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Mild heat induces a distinct eustress response in Chinese Hamster Ovary cells but does not induce heat shock protein synthesis

机译:温和的热量在中国仓鼠卵巢细胞中诱导出明显的应激反应但不会诱导热休克蛋白合成

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摘要

The current research on cellular heat stress management focuses on the roles of heat shock proteins (HSPs) and the proteostasis network under severe stress conditions. The mild, fever-type stress and the maintenance of membrane homeostasis are less well understood. Herein, we characterized the acute effect of mild, fever-range heat shock on membrane organization, and HSP synthesis and localization in two mammalian cell lines, to delineate the role of membranes in the sensing and adaptation to heat. A multidisciplinary approach combining ultrasensitive fluorescence microscopy and lipidomics revealed the molecular details of novel cellular “eustress”, when cells adapt to mild heat by maintaining membrane homeostasis, activating lipid remodeling, and redistributing chaperone proteins. Notably, this leads to acquired thermotolerance in the complete absence of the induction of HSPs. At higher temperatures, additional defense mechanisms are activated, including elevated expression of molecular chaperones, contributing to an extended stress memory and acquired thermotolerance.
机译:当前对细胞热应激管理的研究集中在严重应激条件下热休克蛋白(HSPs)和蛋白稳定网络的作用。轻度,发烧型应激和膜稳态的维持尚不清楚。在本文中,我们表征了轻度,发烧范围的热休克对膜组织以及两种哺乳动物细胞系中HSP合成和定位的急性影响,以描述膜在感测和适应热中的作用。当细胞通过维持膜稳态,激活脂质重塑和重新分配伴侣蛋白来适应温和的热量时,采用超灵敏荧光显微镜和脂质组学的多学科方法揭示了新型细胞“应激”的分子细节。值得注意的是,这导致在完全不诱导HSP的情况下获得了耐热性。在更高的温度下,其他防御机制被激活,包括分子伴侣分子的高表达,有助于延长压力记忆和获得的耐热性。

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