Zapata-Bustos Rocio, Finlayson Jean, Langlais Paul R, Coletta Dawn K, Luo Moulun, Grandjean Danielle, De Filippis Elena A, Mandarino Lawrence
Division of Endocrinology, Department of Medicine, University of Arizona, Tucson, AZ, United States.
Center for Disparities in Diabetes, Obesity and Metabolism, University of Arizona Health Sciences, Tucson, AZ, United States.
Front Physiol. 2021 Apr 7;12:649461. doi: 10.3389/fphys.2021.649461. eCollection 2021.
Insulin resistant muscle is resistant to gene expression changes induced by acute exercise. This study was undertaken to identify transcription factors that differentially respond to exercise in insulin resistance. Candidate transcription factors were identified from analysis of 5'-untranslated regions (5'-UTRs) of exercise responsive genes and from analysis of the 5'-UTRs of genes coding for proteins that differ in abundance in insulin resistance.
Twenty participants took part in this study. Insulin sensitivity was assessed by an euglycemic clamp. Participants were matched for aerobic capacity and performed a single 48 min bout of exercise with sets at 70 and 90% of maximum heart rate. Muscle biopsies were obtained at resting conditions, 30 min and 24 h after exercise. Global proteomics analysis identified differentially abundant proteins in muscle. The 5'-UTRs of genes coding for significant proteins were subjected to transcription factor enrichment analysis to identify candidate transcription factors. Q-rt-PCR to determine expression of candidate transcription factors was performed on RNA from resting and post-exercise muscle biopsies; immunoblots quantified protein abundance.
Proteins involved in mitochondrial function, protein targeting and translation, and metabolism were among those significantly different between lean and obese groups. Transcription factor enrichment analysis of genes coding for these proteins revealed new candidate transcription factors to be evaluated along the previously identified factors. Q-rt-PCR analysis of RNA and immunoblot analysis from pre- and post-exercise muscle biopsies revealed several transcription and growth factors that had altered responses to exercise in insulin resistant participants. A significant increase (EGR3 and CTGF) and decrease (RELA and ATF2) in the mRNA expression of transcription and growth factors was found after exercise in the lean group, but not in the obese participants.
These results confirm findings of an association between insulin sensitivity and transcription factor mRNA response to exercise and show that obesity also may be a sufficient prerequisite for exercise resistance. Analysis of the muscle proteome together with determination of effects of exercise on expression of transcription factors suggests that abnormal responses of transcription factors to exercise may be responsible for differences in protein abundances in insulin resistant muscle.
胰岛素抵抗的肌肉对急性运动诱导的基因表达变化具有抗性。本研究旨在确定在胰岛素抵抗中对运动有不同反应的转录因子。通过对运动反应性基因的5'-非翻译区(5'-UTR)分析以及对胰岛素抵抗中丰度不同的蛋白质编码基因的5'-UTR分析来鉴定候选转录因子。
20名参与者参与了本研究。通过正常血糖钳夹评估胰岛素敏感性。参与者根据有氧能力进行匹配,并进行一次48分钟的运动,运动强度为最大心率的70%和90%。在静息状态、运动后30分钟和24小时获取肌肉活检样本。全局蛋白质组学分析确定了肌肉中丰度不同的蛋白质。对显著蛋白质编码基因的5'-UTR进行转录因子富集分析以鉴定候选转录因子。对静息和运动后肌肉活检样本的RNA进行定量逆转录聚合酶链反应(Q-rt-PCR)以确定候选转录因子的表达;免疫印迹法定量蛋白质丰度。
参与线粒体功能、蛋白质靶向与翻译以及代谢的蛋白质在瘦组和肥胖组之间存在显著差异。对这些蛋白质编码基因的转录因子富集分析揭示了新的候选转录因子,需与先前鉴定的因子一起进行评估。对运动前后肌肉活检样本的RNA进行Q-rt-PCR分析以及免疫印迹分析发现,在胰岛素抵抗的参与者中,有几种转录和生长因子对运动的反应发生了改变。运动后,瘦组转录和生长因子的mRNA表达显著增加(EGR3和CTGF)及减少(RELA和ATF2),但肥胖参与者未出现这种情况。
这些结果证实了胰岛素敏感性与转录因子mRNA对运动的反应之间存在关联的发现,并表明肥胖也可能是运动抵抗的充分先决条件。对肌肉蛋白质组的分析以及运动对转录因子表达影响的测定表明,转录因子对运动的异常反应可能是胰岛素抵抗肌肉中蛋白质丰度差异的原因。