吉林大学学报(医学版)

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苯丙酸诺龙对胰岛NIT-1细胞Nampt表达和胰岛素分泌的影响

乔伟1,农林琳1,冯乔1,吴雅婷1,胡婷婷1,王平1,梁瑜祯2,冯乐平1   

  1. (1. 桂林医学院生物技术学院生物技术教研室,广西 桂林 541004;2.广西医科大学第一附属医院糖尿病代谢中心,广西 南宁 530001)
  • 收稿日期:2013-12-18 出版日期:2014-07-28 发布日期:2014-07-28
  • 通讯作者: 冯乐平 E-mail:(Tel:0773-5835125,E-mail:lpfeng1226@sina.com)
  • 作者简介:乔伟(1962-),女,吉林省长春市人,高级工程师,主要从事细胞生物学和药理学方面的研究。
  • 基金资助:

    国家自然科学基金资助课题(30860116,31060161);广西壮族自治区科技厅自然科学回国基金资助课题(2010GXNSFC013016);广西壮族自治区教育厅大学生创新创业训练计划项目资助课题(桂教高教[2013]14号)

Inflnence of benzyl propionate nandrolone in Nampt expression in NIT-1 cells and insulin secretion

QIAO Wei1,NONG Lin-lin,FENG Qiao1,WU Ya-ting1,HU Ting-ting1,WANG Ping1,LIANG Yu-zhen2,FENG Le-ping1   

  1. (1. Department of Biotechnology,School of Biotechnology,Guilin Medical University,Guilin541004,China;2. Center of Diabetes Metabolism,First Affiliated Hospital,Guangxi MedicalUniversity,Naning 530021,China)
  • Received:2013-12-18 Online:2014-07-28 Published:2014-07-28

摘要:

目的:观察雄性激素苯丙酸诺龙(BPN)干预下胰岛NIT-1细胞中烟酰胺磷酸核糖转移酶(Nampt)、胰岛素受体底物-2(IRS-2)和胰岛十二指肠同源盒-1(PDX-1)蛋白表达、细胞周期和胰岛素分泌的变化,探讨高浓度葡萄糖氧化应激状态下BPN对NIT-1细胞Nampt表达和胰岛素信号分子的影响。方法:应用4种不同浓度(5.6、11.1、16.7和27.6 mmol•L-1)葡萄糖培养NIT-1细胞,以10 mg•L-1 BPN干预NIT-1细胞48 h,以未加BPN处理的相应浓度葡萄糖为对照组。应用Western blotting法检测各组细胞中Nampt、IRS-2 和 PDX-1蛋白表达水平;流式细胞术检测细胞周期;放射免疫法测定细胞胰岛素分泌水平。结果:与相应浓度葡萄糖对照组比较,各BPN处理组NIT-1细胞中Nampt、ISR-2和PDX-1蛋白表达水平增加(P<0.05或P<0.01);与相应对照组比较,在低糖(5.6 mmol•L-1)时,BPN能够明显解除细胞G0/G1期阻滞(P<0.01),在高糖(27.6 mmol•L-1)时,能够解除细胞的G2/M阻滞(P<0.01);除正常葡萄糖浓度11.1mmol•L-1组之外,各处理组细胞的胰岛素分泌水平均明显增加(P<0.01)。结论:BPN能够增加胰岛NIT-1细胞中Nampt、ISR-2和PDX-1蛋白表达水平,NIT-1细胞中Nampt表达与胰岛素信号传导途径的相关分子间可能存在密切关联,雄性激素在一定条件下能够改善胰岛细胞的胰岛素抵抗状态。

关键词: 苯丙酸诺龙, 烟酰胺磷酸核糖转移酶, 胰岛十二指肠同源盒-1, 细胞周期, 胰岛素

Abstract:

Abstract:Objective
To study the effects of benzyl propionate nandrolone (BPN) on the nicotinamide phosphoribosyl transferase (Nampt),insulin receptor substeate-2(IRS-2) and pancreatic duodenal homeobox-1(PDX-1)expressions,cell cycle changes as well as insulin secretion in pancreatic islet cell NIT-1 lines,and to explore the influence of BPN in the Nampte xpression in NIT-1 cells and insulin signaling molecules in high glucose oxidation stress.Methods The NIT-1 cells were cultured with different concentrations  (5.6,11.1,16.7, and 27.6 mmol•L-1) of glucose,then they were treated with 10 mg•L-1 BPN for 48 h with no BPN treatment as corresponding control groups. The expression levels  of Nampt,IRS-2, and PDX-1  were tested by Western blotting assay. The changes of cell cycle were determined by FCM and the cell insulin secretion levels were measured with radioimmunoassay. Results Compared with corresponding control groups,the expression levels of Nampt,IRS-2, and PDX-1 proteins in the NIT-1 cells in various BPM groups were increased (P<0.05 or P<0.01).The G0/G1 phase arrest was relieved (P<0.01) when the cells was cultured in low glucose(5.6 mmol•L-1) co ndition,and the G2/M block was remitted significantly in  high glucose  (27.6 mmol•L-1) condition (P<0.01),furthermore,the cell insulin secretion was promoted compared with control groups except 11.1 mmol•L-1 glucose group(P<0.01).Conclusion BPN can promote the expression levels of  Nampt,ISR-2 and PDX-1 proteins  in NIT-1 cells.There is close relationship between the Nampt expression in NIT-1 cells and insulin signaling pathway and BPN prevents the cells from insulin resistance.

Key words: benzyl propionate nandrolone, nicotinamide phosphoribosyl transferase, pancreatic duodenal homeobox-1, cell cycle, insulin

中图分类号: 

  • R587.1