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[氯离子通道蛋白3小干扰RNA抑制鼻咽癌细胞的调节性容积减小]

[ClC-3 siRNA inhibits regulatory volume decrease in nasopharyngeal carcinoma cells].

作者信息

Ye Dong, Zhang Hai-feng, Zhu Lin-yan, Wang Li-wei, Chen Li-xin

机构信息

Department of Physiology, School of Medicine, Jinan University, Guangzhou 510632, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2011 Feb;31(2):216-20.

Abstract

OBJECTIVE

To investigate the role of ClC-3 chloride channels in regulatory volume decrease (RVD) of nasopharyngeal carcinoma (NPC) CNE-2Z cells.?

METHODS

ClC-3 siRNA was transfected into CNE-2Z cells in the presence of the transfection reagent HiPerFect Reagent(TM). The transfection efficiency of ClC-3 siRNA was detected by flow cytometry. The expression of ClC-3 protein was detected by Western blotting, and the changes of cell volume in 160 mOsmol/L hypotonic solution were determined by image analysis.

RESULTS

The transfection efficiency of ClC-3 siRNA was (63.8∓3.8)% (n=3, P<0.01), and compared with the control group, ClC-3 siRNA transfection resulted in a reduction of ClC-3 expression by (60.9∓4.0)% (n=3, P<0.01). The hypotonic challege (160 mOsmol/L) caused cell swelling and induced RVD. In the control group, hypotonic solution bath for 35 min resulted in a RVD of (42.6∓2.8)% (n=20), which was significantly decreased to (10.5∓4.8)% (n=16) in ClC-3 siRNA-transfected cells, demonstrating a reduction of RVD capacity by 75.4% (P<0.01).?

CONCLUSION

The capacity of RVD is significantly reduced in CNE-2Z cells by ClC-3 chloride channel protein knock-down via ClC-3 siRNA transfection, indicating an important role of ClC-3 chloride channels in the RVD of CNE-2Z cells.

摘要

目的

探讨氯离子通道蛋白3(ClC-3)在鼻咽癌(NPC)CNE-2Z细胞调节性容积减小(RVD)中的作用。

方法

采用HiPerFect Reagent(TM)转染试剂将ClC-3小干扰RNA(siRNA)转染至CNE-2Z细胞。通过流式细胞术检测ClC-3 siRNA的转染效率。采用蛋白质免疫印迹法检测ClC-3蛋白的表达,运用图像分析技术测定细胞在160 mOsmol/L低渗溶液中的容积变化。

结果

ClC-3 siRNA的转染效率为(63.8±3.8)%(n = 3,P < 0.01),与对照组相比,ClC-3 siRNA转染使ClC-3表达降低了(60.9±4.0)%(n = 3,P < 0.01)。低渗刺激(160 mOsmol/L)导致细胞肿胀并诱导RVD。在对照组中,低渗溶液孵育35分钟导致RVD为(42.6±2.8)%(n = 20),而在ClC-3 siRNA转染的细胞中显著降低至(10.5±4.8)%(n = 16),表明RVD能力降低了75.4%(P < 0.01)。

结论

通过ClC-3 siRNA转染敲低ClC-3氯离子通道蛋白可显著降低CNE-2Z细胞的RVD能力,提示ClC-3氯离子通道在CNE-2Z细胞的RVD中起重要作用。

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