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作 者:张心桐 戚欣[1] 李静[1] ZHANG Xin-tong QI Xin LI Jing(School of Medicine and Pharmacy,Ocean University of China, Qingdao 266003, Chin)
机构地区:[1]中国海洋大学海洋药物教育部重点实验室,医药学院,山东青岛266003
出 处:《中国海洋药物》2017年第4期35-40,共6页Chinese Journal of Marine Drugs
基 金:国家自然科学基金项目(81673450)资助
摘 要:目的探讨南极土壤来源真菌的次级代谢产物HDN-1对人急性粒细胞白血病NB4细胞的增殖抑制,诱导凋亡作用及其机制。方法采用MTT法检测HDN-1对NB4细胞的增殖抑制作用;DNA结合染料Hoechst 33324染色,Western Blot实验,流式细胞仪检测细胞凋亡以及凋亡相关蛋白的变化。结果 HDN-1能显著抑制NB4细胞的增殖,并呈剂量-时间依赖性;HDN-1作用后,细胞核形态发生明显变化且流式细胞仪分析表明NB4细胞凋亡数量明显增加;HDN-1可引起Caspase-3,8,9激活,bid减少,线粒体中凋亡蛋白Bcl-2,Mcl-1的表达降低,以及γ-H2AX、Parp剪切带增加。但是NB4细胞中融合蛋白PML-RARα的表达不能被HDN-1所抑制。结论 HDN-1诱导凋亡是通过Caspase依赖的线粒体途径和死亡受体途径共同介导的,PML-RARα不是Hsp90的客户蛋白,其诱导凋亡机制可能是通过抑制Hsp90的其他蛋白表达进行的。Objective To investigate the mechanisms of proliferation inhibition and inducing apoptosis of human acute promyelocytic leukimic cells NB by HDN-1, a secondary metabolite of Antarctic soil fun- gi. Methods MTT assay was applied to examine the effect of HDN-1 on the proliferation inhibition of NIM cells. Hoechst 33324 staining, Western Blot and FCM were used to detect the apoptosis of NB4 cells. Results HDN-1 could inhibit the proliferation and induce apoptosis in NB4 cells in time- and dose- dependent manners. Typical morphological changes were observed under the treatment of HDN-1. Western Blot showed cleavage of the caspase-3,8, 9 zymogen protein and an 89kDa subunit cleavage product of ADP-ribose Parp after treatment of HDN-1. Moreover, Western Blot also revealed that the expression of anti-apoptotic protein bcl-2 and Mcl-1 was up-regulated, and PML-RARα could not de- grade after treatment of HDN-1. FCM figures also showed the effect of HDN-1 on the proliferation in- hibition of NPA cells. Conclusion All these results suggested that HDN-1 induced apoptosis of NB4 cells by caspase-dependent pathway and death receptor pathway. PML-RARa wasn't client protein of Hsp90, so the mechanism of HDN-1-induced apoptotic could be inhibition other client protein of Hsp90.
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