中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
ER stress-mediated apoptosis induced by celastrol in cancer cells and important role of glycogen synthase kinase-3 beta in the signal network

文献类型:期刊论文

作者Feng, L.2; Zhang, D.2; Fan, C.2; Ma, C.3; Yang, W.1; Meng, Y.2; Wu, W.2; Guan, S.2; Jiang, B.2; Yang, M.2
刊名CELL DEATH & DISEASE
出版日期2013-07
卷号4
关键词celastrol apoptosis endothelium reticulum proteomics bioinformatics
ISSN号2041-4889
DOI10.1038/cddis.2013.222
文献子类Article
英文摘要HeLa cells treated with celastrol, a natural compound with inhibitive effect on proteasome, exhibited increase in apoptotic rate and characteristics of apoptosis. To clarify the signal network activated by celastrol to induce apoptosis, both the direct target proteins and undirect target proteins of celastrol were searched in the present study. Proteasome catalytic subunit beta 1 was predicted by computational analysis to be a possible direct target of celastrol and confirmed by checking direct effect of celastrol on the activity of recombinant human proteasome subunit beta 1 in vitro. Undirect target-related proteins of celastrol were searched using proteomic studies including two-dimensional electrophoresis (2-DE) analysis and iTRAQ-based LC-MS analysis. Possible target-related proteins of celastrol such as endoplasmic reticulum protein 29 (ERP29) and mitochondrial import receptor Tom22 (TOM22) were found by 2-DE analysis of total cellular protein expression profiles. Further study showed that celastrol induced ER stress and ER stress inhibitor could ameliorate cell death induced by celastrol. Celastrol induced translocation of Bax into the mitochondria, which might be related to the upregulation of BH-3-only proteins such as BIM and the increase in the expression level of TOM22. To further search possible target-related proteins of celastrol in ER and ER-related fractions, iTRAQ-based LC-MS method was use to analyze protein expression profiles of ER/microsomal vesicles-riched fraction of cells with or without celastrol treatment. Based on possible target-related proteins found in both 2-DE analysis and iTRAQ-based LC-MS analysis, protein-protein interaction (PPI) network was established using bioinformatic analysis. The important role of glycogen synthase kinase-3 beta (GSK3 beta) in the signal cascades of celastrol was suggested. Pretreatment of LiCL, an inhibitor of GSK3 beta, could significantly ameliorate apoptosis induced by celastrol. On the basis of the results of the present study, possible signal network of celastrol activated by celastrol leading to apoptosis was predicted.
WOS关键词INDUCED CASPASE-3 ACTIVATION ; THUNDER GOD VINE ; KINASE 3-BETA ; TOM COMPLEX ; MOLECULAR TARGETS ; HSP90 INHIBITOR ; OUTER-MEMBRANE ; IN-VIVO ; MITOCHONDRIA ; BAX
资助项目Chinese Academy of Sciences[KSCX2-YW-R-166] ; Twelfth Five-Year National Science and Technology Support Program[2012BAI29B06] ; National Natural Science Foundation of China[30960450] ; Yunnan Provincial Science and Technology Department[2011FA022]
WOS研究方向Cell Biology
语种英语
WOS记录号WOS:000322512100016
出版者NATURE PUBLISHING GROUP
源URL[http://119.78.100.183/handle/2S10ELR8/277552]  
专题上海中药现代化研究中心
天然药物化学研究室
分析化学研究室
药物安全性评价中心
通讯作者Liu, X.
作者单位1.Kunming Med Coll, Yunnan Pharmacol Labs Nat Prod, Kunming 650031, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China;
3.Tongji Univ, Sch Life Sci & Technol, Shanghai 200092, Peoples R China;
推荐引用方式
GB/T 7714
Feng, L.,Zhang, D.,Fan, C.,et al. ER stress-mediated apoptosis induced by celastrol in cancer cells and important role of glycogen synthase kinase-3 beta in the signal network[J]. CELL DEATH & DISEASE,2013,4.
APA Feng, L..,Zhang, D..,Fan, C..,Ma, C..,Yang, W..,...&Guo, D..(2013).ER stress-mediated apoptosis induced by celastrol in cancer cells and important role of glycogen synthase kinase-3 beta in the signal network.CELL DEATH & DISEASE,4.
MLA Feng, L.,et al."ER stress-mediated apoptosis induced by celastrol in cancer cells and important role of glycogen synthase kinase-3 beta in the signal network".CELL DEATH & DISEASE 4(2013).

入库方式: OAI收割

来源:上海药物研究所

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