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改性阿拉伯木聚糖米糠(MGN-3/生物麸皮)使人类T细胞白血病细胞对死亡受体(CD95)诱导的凋亡敏感。

Modified arabinoxylan rice bran (MGN-3/Biobran) sensitizes human T cell leukemia cells to death receptor (CD95)-induced apoptosis.

作者信息

Ghoneum Mamdooh, Gollapudi Sastry

机构信息

Department of Otolaryngology, Drew University of Medicine and Science, 1621 E. 120th Street, Los Angeles, CA 90059, USA.

出版信息

Cancer Lett. 2003 Nov 10;201(1):41-9. doi: 10.1016/s0304-3835(03)00458-0.

Abstract

MGN-3, an arabinoxylan extracted from rice bran that is treated enzymatically with an extract from Shiitaki mushrooms, is an effective biological response modifier that increases NK cell activity, and potentiates the activity of conventional chemotherapeutic agents. In this study, we investigated the effect of MGN-3 on death receptor-induced apoptosis in the human leukemic HUT 78 cell line. HUT 78 cells were pre-treated with MGN-3, and then were incubated with the agonistic antibody against death receptor (Fas, CD95). Apoptosis was determined by the propidium iodide technique using FACScan. Activation of caspase 3, caspase 8, and caspase 9 was determined by flow cytometry. Mitochondrial membrane potential was measured with DIOC(6) dye using FACScan. Expression of CD95 and Bcl-2 were measured by flow cytometry. In a dose-dependent manner, MGN-3 enhanced anti-CD95 antibody-induced apoptosis. Increased cell death was correlated with increased depolarization of mitochondrial membrane potential and increased activation of caspase 3, caspase 8, and caspase 9. MGN-3 treatment had no effect on the level of expression of CD95, but it caused down regulation of Bcl-2 expression. These results suggest that MGN-3 increases the susceptibility of cancer cells to undergo apoptosis mediated by death ligands, which may be relevant for anti-cancer activities.

摘要

MGN-3是一种从米糠中提取的阿拉伯木聚糖,经香菇提取物酶处理后,是一种有效的生物反应调节剂,可增加自然杀伤细胞活性,并增强传统化疗药物的活性。在本研究中,我们研究了MGN-3对人白血病HUT 78细胞系中死亡受体诱导的细胞凋亡的影响。HUT 78细胞先用MGN-3预处理,然后与抗死亡受体(Fas,CD95)的激动性抗体孵育。使用FACScan通过碘化丙啶技术测定细胞凋亡。通过流式细胞术测定caspase 3、caspase 8和caspase 9的激活情况。使用FACScan用DIOC(6)染料测量线粒体膜电位。通过流式细胞术测量CD95和Bcl-2的表达。MGN-3以剂量依赖的方式增强抗CD95抗体诱导的细胞凋亡。细胞死亡增加与线粒体膜电位去极化增加以及caspase 3、caspase 8和caspase 9的激活增加相关。MGN-3处理对CD95的表达水平没有影响,但它导致Bcl-2表达下调。这些结果表明,MGN-3增加了癌细胞对死亡配体介导的细胞凋亡的敏感性,这可能与抗癌活性有关。

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