坏死性下垂
生物
再灌注损伤
转录组
信号转导
RNA序列
细胞因子
核糖核酸
细胞生物学
信使核糖核酸
MAPK/ERK通路
细胞凋亡
肿瘤坏死因子α
基因
缺血
基因表达
癌症研究
免疫学
程序性细胞死亡
内科学
遗传学
医学
作者
Yijia Zhang,Qingbiao Song,E Sihan,Xuehao Guan,Zhiyu Zhang,Zhaodong Juan,Xiaotong Sun,Yingxia Liang
出处
期刊:Gene
[Elsevier]
日期:2024-02-09
卷期号:906: 148217-148217
被引量:1
标识
DOI:10.1016/j.gene.2024.148217
摘要
Necroptosis has been shown to contribute to myocardial ischemia reperfusion injury (MIRI). This study aims to gain new insights into the signaling pathway of necroptosis in rat MIRI using RNA sequencing. MIRI was induced in male rats by ligating the left anterior descending coronary artery for 30 min, followed by reperfusion for 120 min. RNA sequencing was performed to obtain mRNA profiles of MIRI group and MIRI group treated with necrostatin-1 (Nec-1,an inhibitor of necroptosis). Differentially expressed genes (DEGs) were then identified. The DEGs were prominently enriched in the TNF-α signaling pathway, the MAPK signaling pathway and cytokine-cytokine receptor pathways. The majority of the results were associated with genes like Thumpd3,Egr2,Dot1l,Cyp1a1,Dbnl,which primarily regulate inflammatory response and apoptosis, particularly in myocardium. The above results suggested that Nec-1 might be involved in the regulation of necroptosis and the inflammatory response through the above-mentioned genes.
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