冲击驱动STAT3和JunB介导的协调转录和DNA甲基化反应在内皮
Ramon Bossardi Ramos1, Nina Martino1, Dareen Chuy1
1Department of Molecular and Cellular Physiology, Albany Medical Center, Albany, NY 12208,USA.
Journal of cell science
|September 5, 2023
概括
败血性休克会通过内皮功能障碍导致器官衰竭. 这项研究揭示了由STAT3和JunB介导的IL-6 (IL-6) 信号传递驱动了内皮细胞的表观遗传变化,从而提供了一个新的治疗点.
科学领域:
- 分子生物学分子生物学
- 免疫学 免疫学 免疫学
- 病理生理学 病理生理学
背景情况:
- 内皮功能障碍是败血性休克中器官衰竭的关键驱动因素.
- 这种功能障碍背后的精确分子机制在很大程度上是未知的.
研究的目的:
- 为了阐明内皮细胞对脂聚糖 (LPS) 的转录和表观遗传反应.
- 研究STAT3-SOCS3信号轴和IL-6在调解这些反应中的作用.
主要方法:
- 脂聚糖 (LPS) 在体内和体外的侮辱.
- 转录和表观遗传学分析.
- 基因对STAT3和JunB的破坏.
- 对转录因子参与的生物信息分析.
主要成果:
- 在LPS伤害后的损伤引发了显著的内皮转录和表观遗传变化.
- SOCS3的损失加剧了这些反应,突出了STAT3-SOCS3轴的因果作用.
- 鉴定出IL-6是内皮细胞中这种反应的媒介.
- 通过生物信息学和敲击实验,STAT,AP1 (包括JunB) 和IRF转录因子都受到影响.
结论:
- 内皮细胞对LPS产生协调反应,涉及过度激活的IL-6信号传递.
- 通过STAT3和JunB,这种途径调节了冲击诱导的表观遗传修饰和持续的内皮激活.
- 准IL-6信号传递是一种潜在的治疗策略,可以减轻败血症休克时的血管功能障碍.
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