Zhou Na, Yang Li, Tang Jia-Wei, Li Xiao-Mei
Renal Division, Department of Medicine, First Hospital and Institute of Nephrology, Peking University, Beijing 100034, China.
Zhongguo Zhong Yao Za Zhi. 2008 Oct;33(19):2222-6.
The purpose of this study was to investigate the effects of exogenous epidermal growth factor (EGF) on the growth inhibition of renal proximal tubular epithelial cell induced by AA-I.
Cultured human renal proximal tubular epithelial cell line HK-2 was used as the subject. The changes of the survived HK-2 cells were observed and compared among control, AA-I stimulation, pre-EGF, together-EGF and post-EGF groups. In the study, cellular morphologic assessments were performed with a phase-contrast inverted microscope. Cell counting after stained with 0.04% trypan blue was adopted to analyze cell proliferation. Cell cycle was assessed by flow cytometry.
Number of the survived cells stimulated by AA-I for 12, 24, 48 hours decreased gradually in a dose and time dependent manner. At 24, 48 hours, the survived cells showed a significant disturbance in the cell cycle procedure, which was characterized as decreased percentage of cells in G0/G1 phase, significant increased percentage of cells in G2/M phases. Exogenous EGF (20 microg L(-1)) could significantly promote the proliferation of HK-2 cells, which shown a increased cell number, accompanied down-regulated cells in G0/G1 phase, increased cells in S and G2/M phase. Compared with AA-I groups, it failed to improve the inhibitory effect on cell proliferation and abnormal cell cycle procedure by AA-I, no matter EGF was added in before, at same time or after AA-I stimulation.
AA-I (10 g L(-1)) has remarkable growth inhibition effects on survived RTEC, and can induce a blockage of G2/M phase in the cell cycle procedure. Exogenous EGF (20 microg L(-1)) promote the proliferation in normal cultured HK-2 cell. EGF treatment could not improve the proliferation inhibitory effect induced by AA-I, no matter adding EGF to cultures before, together with AA-I or after AA-I stimulation.
本研究旨在探讨外源性表皮生长因子(EGF)对AA-I诱导的肾近端小管上皮细胞生长抑制的影响。
以培养的人肾近端小管上皮细胞系HK-2为研究对象。观察并比较对照组、AA-I刺激组、预EGF组、共EGF组和后EGF组中存活的HK-2细胞的变化。研究中,使用相差倒置显微镜进行细胞形态学评估。采用0.04%台盼蓝染色后进行细胞计数以分析细胞增殖。通过流式细胞术评估细胞周期。
AA-I刺激12、24、48小时后存活细胞数量呈剂量和时间依赖性逐渐减少。在24、48小时时,存活细胞的细胞周期进程出现明显紊乱,表现为G0/G1期细胞百分比降低,G2/M期细胞百分比显著增加。外源性EGF(20μg L(-1))可显著促进HK-2细胞增殖,表现为细胞数量增加,同时G0/G1期细胞下调,S期和G2/M期细胞增加。与AA-I组相比,无论在AA-I刺激前、同时还是刺激后添加EGF,均未能改善AA-I对细胞增殖和异常细胞周期进程的抑制作用。
AA-I(10 g L(-1))对存活的肾小管上皮细胞具有显著的生长抑制作用,并可诱导细胞周期进程中G2/M期阻滞。外源性EGF(20μg L(-1))可促进正常培养的HK-2细胞增殖。无论在培养前、与AA-I同时还是在AA-I刺激后添加EGF,EGF处理均不能改善AA-I诱导的增殖抑制作用。