School of Forensic Medicine, Shanxi Medical University, Jinzhong 030604, Shanxi, China.
Key Laboratory of Evidence Science, China University of Political Science and law, Beijing, China.
Biosci Rep. 2021 Jan 29;41(1). doi: 10.1042/BSR20203699.
Muscle trauma frequently occurs in daily life. However, the molecular mechanisms of muscle healing, which partly depend on the extent of the damage, are not well understood. The present study aimed to investigate gene expression profiles following mild and severe muscle contusion, and to provide more information about the molecular mechanisms underlying the repair process. A total of 33 rats were divided randomly into control (n=3), mild contusion (n=15), and severe contusion (n=15) groups; the contusion groups were further divided into five subgroups (1, 3, 24, 48, and 168 h post-injury; n=3 per subgroup). A total of 2844 and 2298 differentially expressed genes (DEGs) were identified using microarray analyses in the mild and severe contusions, respectively. From the analysis of the 1620 coexpressed genes in mildly and severely contused muscle, we discovered that the gene profiles in functional modules and temporal clusters were similar between the mild and severe contusion groups; moreover, the genes showed time-dependent patterns of expression, which allowed us to identify useful markers of wound age. The functional analyses of genes in the functional modules and temporal clusters were performed, and the hub genes in each module-cluster pair were identified. Interestingly, we found that genes down-regulated at 24-48 h were largely associated with metabolic processes, especially of the oxidative phosphorylation (OXPHOS), which has been rarely reported. These results improve our understanding of the molecular mechanisms underlying muscle repair, and provide a basis for further studies of wound age estimation.
肌肉创伤在日常生活中经常发生。然而,肌肉愈合的分子机制部分取决于损伤的程度,目前还不是很清楚。本研究旨在探讨轻度和重度肌肉挫伤后的基因表达谱,为修复过程的分子机制提供更多信息。总共 33 只大鼠随机分为对照组(n=3)、轻度挫伤组(n=15)和重度挫伤组(n=15);挫伤组进一步分为五个亚组(伤后 1、3、24、48 和 168 小时;n=3 个/亚组)。通过微阵列分析,分别在轻度和重度挫伤中鉴定出 2844 和 2298 个差异表达基因(DEGs)。通过分析轻度和重度挫伤肌肉中 1620 个共表达基因,我们发现功能模块和时间聚类中的基因图谱在轻度和重度挫伤组之间相似;此外,基因表现出时间依赖性表达模式,这使我们能够识别伤口年龄的有用标志物。对功能模块和时间聚类中的基因进行功能分析,并鉴定每个模块-聚类对中的枢纽基因。有趣的是,我们发现 24-48 小时下调的基因主要与代谢过程有关,特别是氧化磷酸化(OXPHOS),这很少有报道。这些结果提高了我们对肌肉修复分子机制的理解,并为进一步研究伤口年龄估计提供了基础。