首页> 外文期刊>General Pharmacology >Activation of caspase cascades in Korean mistletoe (Viscum album var. coloratum) lectin-II-induced apoptosis of human myeloleukemic U937 cells.
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Activation of caspase cascades in Korean mistletoe (Viscum album var. coloratum) lectin-II-induced apoptosis of human myeloleukemic U937 cells.

机译:caspase级联的激活在韩国槲寄生(Viscum Album var。coloratum)凝集素II诱导的人类骨髓性U937细胞凋亡中。

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摘要

Mistletoe lectins are of high biological activity and exert cytotoxic effects. We have previously shown that Korean mistletoe, Viscum album var. coloratum, lectin-II specifically induces apoptotic cell death in cancer cells, not normal lymphocytes. The destructive mechanism by mistletoe lectins on tumor cells was mediated by activation of c-JUN N-terminal kinase (JNK)/stress-activated protein kinase. Herein, we investigated the involvement of caspase cascade and its proteolytic cleavage effects on biosubstrates of human myeloleukemic U937 cells by D-galactoside and N-acetyl-galactosamine-specific Korean mistletoe lectin-II. Mistletoe lectin-II induced ladder pattern DNA fragmentation and activation of caspase-3, -8, and -9 of U937 cells, but not caspase-1 protease, in a time- and dose-dependent manner. Consistent with catalytic activation of protease, both poly(ADP-ribose) polymerase (PARP) and protein kinase C-delta (PKC-delta) are also cleaved in mistletoe lectin-II-treated U937 cells. An inhibitor of caspase-3-like protease, DEVD-CHO peptide, significantly inhibited mistletoe lectin-II-induced apoptosis, PARP cleavage, and fragmentation of DNA. These results provide the evidence that Korean mistletoe lectin-II induces apoptotic death of U937 cells via activation of caspase cascades.
机译:槲寄生凝集素具有很高的生物活性,并具有细胞毒性作用。先前我们显示过朝鲜槲寄生,Viscum专辑var。色氨酸,凝集素-II特异性诱导癌细胞而非正常淋巴细胞的凋亡。槲寄生凝集素对肿瘤细胞的破坏机制是通过激活c-JUN N末端激酶(JNK)/应激激活的蛋白激酶介导的。在这里,我们调查了半胱氨酸天冬氨酸蛋白酶级联的参与及其对D-半乳糖苷和N-乙酰-半乳糖胺特异性韩国槲寄生凝集素-II对人骨髓白血病U937细胞生物底物的蛋白水解切割作用。槲寄生凝集素II以时间和剂量依赖性方式诱导U937细胞的caspase-3,-8和-9而不是caspase-1蛋白酶的梯形DNA断裂和活化。与蛋白酶的催化活化一致,聚(ADP-核糖)聚合酶(PARP)和蛋白激酶C-δ(PKC-δ)也在槲寄生凝集素-II处理的U937细胞中被裂解。 caspase-3样蛋白酶的抑制剂DEVD-CHO肽显着抑制槲寄生凝集素II诱导的细胞凋亡,PARP裂解和DNA断裂。这些结果提供了证据,证明韩国槲寄生凝集素II通过激活半胱天冬酶级联反应诱导U937细胞凋亡性死亡。

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