Cui Ying-Yu, Xie Heng, Qi Kang-Biao, He Yan-Ming, Wang Jin-Fa
The State Key Laboratory for Biocontrol and The Key Laboratory of Gene Engineering of Ministry of Education, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, Guangdong Province, China.
World J Gastroenterol. 2005 Sep 14;11(34):5277-82. doi: 10.3748/wjg.v11.i34.5277.
To study the effects of Pinus massoniana bark extract (PMBE) on cell proliferation and apoptosis of human hepatoma BEL-7402 cells and to elucidate its molecular mechanism.
BEL-7402 cells were incubated with various concentrations (20-200 microg/mL) of PMBE for different periods of time. After 48 h, cell proliferation was determined by 3-(4,5-dimethyl-thiazolyl-2)-2,5-diphenyl tetrazolium bromide (MTT) assay. Apoptosis was evaluated by morphological observation, agarose gel electrophoresis, and flow cytometry analysis. Possible molecular mechanisms were primarily explored through immunohistochemical staining.
PMBE (20-200 microg/mL) significantly suppressed BEL-7402 cell proliferation in a time- and dose-dependent manner. After treatment of BEL-7402 cells with 160 microg/mL PMBE for 24, 48, or 72 h, a typical apoptotic "DNA ladder" was observed using agarose gel electrophoresis. Nuclear condensation and boundary aggregation or split, apoptotic bodies were seen by fluorescence and electron microscopy. Sub-G1 curves were displayed by flow cytometry analysis. PMBE decreased the expression levels of Bcl-2 protein in a time-dependent manner after treatment of cells with 160 microg/mL PMBE.
PMBE suppresses proliferation of BEL-7402 cells in a time- and dose-dependent manner and induces cell apoptosis by possibly downregulating the expression of the bcl-2 gene.
研究马尾松树皮提取物(PMBE)对人肝癌BEL-7402细胞增殖和凋亡的影响,并阐明其分子机制。
将BEL-7402细胞与不同浓度(20-200μg/mL)的PMBE孵育不同时间。48小时后,通过3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐(MTT)法测定细胞增殖。通过形态学观察、琼脂糖凝胶电泳和流式细胞术分析评估细胞凋亡。主要通过免疫组织化学染色初步探索可能的分子机制。
PMBE(20-200μg/mL)以时间和剂量依赖性方式显著抑制BEL-7402细胞增殖。用160μg/mL PMBE处理BEL-7402细胞24、48或72小时后,使用琼脂糖凝胶电泳观察到典型的凋亡“DNA梯带”。通过荧光和电子显微镜观察到核浓缩、边界聚集或分裂以及凋亡小体。流式细胞术分析显示亚G1峰曲线。用160μg/mL PMBE处理细胞后,PMBE以时间依赖性方式降低Bcl-2蛋白的表达水平。
PMBE以时间和剂量依赖性方式抑制BEL-7402细胞增殖,并可能通过下调bcl-2基因的表达诱导细胞凋亡。