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[糖基磷脂酰肌醇特异性磷脂酶D基因表达对K562细胞补体杀伤敏感性的影响]

[Effect of the expression of glycosylphosphatidylinositol-specific phospholipase D gene on K562 cell sensitivity to complement killing].

作者信息

Wang Yi-dan, Tang Jian-hua, Yang Zhi-ying, Yu Hong, Xiang Xin-ying

机构信息

Department of Biochemistry, Insitute of Biological Scienee and Technology, Central South University, Changsha 410078, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2004 Dec;29(6):654-7.

Abstract

OBJECTIVE

To detect the release of glycosylphosphatidylinositol (GPI) anchored CD55 and CD59, and the effect of complement dependent cytotoxicity on K562 cell with expression of GPI-PLD by glucose or insulin.

METHODS

CD55 and CD59 were detected by Western blotting; GPI-PLD activities were analyzed quantitatively; and complement dependent cytotoxicity (CDC) effects were observed by staining of trypan blue.

RESULTS

After being induced by insulin or glucose for 24 h and 48 h, GPI-PLD activities and rate of CDC killing in the insulin, insulin + glucose groups significantly increased. At 24 h after the inducement, CD55 was found in the membrane proteins in the control, glucose and insulin groups and CD59 in membrane proteins in the control, glucose group, and medium supernatants of insulin, glucose + insulin groups. Both CD55 and CD59 were found in membrane proteins in control group, and medium supernatants of glucose, insulin, glucose + insulin group at 48 h after the inducement.

CONCLUSION

Treatment with insulin resulted in the obvious increase of GPI-PLD activity in K562 cell, which led to releasing of GPI anchored CD55 and CD59 into medium, and increased sensitivity of these cells to CDC killing.

摘要

目的

检测糖基磷脂酰肌醇(GPI)锚定的CD55和CD59的释放情况,以及葡萄糖或胰岛素对表达GPI-PLD的K562细胞补体依赖性细胞毒性的影响。

方法

采用蛋白质免疫印迹法检测CD55和CD59;定量分析GPI-PLD活性;通过台盼蓝染色观察补体依赖性细胞毒性(CDC)效应。

结果

胰岛素或葡萄糖诱导24小时和48小时后,胰岛素组、胰岛素+葡萄糖组的GPI-PLD活性和CDC杀伤率显著增加。诱导24小时后,对照组、葡萄糖组和胰岛素组的膜蛋白中可检测到CD55,对照组、葡萄糖组以及胰岛素组、葡萄糖+胰岛素组的培养基上清中可检测到CD59。诱导48小时后,对照组、葡萄糖组、胰岛素组、葡萄糖+胰岛素组的膜蛋白及培养基上清中均可检测到CD55和CD59。

结论

胰岛素处理可使K562细胞中GPI-PLD活性明显增加,导致GPI锚定的CD55和CD59释放到培养基中,并增加这些细胞对CDC杀伤的敏感性。

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