Stress-Induced Accumulation of HnRNP K into Stress Granules.

Jayoung Kim, Austin Yeon, Woong-Ki Kim, Khae-Hawn Kim, Takbum Ohn
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Abstract

Stress granules (SGs) are cytoplasmic aggregates to reprogram gene expression in response to cellular stimulus. Here, we show that while SGs are being assembled in response to clotrimazole, an antifungal medication heterogeneous nuclear ribonucleoprotein (hnRNP) K, an RNA-binding protein that mediates translational silencing of mRNAs, is rapidly accumulated in SGs in U-2OS osteosarcoma cells. Forced expression of hnRNP K induces resistance to clotrimazole-induced apoptosis. Erk/MAPK is transiently activated in response to clotrimazole, and pharmacological suppression of the Erk/MAPK pathway sensitizes the cells to apoptosis. Inhibition of the Erk/MAPK pathway promotes the assembly of SGs. These results suggest that dynamic cytoplasmic formation of SGs and hnRNP K relocation to SGs may be defensive mechanisms against clotrimazole-induced apoptosis in U-2OS osteosarcoma cells.

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应力诱导的HnRNP - K在应力颗粒中的积累
应激颗粒(SG)是细胞质聚集体,用于响应细胞刺激重新编程基因表达。在这里,我们发现,当SGs对克霉唑产生反应时,一种抗真菌药物异质性核核糖核蛋白(hnRNP)K,一种介导mRNA翻译沉默的RNA结合蛋白,在U-2OS骨肉瘤细胞的SGs中快速积累。hnRNP K的强制表达诱导对克霉唑诱导的细胞凋亡的抗性。Erk/MAPK在对克霉唑的反应中被瞬时激活,并且对Erk/MAPK通路的药理学抑制使细胞对凋亡敏感。Erk/MAPK通路的抑制促进SG的组装。这些结果表明,在U-2OS骨肉瘤细胞中,SGs的动态细胞质形成和hnRNP K向SGs的迁移可能是对抗克霉唑诱导的细胞凋亡的防御机制。
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