中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Regulation of acetylcholinesterase expression by calcium signaling during calcium ionophore A23187-and thapsigargin-induced apoptosis

文献类型:期刊论文

作者Zhu, H; Gao, W; Jiang, H; Jin, QH; Shi, YF; Tsim, KWK; Zhang, XJ
刊名INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
出版日期2007
卷号39期号:1页码:93-108
关键词acetylcholinesterase apoptosis Ca2+ mRNA stability transcriptional activity
通讯作者Zhang, XJ (reprint author), Chinese Acad Sci, Grad Sch, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol,Lab Mol Cell Biol, 320 Yue Yang Rd, Shanghai 200031, Peoples R China.,xjzhang@sibs.ac.cn
英文摘要We have recently reported that acetylcholinesterase expression was induced during apoptosis in various cell types. In the current study we provide evidence to suggest that the induction of acetylcholinesterase expression during apoptosis is regulated by the mobilization of intracellular Ca2+. During apoptosis, treatment of HeLa and MDA-MB-435s cells with the calcium ionophore A23187 resulted in a significant increase in acetylcholinesterase mRNA and protein levels. Chelation of intracellular Ca2+ by BAPTA-AM (1,2-bis-(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid-acetoxymethyl ester), an intracellular Ca2+ chelator, inhibited acetyleholinesterase expression. A23187 also enhanced the stability of acetylcholinesterase mRNA and increased the activity of acetylcholinesterase promoter, effects that were blocked by BAPTA-AM. Perturbations of cellular Ca2+ homeostasis by thapsigargin resulted in the increase of acetylcholinesterase expression as well as acetylcholinesterase promoter activity during thapsigargin induced apoptosis in HeLa and MDA-MB-435s cells, effects that were also inhibited by BAPTA-AM. We further demonstrated that the transactivation of the human acetylcholinesterase promoter by A23187 and thapsigargin was partially mediated by a CCAAT motif within the -1270 to -1248 fragment of the human acetylcholinesterase promoter. This motif was able to bind to CCAAT binding factor (CBF/NF-Y). These results strongly suggest that cytosolic Ca2+ plays a key role in acetylcholinesterase regulation during apoptosis induced by A23187 and thapsigargin. (c) 2006 Elsevier Ltd. All rights reserved.
学科主题Biochemistry & Molecular Biology; Cell Biology
类目[WOS]Biochemistry & Molecular Biology ; Cell Biology
关键词[WOS]MESSENGER-RNA STABILITY ; AMYLOID-BETA-PEPTIDE ; INTRACELLULAR CALCIUM ; ENDOPLASMIC-RETICULUM ; TRANSCRIPTIONAL REGULATION ; MYOGENIC DIFFERENTIATION ; NEUROMUSCULAR-JUNCTIONS ; INHIBITOR THAPSIGARGIN ; NEUROBLASTOMA-CELLS ; HIPPOCAMPAL-NEURONS
收录类别SCI
语种英语
WOS记录号WOS:000241963000009
版本出版稿
源URL[http://202.127.25.143/handle/331003/1515]  
专题上海生化细胞研究所_上海生科院生化细胞研究所
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Zhu, H,Gao, W,Jiang, H,et al. Regulation of acetylcholinesterase expression by calcium signaling during calcium ionophore A23187-and thapsigargin-induced apoptosis[J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY,2007,39(1):93-108.
APA Zhu, H.,Gao, W.,Jiang, H.,Jin, QH.,Shi, YF.,...&Zhang, XJ.(2007).Regulation of acetylcholinesterase expression by calcium signaling during calcium ionophore A23187-and thapsigargin-induced apoptosis.INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY,39(1),93-108.
MLA Zhu, H,et al."Regulation of acetylcholinesterase expression by calcium signaling during calcium ionophore A23187-and thapsigargin-induced apoptosis".INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY 39.1(2007):93-108.

入库方式: OAI收割

来源:上海生物化学与细胞生物学研究所

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