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

机译:葡萄糖调节蛋白78在链脲佐菌素影响的胰腺β细胞不同相中的改变表达

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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)应激介导的凋亡在胰腺β细胞破坏中发挥着重要作用,有助于1型糖尿病的发育。伴侣分子,葡萄糖调节的蛋白质78(GRP78)需要在有毒损伤期间维持ER功能。在这项研究中,我们研究了链脲佐菌素(STZ) - 受理β细胞的不同阶段GRP78表达的变化,探讨了GRP78与β细胞对ER应激的响应之间的关系。用STZ对不同时间段和STZ诱导的不同时间点的糖尿病BALB / C小鼠处理的胰岛素瘤细胞系(NIT-1)作为模型系统。通过免疫印迹通过实时聚合酶链反应及其蛋白质检测GRP78和C / EBP同源蛋白(Chec)mRNA的水平。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到STZ处理的非糖尿病小鼠中GRP78蛋白的变化。 GRP78表达在早期阶段显着增加,但在受影响的β细胞的后期阶段下降,而剁碎诱导,并随着GRP78的降低而发生凋亡。有趣的是,与对照相比,STZ治疗的非糖尿病小鼠的GRP78蛋白质增加。从结果中,我们可以得出结论,GRP78可能有助于β细胞对ER压力的响应,并且应在改善糖尿病中支付给GRP78的更多关注。

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