Suppr超能文献

特征性的细胞外信号调节激酶1/2(ERK1/2)信号动力学将坏死性凋亡与凋亡区分开来。

Characteristic ERK1/2 signaling dynamics distinguishes necroptosis from apoptosis.

作者信息

Sipieter François, Cappe Benjamin, Leray Aymeric, De Schutter Elke, Bridelance Jolien, Hulpiau Paco, Van Camp Guy, Declercq Wim, Héliot Laurent, Vincent Pierre, Vandenabeele Peter, Riquet Franck B

机构信息

Molecular Signaling and Cell Death Unit, Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.

Molecular Signaling and Cell Death Unit, VIB Center for Inflammation Research, Technologiepark 71, Zwijnaarde, 9052 Ghent, Belgium.

出版信息

iScience. 2021 Sep 2;24(9):103074. doi: 10.1016/j.isci.2021.103074. eCollection 2021 Sep 24.

Abstract

ERK1/2 involvement in cell death remains unclear, although many studies have demonstrated the importance of ERK1/2 dynamics in determining cellular responses. To untangle how ERK1/2 contributes to two cell death programs, we investigated ERK1/2 signaling dynamics during hFasL-induced apoptosis and TNF-induced necroptosis in L929 cells. We observed that ERK1/2 inhibition sensitizes cells to apoptosis while delaying necroptosis. By monitoring ERK1/2 activity by live-cell imaging using an improved ERK1/2 biosensor (EKAR4.0), we reported differential ERK1/2 signaling dynamics between cell survival, apoptosis, and necroptosis. We also decrypted a temporally shifted amplitude- and frequency-modulated (AM/FM) ERK1/2 activity profile in necroptosis versus apoptosis. ERK1/2 inhibition, which disrupted ERK1/2 signaling dynamics, prevented TNF and IL-6 gene expression increase during TNF-induced necroptosis. Using an inducible cell line for activated MLKL, the final executioner of necroptosis, we showed ERK1/2 and its distinctive necroptotic ERK1/2 activity dynamics to be positioned downstream of MLKL.

摘要

尽管许多研究已经证明了ERK1/2动力学在决定细胞反应中的重要性,但ERK1/2在细胞死亡中的作用仍不清楚。为了弄清楚ERK1/2如何促成两种细胞死亡程序,我们研究了L929细胞中hFasL诱导的凋亡和TNF诱导的坏死性凋亡过程中的ERK1/2信号动力学。我们观察到,ERK1/2抑制使细胞对凋亡敏感,同时延迟坏死性凋亡。通过使用改进的ERK1/2生物传感器(EKAR4.0)进行活细胞成像来监测ERK1/2活性,我们报道了细胞存活、凋亡和坏死性凋亡之间不同的ERK1/2信号动力学。我们还解密了坏死性凋亡与凋亡过程中时间上偏移的幅度和频率调制(AM/FM)ERK1/2活性谱。ERK1/2抑制破坏了ERK1/2信号动力学,阻止了TNF诱导的坏死性凋亡过程中TNF和IL-6基因表达的增加。使用一种可诱导的细胞系来激活坏死性凋亡的最终执行者MLKL,我们发现ERK1/2及其独特的坏死性凋亡ERK1/2活性动力学位于MLKL的下游。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a378/8449238/0d09ee180dd0/fx1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验