Wesolowski Stephanie R, Friedman Jacob E, Kievit Paul, McCurdy Carrie E
bioRxiv. 2024 May 21:2024.05.17.594191. doi: 10.1101/2024.05.17.594191.
Early-life exposure to maternal obesity or a maternal calorically dense Western-style diet (WSD) is strongly associated with a greater risk of metabolic diseases in offspring, most notably insulin resistance and metabolic dysfunction-associated steatotic liver disease (MASLD). Prior studies in our well-characterized Japanese macaque model demonstrated that offspring of dams fed a WSD, even when weaned onto a control (CTR) diet, had reductions in skeletal muscle mitochondrial metabolism and increased skeletal muscle insulin resistance compared to offspring of dams on CTR diet. In the current study, we employed a nested design to test for differences in gene expression in skeletal muscle from lean 3-year-old adolescent offspring from dams fed a maternal WSD in both the presence and absence of maternal obesity or lean dams fed a CTR diet. We included offspring weaned to both a WSD or CTR diet to further account for differences in response to post-weaning diet and interaction effects between diets. Overall, we found that a maternal WSD fed to dams during pregnancy and lactation was the principal driver of differential gene expression (DEG) in offspring muscle at this time point. We identified key gene pathways important in insulin signaling including PI3K-Akt and MAP-kinase, regulation of muscle regeneration, and transcription-translation feedback loops, in both male and female offspring. Muscle DEG showed no measurable difference between offspring of obese dams on WSD compared to those of lean dams fed WSD. A post-weaning WSD effected offspring transcription only in individuals from the maternal CTR diet group but not in maternal WSD group. Collectively, we identify that maternal diet composition has a significant and lasting impact on offspring muscle transcriptome and influences later transcriptional response to WSD in muscle, which may underlie the increased metabolic disease risk in offspring.
生命早期暴露于母体肥胖或母体高热量西式饮食(WSD)与后代患代谢性疾病的风险增加密切相关,最显著的是胰岛素抵抗和代谢功能障碍相关脂肪性肝病(MASLD)。我们在特征明确的日本猕猴模型上进行的先前研究表明,喂食WSD的母猴的后代,即使断奶后改为对照(CTR)饮食,与喂食CTR饮食的母猴的后代相比,骨骼肌线粒体代谢降低,骨骼肌胰岛素抵抗增加。在本研究中,我们采用嵌套设计,测试来自喂食母体WSD的母猴的3岁瘦青少年后代在有或没有母体肥胖情况下,以及喂食CTR饮食的瘦母猴的后代骨骼肌中基因表达的差异。我们纳入了断奶后改为WSD或CTR饮食的后代,以进一步说明断奶后饮食反应的差异以及饮食之间的相互作用。总体而言,我们发现孕期和哺乳期母猴喂食WSD是此时后代肌肉中差异基因表达(DEG)的主要驱动因素。我们在雄性和雌性后代中都确定了胰岛素信号传导中重要的关键基因途径,包括PI3K-Akt和丝裂原活化蛋白激酶、肌肉再生的调节以及转录-翻译反馈环。与喂食WSD的瘦母猴的后代相比,喂食WSD的肥胖母猴的后代的肌肉DEG没有可测量的差异。断奶后WSD仅影响来自母体CTR饮食组个体的后代转录,而不影响母体WSD组。总体而言,我们确定母体饮食组成对后代肌肉转录组有显著且持久的影响,并影响肌肉对WSD的后续转录反应,这可能是后代代谢疾病风险增加的基础。