School of Anesthesiology, Weifang Medical University, Weifang 261053, China.
Department of Orthopedics, Affiliated Hospital of Weifang Medical University, Weifang 261035, China.
Gene. 2024 May 15;906:148217. doi: 10.1016/j.gene.2024.148217. Epub 2024 Feb 9.
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.
细胞坏死已被证明有助于心肌缺血再灌注损伤(MIRI)。本研究旨在通过 RNA 测序,在大鼠 MIRI 中深入了解细胞坏死的信号通路。通过结扎左前降支冠状动脉 30 分钟诱导雄性大鼠发生 MIRI,然后再灌注 120 分钟。进行 RNA 测序以获得 MIRI 组和用坏死抑制剂-1(Nec-1,细胞坏死的抑制剂)处理的 MIRI 组的 mRNA 图谱。然后鉴定差异表达基因(DEGs)。DEGs 主要富集在 TNF-α信号通路、MAPK 信号通路和细胞因子-细胞因子受体通路中。大多数结果与 Thumpd3、Egr2、Dot1l、Cyp1a1、Dbnl 等基因有关,这些基因主要调节炎症反应和细胞凋亡,尤其是在心肌中。上述结果表明,Nec-1 可能通过上述基因参与调节细胞坏死和炎症反应。