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中国临床药理学与治疗学 ›› 2007, Vol. 12 ›› Issue (5): 566-570.

• 基础研究 • 上一篇    下一篇

苦参碱诱导RPMI8226 细胞凋亡及其对Bcl-2 、增殖细胞核抗原蛋白表达的影响

章圣辉1, 俞康2, 吴建波1, 韩义香1, 熊术道1, 谭映霞1   

  1. 1温州医学院附属第一医院医学科学研究所, 2血液科,温州 325000,浙江
  • 收稿日期:2007-02-09 修回日期:2007-04-04 发布日期:2020-10-29
  • 作者简介:章圣辉,男,主管技师,研究方向:免疫学及细胞生物学。Tel:0577-86550276 E-mail:shenghuizhang1@126.com

Induction of apoptosis by matrine in RPMI8226 cells and its effect on Bcl-2 and proliferating cell nuclear antigen

ZHANG Sheng-hui1, YU Kang2, WU Jian-bo1, HAN Yi-xiang1, XIONG Shu-dao1, TAN Ying-xia1   

  1. 1Institute of Medical Sciences, 2Department of Hematology, the First Affiliated Hospital of Wenzhou Medical College, Wenzhou 325000, Zhejiang, China
  • Received:2007-02-09 Revised:2007-04-04 Published:2020-10-29

摘要: 目的: 研究苦参碱是否具有诱导RPMI8226细胞凋亡的生物学活性,探讨苦参碱对RPMI8226细胞Bcl-2及增殖细胞核抗原(PCNA)表达水平的影响及其作用的分子机制。方法: CCK-8法检测一定浓度的苦参碱对RPMI8226细胞的体外增殖抑制作用;AnnexinV PI 染色法检测细胞凋亡;PI单染色法检测细胞周期改变;同时应用流式细胞术检测Bcl-2及PCNA蛋白表达的变化。结果: 苦参碱对RPMI8226细胞生长具有明显的抑制作用,呈量效和时效关系;苦参碱能诱导RPMI8226细胞凋亡,呈量效关系;细胞周期分析,G0G1期细胞相对增多、S期相对减少、G2M期无明显变化。苦参碱处理组RPMI8226 细胞中Bcl-2及PCNA蛋白的表达跟未加药组相比阳性表达率均降低。结论: 苦参碱对RPMI8226细胞生长具有明显抑制作用,其作用主要通过诱导RPMI8226细胞产生细胞周期阻滞和凋亡,降低PCNA的表达。苦参碱诱导RPMI8226细胞凋亡过程中,Bcl-2 蛋白表达下调对调控细胞凋亡有重要作用。

关键词: 苦参碱, RPMI8226 细胞, 细胞凋亡, 细胞周期, Bcl-2

Abstract: AIM: To explore whether the apoptosis was induced by matrine and its effect on the expression of Bcl-2 and proliferating cell nuclear antigen (PCNA) in human mutiple myeloma cell line RPMI8226 cells. METHODS: RPMI8226 cells were incubated with indicated concentrations of matrine. The growth of RPMI8226 cells was observed by CCK-8 colorimetric assay, and apoptosis rates were detected by flow cytometry using Annexin V-FITC PI staining. The cell cycles were analyzed by PI staining. Flow cytometry was used to detect the expression of Bcl-2 and PCNA. RESULTS: RPMI8226 cells viability in presence of matrine decreased markedly in a dose and time-dependent manner. The apoptosis could be induced by matrine and its level increased following the augmentation of the drug concentration. After treated by matrine for 48 h, a concentration-dependent increase of cells in G0 G1 phase and a decrease in S phase were detected, but there was no obvious change at G2 M phase. Treatment of RPMI8226 cells with matrine for 48 h provoked a decrease in the level of expression of Bcl-2 and PCNA. CONCLUSION: Matrine can significantly inhibit the growth of RPMI8226 cells, its function is performed by inducing apoptosis and arresting cell cycles. Bcl-2down-expression may probably function as an important regulator in the process of apoptosis induced by matrine.

Key words: matrine, RPMI8226 cell, apoptosis, cell cycle, Bcl-2

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