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首页> 外文期刊>Annals of Cancer Research and Therapy >MSCs modifies the proliferation of leukemia MOLT-4 cells and induces their apoptosis through up-regulating Bax, caspase-3, and-8, and down-regulating Bcl-2 expression
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MSCs modifies the proliferation of leukemia MOLT-4 cells and induces their apoptosis through up-regulating Bax, caspase-3, and-8, and down-regulating Bcl-2 expression

机译:MSCS改变白血病Molt-4细胞的增殖,并通过上调节Bax,Caspase-3和-8和下调Bcl-2表达诱导它们的细胞凋亡

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Currently, it has been suggested that human mesenchymal stem cells (MSCs), a well-known multipotent stem cells, could modify the biological process in leukemia cells. Therefore, we evaluated human MSCs’ possible effects on apoptosis and proliferation of acute lymphoblastic leukemia (ALL) MOLT-4 cells. Accordingly, MOLT-4 cells were co-cultured with MSCs. Then, 24, 48, and 72 hours after treatment, the apoptosis percentages of co-cultured MOLT-4 cell apoptosis was estimated using flow cytometry analysis. Also, cells proliferation rates were measured by MTT assay after 24, 48, and 72 hours of treatment. Finally, the expression ratio of candidate genes, including Bax, Bcl-2, and caspase-3, and -8, were evaluated in MOLT-4 cells co-cultured with MSCs. Based on results, MSCs stimulated the apoptosis of MOLT-4 cells after 48 and 72 hours but not 24 hours of treatment compared with the control group (MOLT-4 cells). Also, MSCs induced robust a reduction in MOLT-4 cell proliferation rate compared with the control group. On the other hand, Real-Time PCR results indicated a decrease in Bcl-2 expression, and conversely a promotion in Bax, and caspase-3, and -8 expression at mRNA levels. In sum, results signified that MSCs could exert anti-leukemic effects on leukemia MOLT-4 cells through promoting Bax/Bcl-2 ration concomitant with up-regulating caspases expression.
机译:目前,已经表明人间充质干细胞(MSCs),一种众所周知的多能干细胞,可以改变白血病细胞中的生物过程。因此,我们评估了人体MSCS对急性淋巴细胞白血病(全)MOLT-4细胞的凋亡和增殖的影响。因此,用MSCs共培养MOLT-4细胞。然后,治疗后24,48和72小时,使用流式细胞仪分析估计共培养蜕皮-4细胞凋亡的凋亡百分比。此外,通过在24,48和72小时后通过MTT测定测量细胞增殖速率。最后,在用MSC共同培养的Molt-4细胞中评估候选基因的表达比,包括Bax,Bcl-2和Caspase-3和-8。基于结果,MSCs刺激了48和72小时后莫尔特-4细胞的凋亡,但与对照组(Molt-4细胞)相比,没有24小时治疗。此外,与对照组相比,MSCs诱导摩尔-4细胞增殖速率的稳健降低。另一方面,实时PCR结果表明Bcl-2表达的降低,并相反于BAX和Caspase-3的促进和MRNA水平的-8表达。总之,结果表示MSCs可以通过促进BAX / BCL-2的伴随与Up-Cancated Caspases表达伴随的Bax / Bcl-2配量对白血病Molt-4细胞产生抗白血病作用。

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