Comparative analysis of acute eccentric contraction-induced changes to the skeletal muscle transcriptome in young and aged mice and humans.

Jake R Boykin, Jennifer L Steiner, Grant R Laskin, Michael D Roberts, Cynthia Vied, Craig Rg Willis, Timothy Etheridge, Bradley S Gordon
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Abstract

Adaptations to skeletal muscle following resistance exercise are due in part to changes to the skeletal muscle transcriptome. While transcriptional changes in response to resistance exercise occur in young and aged muscle, aging alters this response. Rodent models have served great utility in defining regulatory factors that underscore the influence of mechanical load and aging on changes to skeletal muscle phenotype. Unilateral eccentric contractions in young and aged rodents are widely used to model resistance exercise in humans. However, the extent to which unilateral eccentric contractions in young and aged rodents mimics the transcriptional response in humans remains unknown. We re-analyzed two publicly available RNA sequencing datasets from young and aged mice and humans that were subjected to acute eccentric contractions to define key similarities and differences to the muscle transcriptional response following this exercise modality. The effect of aging on the number of contraction-sensitive genes, the distribution patterns of those genes into unique/common categories, and the cellular pathways associated with the differentially expressed genes (DEGs) were similar in mice and humans. However, there was little overlap between species when comparing specific contraction-sensitive DEGs within the same age group. There were strong intraspecies relationships for the common transcription factors predicted to influence the contraction-sensitive gene sets, whereas interspecies relationships were weak. Overall, these data demonstrate key similarities between mice and humans for the contraction-induced changes to the muscle transcriptome, but we posit species-specific responses exist and should be taken into consideration when attempting to translate rodent eccentric exercise models.

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比较分析急性偏心收缩引起的年轻小鼠、老年小鼠和人类骨骼肌转录组的变化。
阻力运动后骨骼肌的适应性部分归因于骨骼肌转录组的变化。虽然年轻和衰老的肌肉都会发生响应阻力运动的转录变化,但衰老会改变这种响应。啮齿动物模型在确定调控因素方面发挥了重要作用,这些因素强调了机械负荷和衰老对骨骼肌表型变化的影响。年轻和衰老啮齿类动物的单侧偏心收缩被广泛用于模拟人类的阻力运动。然而,年轻啮齿类动物和老年啮齿类动物的单侧偏心收缩在多大程度上模拟了人类的转录反应仍是未知数。我们重新分析了两个公开的 RNA 测序数据集,它们分别来自年轻小鼠、老年小鼠和接受急性偏心收缩的人类,以确定这种运动方式后肌肉转录反应的主要相似点和不同点。在小鼠和人类中,衰老对收缩敏感基因数量的影响、这些基因在独特/常见类别中的分布模式以及与差异表达基因(DEGs)相关的细胞通路是相似的。然而,在比较同一年龄组的特定收缩敏感 DEGs 时,物种间几乎没有重叠。在预测会影响收缩敏感基因集的共同转录因子方面,种内关系较强,而种间关系较弱。总之,这些数据表明小鼠和人类在肌肉转录组收缩诱导的变化方面存在关键的相似性,但我们认为存在物种特异性反应,在尝试转化啮齿类动物偏心运动模型时应加以考虑。
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来源期刊
CiteScore
5.30
自引率
3.60%
发文量
145
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Regulatory, Integrative and Comparative Physiology publishes original investigations that illuminate normal or abnormal regulation and integration of physiological mechanisms at all levels of biological organization, ranging from molecules to humans, including clinical investigations. Major areas of emphasis include regulation in genetically modified animals; model organisms; development and tissue plasticity; neurohumoral control of circulation and hypertension; local control of circulation; cardiac and renal integration; thirst and volume, electrolyte homeostasis; glucose homeostasis and energy balance; appetite and obesity; inflammation and cytokines; integrative physiology of pregnancy-parturition-lactation; and thermoregulation and adaptations to exercise and environmental stress.
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