吉林大学学报(医学版)

• 基础研究 •    下一篇

白附子提取物对胶质瘤细胞的增殖抑制和诱导凋亡作用及其机制

曹志友1,金宏2,田晶2, 王爽2,齐玲2,李蕴潜3   

  1. (1.吉林医药学院直属医院,吉林 吉林 132013;2.吉林医药学院病理学教研室,吉林 吉林  132013;3.吉林大学第一医院神经外科,吉林 长春 130021)
  • 收稿日期:2013-02-21 出版日期:2013-07-28 发布日期:2013-07-28
  • 通讯作者: 齐 玲 E-mail: (Tel:0432-64560027,E-mail:qiling1718@163.com)
  • 作者简介:曹志友(1967-),男,吉林省吉林市人,副教授,医学学士,主要从事抗肿瘤药物研究。
  • 基金资助:

    国家自然科学基金资助课题(81201671);吉林省教育厅科研基金资助课题(2012324,2012330)


Proliferation inhibition and inducing apoptosis of Rhizoma Typhonii extracts on glioma cells and their mechanisms


CAO Zhi-you1,JIN Hong2,TIAN Jing2,WANG Shuang2,QI Ling2,LI Yun-qian3   

  1. (1.Affiliated Hospital,Jilin Medical College,Jilin 132013,China;2.Department of Pathology,Jilin Medical College,Jilin 132013,China;3.Department of Neurosurgery,First Hospital,Jilin University,Changchun 130021,China)
  • Received:2013-02-21 Online:2013-07-28 Published:2013-07-28

摘要:

目的:研究白附子提取物对人SHG-44脑胶质瘤细胞生长的影响,初步探讨白附子对胶质瘤细胞增殖和凋亡的作用机制。方法:培养脑胶质瘤SHG-44细胞,将其分为空白对照组和8、40、200及1 000 μg•L-1白附子提取物组,MTT法检测白附子提取物对SHG-44细胞生长的影响,倒置显微镜观察细胞凋亡形态,流式细胞术分析细胞周期和细胞凋亡率,细胞免疫组织化学法检测Bcl-2与Bax蛋白表达。结果:MTT结果,与空白对照组比较,8和200 μg•L-1白附子提取物组细胞在30 min和3 h时,细胞增殖均明显受抑制,细胞增殖活性降低(P<0.05);1 000 μg•L-1白附子提取物组细胞在30 min、1 h和3 h时,细胞增殖活性均明显降低(P<0.05);不同浓度白附子提取物对胶质瘤细胞增殖抑制作用呈剂量-时间依赖性。镜下观察,与空白对照组比较,各药物组细胞均出现数量不等的凋亡小体。流式细胞术分析,部分细胞阻滞于G2/M期,细胞凋亡率随着药物浓度的增加而升高。细胞免疫组织化学检测,与空白对照组比较,200 μg•L-1白附子提取物组细胞Bcl-2蛋白表达降低(P<0.01),Bax蛋白表达增高(P<0.01)。结论:白附子提取物可抑制SHG-44细胞的增殖及诱导其发生凋亡,其作用机制与Bcl-2蛋白表达下降和Bax蛋白表达上升有关。

关键词: 白附子, 胶质瘤细胞, 细胞增殖, 细胞凋亡

Abstract:

To study the influence of Rhizoma Typhonii extracts in glioma SHG-44 cells and to explore the effects of Rhizoma Typhonii extracts on proliferation and apoptosis of glioma cells.Methods Glioma SHG-44 cells were cultured and divided into control and 8,40,200,and 1 000  μg•L-1 Rhizoma Typhonii extracts groups,and the influence of Rhizoma Typhonii extracts in proliferation of SHG-44 cells was measured by MTT assay.The morphology of apoptosis was observed with inverted microscope.The cell cycle and apoptotic rate were analyzed by flow cytometry (FCM).The expressions of Bcl-2 and Bax protein were detected by immunohistochemistry.Results Compared with control group,the poliferation of SHG-44 cells was inhibited after treated with Rhizoma Typhonii extracts at concentrations of 8 and 200 μg•L-1 for 30 min and 3 h and the proliferation activities were decreased(P<0.05);in 1 000 μg•L-1 group after treated for  30 min,1 h and 3 h,the proliferation activities were  significantly decreased (P<0.05).The proliferation inhibition of differentconcentrations of Rhizoma Typhonii extracts was time- and dose-dependent.The apoptotic bodies were found under inverted microscope in different Rhizoma Typhonii extracts groups.The FCM results showed that part of cells were arrested at G2/M phase,and the apoptotic rates were increased with the  increasing of drug concentrations.Cell immunohistochemisty showed that compared with control group the expression of Bcl-2 protein in 200 μg•L-1 Rhizoma Typhonii extracts groups was decreased(P<0.01) and the expression of Bax protein  was increased (P<0.01).Conclusion Rhizoma Typhonii extracts can inhibit the proliferation and induce apoptosis by down-regulating the Bcl-2 protein expression and up-regulating the Bax protein expression in SHG-44 cells.

Key words: Rhizoma Typhonii, glioma cells, proliferation, apoptosis

中图分类号: 

  • R739.4