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镍中毒对大鼠器官以及COS-7、HepG2和A549细胞系中72/73 kDa和94 kDa应激蛋白表达模式的影响。

Effects of nickel poisoning on expression pattern of the 72/73 and 94 kDa stress proteins in rat organs and in the COS-7, HepG2, and A549 cell lines.

作者信息

Hfaiedh N, Allagui M S, El Feki A, Gaubin Y, Murat J C, Soleilhavoup J P, Croute F

机构信息

Laboratoire d'Ecophysiologie Animale, Faculté des Sciences de Sfax, 3018 Sfax, Tunisie.

出版信息

J Biochem Mol Toxicol. 2005;19(1):12-8. doi: 10.1002/jbt.20056.

Abstract

The present study deals with the effects of Ni on the expression level of three stress proteins, namely, the cytosolic HSP72 and HSP73, and the reticulum-associated GRP94. Experiments were carried out on "Wistar'' female rats daily injected with 4 mg NiCl2 per kg body weight for 1, 3, 5, and 10 days. Another set of experiments were carried out using cell lines, derived from the monkey kidney (COS-7), and from human tumors of the lung (A549) and liver (HepG2). Cells were cultured for 4 days in the permanent presence of 100, 200, or 400 microM NiCl2. In control rats, stress proteins pattern was found to be tissue specific: two protein bands of 96 and 94 kDa were immunodetected with the anti-GRP94 antibody in kidney and liver extracts, whereas only the 96 kDa band was present in ovary extracts. HSP73 was present in kidney, liver, and ovary whereas HSP72 was only found in kidney. In kidney of nickel-treated animals, HSP73 and the 96 kDa proteins were overexpressed whereas HSP72 was strongly down regulated. No such effect was observed in liver or ovary. Similarly, in nickel-treated cell lines, HSP72 was downregulated and GRP94 (96 kDa protein) was overexpressed. HSP73 expression appeared moderately increased in A549 cells but decreased in COS-7 cells. Because long-term caloric restriction was reported to reduce free radical generation in cells, the effect of 1 month food restriction (50%) was tested in rats as a possible way to lower oxidative damages induced by Ni. No significant effect on HSP expression was observed.

摘要

本研究探讨了镍对三种应激蛋白表达水平的影响,这三种应激蛋白分别为胞质HSP72和HSP73,以及内质网相关的GRP94。实验选用“Wistar”雌性大鼠,每天每千克体重注射4毫克氯化镍,持续1、3、5和10天。另一组实验使用了来源于猴肾(COS - 7)、人肺癌(A549)和肝癌(HepG2)的细胞系。细胞在100、200或400微摩尔/升氯化镍的持续存在下培养4天。在对照大鼠中,发现应激蛋白模式具有组织特异性:用抗GRP94抗体在肾脏和肝脏提取物中免疫检测到96 kDa和94 kDa的两条蛋白带,而卵巢提取物中仅存在96 kDa的条带。HSP73存在于肾脏、肝脏和卵巢中,而HSP72仅在肾脏中发现。在镍处理动物的肾脏中,HSP73和96 kDa蛋白过度表达,而HSP72强烈下调。在肝脏或卵巢中未观察到这种效应。同样,在镍处理的细胞系中,HSP72下调,GRP94(96 kDa蛋白)过度表达。HSP73在A549细胞中的表达适度增加,但在COS - 7细胞中减少。由于据报道长期热量限制可减少细胞中的自由基产生,因此在大鼠中测试了1个月食物限制(50%)作为降低镍诱导的氧化损伤的一种可能方法。未观察到对HSP表达的显著影响。

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