The Time Sequence of Gene Expression Changes after Spinal Cord Injury

被引:5
|
作者
Mun, Seyoung [1 ,2 ,3 ]
Han, Kyudong [3 ,4 ]
Hyun, Jung Keun [1 ,2 ,5 ,6 ]
机构
[1] Dankook Univ, Dept Nanobiomed Sci, Cheonan 31116, South Korea
[2] Dankook Univ, BK21 NBM Global Res Ctr Regenerat Med, Cheonan 31116, South Korea
[3] Dankook Univ, Ctr Bio Med Engn Core Facil, Cheonan 31116, South Korea
[4] Dankook Univ, Coll Sci & Technol, Dept Microbiol, Cheonan 31116, South Korea
[5] Dankook Univ, Coll Med, Dept Rehabil Med, Cheonan 31116, South Korea
[6] Dankook Univ, Inst Tissue Regenerat Engn ITREN, Cheonan 31116, South Korea
基金
新加坡国家研究基金会;
关键词
spinal cord injury; RNA sequencing; time sequence; small molecules; gene ontology; RNA-SEQ; DOUBLE-BLIND; RECOVERY; SURGERY; DEXTROMETHORPHAN; NEUROPROTECTION; INTERVENTION; TRANSLATION; APOMORPHINE; GLUTAMATE;
D O I
10.3390/cells11142236
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Gene expression changes following spinal cord injury (SCI) are time-dependent, and an accurate understanding of these changes can be crucial in determining time-based treatment options in a clinical setting. We performed RNA sequencing of the contused spinal cord of rats at five different time points from the very acute to chronic stages (1 hour, 1 day, 1 week, 1 month, and 3 months) following SCI. We identified differentially expressed genes (DEGs) and Gene Ontology (GO) terms at each time point, and 14,257 genes were commonly expressed at all time points. The biological process of the inflammatory response was increased at 1 hour and 1 day, and the cellular component of the integral component of the synaptic membrane was increased at 1 day. DEGs associated with cell activation and the innate immune response were highly enriched at 1 week and 1 month, respectively. A total of 2841 DEGs were differentially expressed at any of the five time points, and 18 genes (17 upregulated and 1 downregulated) showed common expression differences at all time points. We found that interleukin signaling, neutrophil degranulation, eukaryotic translation, collagen degradation, LGI-ADAM interactions, GABA receptor, and L1CAM-ankyrin interactions were prominent after SCI depending on the time post injury. We also performed gene-drug network analysis and found several potential antagonists and agonists which can be used to treat SCI. We expect to discover effective treatments in the clinical field through further studies revealing the efficacy and safety of potential drugs.
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页数:23
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