单磷酸环磷酸腺苷通过激活人类白血病 HL-60 细胞中的蛋白激酶 A 抑制熊果酸诱导的细胞凋亡。

B M Choi, R Park, H O Pae, J C Yoo, Y C Kim, C D Jun, B H Jung, G S Oh, H S So, Y M Kim, H T Chung
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引用次数: 37

摘要

本研究旨在探讨 cAMP 对熊果酸诱导的 HL-60 细胞凋亡的影响。熊果酸以剂量依赖的方式降低了细胞的活力,凋亡过程表现为琼脂糖凝胶电泳中梯形DNA片段和DAPI-磺胺101染色中的细胞核分割。添加 cAMP 升高剂(包括 DB-cAMP、CPT-cAMP、8-Br-cAMP 和福斯克林)可明显抑制熊果酸诱导的细胞凋亡。包括 H89 和 KT5720 在内的 cAMP 依赖性蛋白激酶抑制剂完全抑制了 cAMP 介导的拯救 HL-60 细胞免于熊果酸诱导的细胞凋亡的作用,这一事实进一步证明了上述结果。此外,二甲基亚砜和维甲酸等细胞分化剂也不影响熊果酸诱导的 HL-60 细胞凋亡。这些结果表明,cAMP 依赖性激活蛋白激酶 A 的信号通路可能会影响肿瘤细胞对熊果酸的反应性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cyclic adenosine monophosphate inhibits ursolic acid-induced apoptosis via activation of protein kinase A in human leukaemic HL-60 cells.

This study was designed to investigate the effect of cAMP on ursolic acid-induced apoptosis of HL-60 cells. Ursolic acid decreased the viability of the cells in a dose-dependent manner, which was revealed as an apototic process characterized by ladder-pattern DNA fragmentation in agarose gel electrophoresis and segmented nuclei in DAPI-sulpharhodamin 101 staining. Ursolic acid-induced apoptosis of the cells was markedly inhibited by the addition of cAMP-elevating agents including DB-cAMP, CPT-cAMP, 8-Br-cAMP and forskolin. These results were further evidenced by the fact that inhibitors of cAMP-dependent protein kinase including H89 and KT5720 completely inhibited the cAMP-mediated rescue of HL-60 cells from ursolic acid-induced apoptosis. In addition, differentiating agents of the cells such as dimethyl sulfoxide and retinoic acid did not affect the ursolic acid-induced apoptosis of HL-60 cells. These results suggest that signaling pathway of cAMP-dependent activation of protein kinase A may affect the responsiveness of tumor cells upon ursolic acid.

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