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Costunolide Triggers Apoptosis in Human Leukemia U937 Cells by Depleting Intracellular Thiols

机译:Costunolide通过消耗细胞内硫醇来触发人白血病U937细胞凋亡。

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摘要

We have previously demonstrated that costunolide, a biologically active compound that was isolated from the stem bark of Magnolia sieboldii, induced apoptosis in human cancer cells. In the present study, we investigated the underlying mechanisms and suggest that costunolide induces apoptosis in human promonocytic leukemia U937 cells by depleting the intracellular thiols. Costunolide treatment rapidly depleted the intracellular reduced glutathione (GSH) and protein thiols, and this preceded the occurrence of apoptosis. Pretreatment with sulfhydryl compounds such as GSH, N‐acetyl‐L‐cysteine, dithiothreitol and 2‐mercaptoethanol almost completely blocked the costunolide‐induced apoptosis, highlighting the significance of the intracellular thiol level in the process. Furthermore, overexpression of Bcl‐2 also significantly attenuated the effects of costunolide. The apoptosis‐inducing activity of costunolide is likely to depend on the exomethylene moiety because derivatives in which this group was reduced, such as dihydrocostunolide and saussurea lactone, did not deplete the cellular thiols and showed no apoptotic activity. Taken together, the present study demonstrates that the costunolide‐induced apoptosis depends on intracellular thiols contents, which are modulated by Bcl‐2.
机译:我们以前已经证明,木香酚是一种从木兰茎皮中分离出来的生物活性化合物,可诱导人癌细胞凋亡。在本研究中,我们调查了潜在的机制,并建议,木香酚内酯通过消耗细胞内硫醇来诱导人单核细胞白血病U937细胞凋亡。 Costunolide治疗迅速耗尽了细胞内还原型谷胱甘肽(GSH)和蛋白质硫醇,这是在细胞凋亡发生之前。用巯基化合物如GSH,N-乙酰基-L-半胱氨酸,二硫苏糖醇和2-巯基乙醇进行的预处理几乎完全阻断了木香酚诱导的细胞凋亡,从而突出了细胞内硫醇水平在此过程中的重要性。此外,Bcl-2的过表达也显着减弱了木香酚的作用。木香酚内酯的细胞凋亡诱导活性可能取决于外亚甲基部分,因为其中该基团被还原的衍生物,如二氢木香酚内酯和雪莲内酯,没有耗尽细胞硫醇,也没有凋亡活性。综上所述,本研究表明,木香酚内酯诱导的细胞凋亡取决于细胞内硫醇含量,该含量受Bcl-2调节。

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