吉林大学学报(医学版)

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5-硝基-2-(3-苯丙胺)苯甲酸对人脑胶质瘤SHG-44细胞增殖的作用及其机制

田晶1,齐玲2,金宏3, 陈雪3, 王春艳1   


  1. (1.吉林医药学院生理学教研室,吉林 吉林 132013;2.吉林医药学院病理学教研室,吉林 吉林 132013;3.吉林医药学院实验中心,吉林 吉林 132013)
  • 收稿日期:2013-05-24 出版日期:2014-01-28 发布日期:2014-01-28
  • 通讯作者: 齐 玲 E-mail:(Tel:0432-64560027,E-mail:qiling1718@163.com)
  • 作者简介:田 晶(1973-),女,吉林省吉林市人,副教授,医学硕士,主要从事细胞增殖研究。
  • 基金资助:

    国家自然科学基金资助课题((81201671);吉林省教育厅基金资助课题(2011281,2012330)

Effect of NPPB on proliferation of human glioma SHG-44 cells and its mechamism

TIAN Jing1,QI Ling2,JIN Hong3,CHEN Xue3,WANG Chun-yan1   

  1. (1.   Department of Physiology,Jilin Medical College,Jilin 132013,China;2. Department of Pathology,Jilin Medical College,Jilin 132013,China;3. Experimental Center,Jilin Medical College,Jilin 132013,China)
  • Received:2013-05-24 Online:2014-01-28 Published:2014-01-28

摘要:

目的:探讨氯通道阻断剂5-硝基-2-(3-苯丙胺)苯甲酸(NPPB)对人脑胶质瘤SHG-44细胞生长的影响,初步阐明NPPB抑制胶质瘤细胞增殖和诱导细胞凋亡的可能机制。方法:培养人脑胶质瘤SHG-44细胞,将其分为空白对照组和50、100及200  μmol•L-1 NPPB组,MTT法检测各组SHG-44细胞的增殖活性,细胞分析仪分析细胞周期变化及凋亡率。结果:MTT检测,与空白对照组比较,50   μmol•L-1 NPPB 组在48 h时细胞增殖活性降低(P<0.05),200  μmol•L-1 NPPB组3 h时细胞增殖活性增高(P<0.05),100和200   μmol•L-1 NPPB组24和48 h时细胞增殖活性明显降低(P<0.01)。细胞周期检测,与空白对照组比较,50  μmol•L-1 NPPB组G1期细胞百分数明显减少,G2/M期细胞百分数明显增多(P<0.01),100和200  μmol•L-1 NPPB组细胞增殖停滞在G1期(P<0.01)。细胞凋亡检测,与空白对照组比较,100和200  μmol•L-1 NPPB组细胞凋亡率明显升高,分别达到24.64%和41.85%(P<0.01)。结论:高浓度NPPB可以抑制人脑胶质瘤SHG-44细胞的增殖并诱导其凋亡,提示氯通道在人脑胶质瘤SHG-44细胞的增殖与凋亡中起一定的作用。

关键词: 氯通道, 胶质瘤, 细胞增殖, 细胞凋亡

Abstract:

To explore the effect of [5-nitro-2-(3-phenylpropylamino)-benzoic acid]NPPB,a chloride channel blocker,on the growth of human glioma SHG-44 cells and to clarify  the potential mechanism of proliferation inhibition and apoptosis induction of NPPB on SHG-44 cells.Methods The glioma SHG-44 cells were cultured and divided into control and 50,100 and 200   μmol•L-1 NPPB groups,and the influence of NPPB in proliferation of SHG-44 cells was measured by MTT assay.The cell cycle and apoptotic rate were analyzed by Cell Analysis Machine.Results Compared with control group,the proliferation of SHG-44 cells was inhibited after treated with 50   μmol•L-1 NPPB for 48 h (P<0.05),the proliferation of SHG-44 cells was improved after treated with 200   μmol•L-1 NPPB for 3 h (P<0.05) and the proliferation of SHG-44 cells were inhibited significantly after treated with 100 and 200   μmol•L-1 NPPB for 24 and 48 h (P<0.01).The detection  results of cell cycle showed that compared with control group,the percentage  of SHG-44 cells  in G1 phase was decreased and the percentage of SHG-44 cells in G2/M phase was increased(P<0.01) in 50   μmol•L-1 NPPB group 24 h after treatment;Part of SHG-44  cells was arrested in G1 phase in 100 and 200   μmol•L-1 NPPB groups 24 h after treatment(P<0.01).The detection  results of apoptosis  showed that the apoptotic rates of SHG-44 cells were increased to 24.64% and 41.85% after treated with 100 and 200   μmol•L-1 NPPB for 24 h, respectively,compared with control group (P<0.01).Conclusion High doses of NPPB can inhibit the proliferation and induce apoptosis of SHG-44 glioma cells,which indicates that chloride channels may play essential roles in the proliferation and apoptosis of human glioma SHG-44 cells.

Key words: chloride channel, glioma, cell proliferation, apoptosis

中图分类号: 

  • R739.4