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作 者:李莹芳[1] 夏宁[1] 冯乐平[2] 罗静思[1] 张梦霞[1] 黄荷[1] 梁瑜祯[1]
机构地区:[1]广西医科大学第一附属医院内分泌代谢科,南宁530021 [2]广西桂林医学院生物技术学院,桂林541004
出 处:《广西医科大学学报》2013年第1期1-4,共4页Journal of Guangxi Medical University
基 金:国家自然科学基金资助项目(No.30860116);广西自然科学回国基金资助项目(No.2010GXNSFC013016);博士后科研启动基金(No.02305210001)
摘 要:目的:探讨高浓度葡萄糖对胰岛β细胞胰岛素信号通路信号中胰岛素受体底物2(insulin reoeptor substance 2,Irs2)、叉头框转录因子1(forkhead transcription factors O1,FoxO1)表达的影响。方法:胰岛β细胞株NIT-1细胞培养48h后,随机分为不同葡萄糖浓度(5.6,11.1,16.7,22.5,27.6mmol/L)组,继续培养3d后终止,用MTT比色法检测细胞增殖,免疫荧光法检测细胞凋亡,放射免疫分析方法检测胰岛素水平,Real-Time PCR法检测Irs2、FoxO1mRNA变化。结果:(1)在葡萄糖浓度为11.1mmol/L时,NIT-1细胞增殖活性最强、细胞凋亡率最低,胰岛素分泌水平最高。随着葡萄糖浓度升高,细胞增殖活性和胰岛素分泌水平明显下降,细胞凋亡率逐渐增高。当葡萄糖浓度达27.6mmol/L时,细胞增殖活性和胰岛素分泌水平达最低,细胞凋亡率达到最高。(2)葡萄糖浓度为11.1mmol/L时,Irs2mRNA的转录达到最高水平,随着葡萄糖浓度的增高,Irs2mRNA的转录水平呈现逐渐减少趋势;FoxO1基因的mRNA转录水平则随着葡萄糖浓度的增高呈不断增加状态。结论:在高浓度葡萄糖条件下,葡萄糖"毒性"作用通过下调Irs2mRNA表达、增加核内的FoxO1mRNA表达以调节胰岛β细胞的功能及增殖和凋亡,分子间均有其独立的调控机制,同时又相互关联。Objective:To evaluate the effects of high concentration of glucose on insulin receptor substance 2 (Irs2) and forkhead transcription factors O1 (FoxO1) expression of pancreatic β cells. Methods: Pancreatic cell lines NIT-1 cells were cultured 48 hours, then were randomly divided into 1 to 5 groups, were cultured with 10%0 FBS DMEM medium containing glucose of 5.6, 11.1, 16.7, 22.5 and 27.6 mmol/L for 3 days. The expression of Its2 and FoxO1 mRNA in the cells was analyzed using the real-time PCR. Cell proliferation was determined by MTT, cell apoptosis was observed by immunofluorescence staining, and insulin secretion was detected by radioimmunoassay. Results: Cell proliferation and insulin secretory function in mouse NIT-1 cells were the best at the concentration of 11.1 mmol/L glucose, and cell apoptosis was the worst. With the increase of glucose concentration, cell proliferation and insulin secretion reduced obviously, the cell apoptosis increased gradually. Under the 27.6 mrnol/L glucose concentration, the pro-liferation rate and insulin lowest, the apoptosis rate secretion level were the was the best. Under the 11.1 mmol/L glucose concentration, Irs2 mRNA expression level was the best, with the increase of glu- cose concentration, it was decreased, but FoxO1 mRNA expression level was increased. Conclusion. With high concentration of glucose, glucose toxicity can re-duce Irs2 mRNA expression, increase FoxO1 mRNA expression of nuclear, regulate functional and survival of pancreatic β cells. They have independent molecular regulatory mechanism but relate each other.
分 类 号:R332[医药卫生—人体生理学]
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