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首页> 外文期刊>American Journal of Physiology >75-kDa glucose-regulated protein (GRP75) is a novel molecular signature for heat stress response in avian species
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75-kDa glucose-regulated protein (GRP75) is a novel molecular signature for heat stress response in avian species

机译:75-KDA葡萄糖调节蛋白(GRP75)是一种用于禽类中的热应激反应的新型分子签名

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摘要

Glucose-regulated protein 75 (GRP75) was first characterized in mammals as a heat shock protein-70 (HSP70) family stress chaperone based on its sequence homology. Extensive studies in mammals showed that GRP75 is induced by various stressors such as glucose deprivation, oxidative stress, and hypoxia, although it remained unresponsive to the heat shock. Such investigations are scarce in avian (nonmammalian) species. We here identified chicken GRP75 by using immunoprecipitation assay integrated with LC-MS/MS, and found that its amino acid sequence is conserved with high homology (52.5%) to the HSP70 family. Bioinformatics and 3D-structure prediction indicate that, like most HSPs, chicken GRP75 has two principal domains (the NH2-terminal ATPase and COOH-terminal region). Immunofluorescence staining shows that GRP75 is localized predominantly in the avian myoblast and hepatocyte mitochondria. Heat stress exposure upregulates GRP75 expression in a species-, genotype-, and tissue-specific manner. Overexpression of GRP75 reduces avian cell viability, and blockade of GRP75 by its small molecular inhibitor MKT-077 rescues avian cell viability during heat stress. Taken together, this is the first evidence showing that chicken GRP75, unlike its mammalian ortholog, is responsive to heat shock and plays a key role in cell survival/death pathways. Since modern avian species have high metabolic rates and are sensitive to high environmental temperature, GRP75 could open new vistas in mechanistic understanding of heat stress responses and thermotolerance in avian species.
机译:葡萄糖调节蛋白质75(GRP75)首先在哺乳动物中以热休克蛋白-70(HSP70)家族应激伴侣的特征在于其序列同源性。哺乳动物的广泛研究表明,GRP75由各种压力源诱导,例如葡萄糖剥夺,氧化应激和缺氧,但它对热休克保持不反应。这种调查在禽(非含哺乳动物)物种中稀缺。我们通过使用与LC-MS / MS集成的免疫沉淀法测定来确定鸡GRP75,发现其氨基酸序列具有高同源性(52.5%)至HSP70家族。生物信息学和3D结构预测表明,与大多数HSP一样,鸡GRP75具有两个主域(NH2末端ATP酶和COOH-末端区域)。免疫荧光染色表明GRP75主要位于禽肌细胞和肝细胞线粒体中。热应力曝光以物种,基因型和组织特异性方式提高GRP75表达。 GRP75的过度表达降低了禽细胞活力,并通过其小分子抑制剂MKT-077抵抗GRP75的阻断在热应激期间抵押禽细胞活力。在一起,这是第一个显示鸡Grp75与其哺乳动物直脑不同的证据,对热休克响应,并在细胞存活/死亡途径中起着关键作用。由于现代禽类具有高的代谢速率,并且对高环境温度敏感,GRP75可以在禽类种类的热应激反应和热能的机械理解中开辟新的远程。

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