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5'-腺苷酸激活蛋白激酶α调节应激颗粒的生物合成。

5'-AMP-activated protein kinase alpha regulates stress granule biogenesis.

作者信息

Mahboubi Hicham, Barisé Ramla, Stochaj Ursula

机构信息

Department of Physiology, McGill University, 3655 Promenade Sir William Osler, Montreal, QC H3G 1Y6, Canada.

Department of Physiology, McGill University, 3655 Promenade Sir William Osler, Montreal, QC H3G 1Y6, Canada.

出版信息

Biochim Biophys Acta. 2015 Jul;1853(7):1725-37. doi: 10.1016/j.bbamcr.2015.03.015. Epub 2015 Mar 31.

Abstract

Stress granule (SG) assembly represents a conserved eukaryotic defense strategy against various insults. Although essential for the ability to cope with deleterious conditions, the signaling pathways controlling SG formation are not fully understood. The energy sensor AMP-activated protein kinase (AMPK) is critical for the cellular stress response. Human cells produce two AMPK catalytic α-subunits with not only partially overlapping, but also unique functions. Here, we provide direct support for structural and functional links between AMPK-α isoforms and SGs. As such, several stressors promote SG association of AMPK-α2, but not AMPK-α1. Multiple lines of evidence link AMPK activity to SG biogenesis. First, pharmacological kinase inhibition interfered with SG formation. Second, AMPK-α knockdown combined with in-depth quantitative SG analysis revealed isoform-specific changes of SG characteristics. Third, overexpression of mutant α-subunits further substantiated that AMPK regulates SG parameters. Finally, we identified the SG-nucleating protein G3BP1 as an AMPK-α2 binding partner. This interaction is stimulated by stress and notably occurs in SGs. Collectively, our data define the master metabolic regulator AMPK as a novel SG constituent that also controls their biogenesis.

摘要

应激颗粒(SG)组装是真核生物针对各种损伤的一种保守防御策略。尽管对于应对有害条件的能力至关重要,但控制SG形成的信号通路尚未完全了解。能量传感器AMP激活的蛋白激酶(AMPK)对细胞应激反应至关重要。人类细胞产生两种AMPK催化α亚基,它们不仅具有部分重叠的功能,还具有独特的功能。在这里,我们为AMPK-α亚型与SG之间的结构和功能联系提供了直接支持。因此,几种应激源促进了AMPK-α2与SG的结合,但不促进AMPK-α1与SG的结合。多条证据将AMPK活性与SG生物合成联系起来。首先,药理学激酶抑制干扰了SG的形成。其次,AMPK-α敲低结合深入的定量SG分析揭示了SG特征的亚型特异性变化。第三,突变α亚基的过表达进一步证实了AMPK调节SG参数。最后,我们确定SG成核蛋白G3BP1是AMPK-α2的结合伙伴。这种相互作用受到应激的刺激,并且特别发生在SG中。总体而言,我们的数据将主要代谢调节因子AMPK定义为一种新型SG成分,它也控制着SG的生物合成。

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