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骨髓瘤细胞中阿霉素诱导的ATP变化与自噬的关系
引用本文:余芳,陈协群,陈娟娟,黄晓梅.骨髓瘤细胞中阿霉素诱导的ATP变化与自噬的关系[J].生物磁学,2011(6):1030-1032.
作者姓名:余芳  陈协群  陈娟娟  黄晓梅
作者单位:第四军医大学西京医院血液内科,陕西西安710032
基金项目:国家自然科学基金(NO.30871089)
摘    要:目的:检测用阿霉素(doxorubicin DOXO)处理的骨髓瘤细胞株NCI-H929中ATP与自噬表达水平的变化,探讨两者之间的关联。方法:分别以DOXO 2umol/l 24h、DOXO 2umol/l联用自噬抑制剂3MA 10mmol/l 24h处理H-929细胞后,采用MTT法检测细胞存活率;ATP生物发光法检测ATP表达量;Western Blot检测靶细胞自噬标志分子LC3蛋白的表达。结果:各组相对未处理组存活率分别为54%、35%;相对未处理组%ATP分别为400%、150%;DOXO 24h LC3表达显著上调。结论:经DOXO处理H-929细胞系自噬形成,进而ATP上升以保护细胞。

关 键 词:阿霉素  骨髓瘤  三磷酸腺苷  自噬  NCI-H929细胞  LC3

Relationship between ATP and Autophagy in Myeloma Cell Lines NCI-H929 Induced by Doxorubicin
YU Fang,CHEN Xie-qun,CHEN Juan-juan,HUANG Xiao-mei.Relationship between ATP and Autophagy in Myeloma Cell Lines NCI-H929 Induced by Doxorubicin[J].Biomagnetism,2011(6):1030-1032.
Authors:YU Fang  CHEN Xie-qun  CHEN Juan-juan  HUANG Xiao-mei
Institution:(Department of Hematology,Xijing Hospital,Fourth Military Medical University,Xi'an 710032,China)
Abstract:Objective:As a major intracellular degradation system that is found ubiquitously in eukaryotes,autophagy plays a key role in maintaining protein metabolic equilibrium,cell homeostasis,regulating cellular constituent recycling,cell development and differ-entiation.In different cell types or different stress modes,the role or function of autophagy changes.What's the function of autophagy in myeloma cells? We don't have experience at present.Based on the background above,in this study,by means of the model of myeloma cells(H-929 cells),we try to explore the effects of autophagy on cell death induced by DOXO and the correlating mechanism.Methods:After treated with DOXO(2umol/l for 24 h) with or without 3MA(10mmol/l),cells were collected and subjected to MTT assay,cellular ATP measurement and western blot for analysis.The ATP level was presented as percentage to the untreated control group.Results:The survival ratio was significantly higher in the DOXO group(54%) than that in the DOXO+3-MA group(35%);The ATP level changed(DOXO group 400%,DOXO+3-MA group 150%);Western blot showed that there was a high level of LC3II in DOXO singly treating cells and a low level in DOXO+3-MA group.Conclusions:1.Autophagy as protective mechanism responses to the death induced by DOXO;2.Autophagy inhibition by chemical inhibitor enhances the death induced by DOXO in myeloma cell lines;3.It has a relation with ATP.
Keywords:Doxorubicin  Multiple myeloma  ATP  Autophagy  NCI-H929 cell  LC3
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