Literature DB >> 33398324

Insight into molecular profile changes after skeletal muscle contusion using microarray and bioinformatics analyses.

Na Li1, Ru-Feng Bai2,3, Chun Li1, Li-Hong Dang1, Qiu-Xiang Du1, Qian-Qian Jin1, Jie Cao1, Ying-Yuan Wang1, Jun-Hong Sun1.   

Abstract

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.
© 2021 The Author(s).

Entities:  

Keywords:  Skeletal muscle healing; bioinformatics analysis; gene expression profile; microarray; wound age

Mesh:

Year:  2021        PMID: 33398324      PMCID: PMC7816072          DOI: 10.1042/BSR20203699

Source DB:  PubMed          Journal:  Biosci Rep        ISSN: 0144-8463            Impact factor:   3.840


  45 in total

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7.  Platelet-rich plasma reduces the oxidative damage determined by a skeletal muscle contusion in rats.

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8.  The intensity of the inflammatory response in experimental porcine bruises depends on time, anatomical location and sampling site.

Authors:  Kristiane Barington; Kerstin Skovgaard; Nicole Lind Henriksen; Anne Sofie Boyum Johansen; Henrik Elvang Jensen
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Journal:  Skelet Muscle       Date:  2016-11-08       Impact factor: 4.912

Review 10.  Vitality and wound-age estimation in forensic pathology: review and future prospects.

Authors:  Na Li; Qiuxiang Du; Rufeng Bai; Junhong Sun
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Review 1.  The Role of miRNAs as New Molecular Biomarkers for Dating the Age of Wound Production: A Systematic Review.

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2.  Contusion concomitant with ischemia injury aggravates skeletal muscle necrosis and hinders muscle functional recovery.

Authors:  Peijun Deng; Shuai Qiu; Fawei Liao; Yifei Jiang; Canbin Zheng; Qingtang Zhu
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  2 in total

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