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The altered expression of glucose-regulated proteins 78 in different phase of streptozotocin-affected pancreatic beta-cells

机译:链脲佐菌素感染的胰腺β细胞不同阶段葡萄糖调节蛋白78表达的改变

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摘要

Endoplasmic reticulum (ER) stress-mediated apoptosis plays an important role in the destruction of pancreatic beta-cells and contributes to the development of type 1 diabetes. The chaperone molecule, glucose-regulated proteins 78 (Grp78), is required to maintain ER function during toxic insults. In this study, we investigated the changes of Grp78 expression in different phases of streptozotocin (STZ)-affected beta-cells to explore the relationship between Grp78 and the response of beta-cells to ER stress. An insulinoma cell line (NIT-1) treated with STZ for different time periods and STZ-induced diabetic Balb/C mice at different time points were used as the model system. The level of Grp78 and C/EBP homologous protein (CHOP) mRNA were detected by real-time polymerase chain reaction and their protein by immunoblot. Apoptosis and necrosis was measured by flow cytometry. In addition, the changes of Grp78 protein in STZ-treated nondiabetic mice were also detected by immunoblot. Grp78 expression significantly increased in the early phase but decreased in the later phase of affected beta-cells, while CHOP was induced and apoptosis occurred along with the decrease of Grp78. Interestingly, the Grp78 protein of STZ-treated nondiabetic mice increased stably compared with that of the control. From the results, we can conclude that Grp78 may contribute to the response of beta-cells to ER stress, and more attention should be paid to Grp78 in the improvement of diabetes.
机译:内质网(ER)应激介导的细胞凋亡在胰腺β细胞的破坏中起重要作用,并有助于1型糖尿病的发展。伴侣分子,葡萄糖调节蛋白78(Grp78),是维持中毒时内质网功能所必需的。在这项研究中,我们调查了受链脲佐菌素(STZ)影响的β细胞在不同阶段的Grp78表达的变化,以探讨Grp78与β细胞对内质网应激反应之间的关系。以STZ处理不同时间段的胰岛素瘤细胞系(NIT-1)和STZ诱导的糖尿病Balb / C小鼠在不同时间点作为模型系统。通过实时聚合酶链反应检测Grp78和C / EBP同源蛋白(CHOP)mRNA的水平,并通过免疫印迹检测其蛋白。通过流式细胞术测量细胞凋亡和坏死。此外,还通过免疫印迹检测了STZ治疗的非糖尿病小鼠中Grp78蛋白的变化。 Grp78表达在受影响的β细胞的早期显着增加,而在晚期减少,而CHOP被诱导并且凋亡随Grp78的减少而发生。有趣的是,与对照组相比,经STZ治疗的非糖尿病小鼠的Grp78蛋白稳定增加。从结果中我们可以得出结论,Grp78可能有助于β细胞对内质网应激的反应,在改善糖尿病方面应更加注意Grp78。

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