在心肌细胞损伤中,ATF3通过内细胞网膜应激调节SPHK1
Huiling Chen1, Suxin Luo1, Huamei Chen2
1Division of Cardiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, P.R. China.
Immunity, inflammation and disease
|September 29, 2023
概括
降低调节的激活转录因子3 (ATF3) 降低了斯芬戈辛激酶-1 (SPHK1) 的表达,从而在心肌梗塞 (MI) 期间保护心肌细胞损伤和内质网膜 (ER) 应激. 这一发现为心脏病提供了潜在的治疗点.
科学领域:
- 心血管生物学 心血管生物学
- 分子心脏病学分子心脏病学
- 细胞应激反应的应激反应
背景情况:
- 细胞内膜网膜 (ER) 的压力与心脏病理有关.
- 氨酸激酶-1 (SPHK1) 在心脏功能中起作用,但其在ER压力中的作用尚不清楚.
研究的目的:
- 研究SPHK1在心肌梗塞 (MI) 期间影响心肌细胞中ER应激的机制.
主要方法:
- 与心脏病相关数据集的差异基因表达分析.
- 在体外 (缺氧-葡萄糖的HL-1细胞) 和体内 (MI小鼠模型) 的研究.
- 基因表达操纵 (shRNA,过度表达),细胞活力测试,细胞亡和氧化应激检测,组织学染色和ELISA用于炎症标志物.
主要成果:
- 激活转录因子3 (ATF3) 和SPHK1在MI模型中被上调.
- 降低ATF3调节降低了SPHK1转录,改善了细胞活力,减少了细胞亡,氧化应激和ER应激.
- 在小鼠中抑制ATF3和SPHK1减弱的心肌梗塞大小,纤维化,炎症和ER压力.
结论:
- 降低ATF3调节通过减少SPHK1表达来缓解心肌梗塞中的心肌细胞损伤.
- 针对ATF3-SPHK1轴可能为心肌梗塞提供治疗策略.
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