Suppr超能文献

细胞对铁缺乏诱导的细胞凋亡的敏感性可因铁的可利用性而发生可逆性改变。

Sensitivity of cells to apoptosis induced by iron deprivation can be reversibly changed by iron availability.

作者信息

Koc M, Nad'ová Z, Kovár J

机构信息

Department of Cell Signalling and Apoptosis, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Prague, Czech Republic.

出版信息

Cell Prolif. 2006 Dec;39(6):551-61. doi: 10.1111/j.1365-2184.2006.00411.x.

Abstract

We tested the effect of iron deprivation on cell death induction in human Raji cells pre-adapted to differing availability of extracellular iron. Iron deprivation was achieved by incubation in a defined iron-free medium. Original Raji cells have previously been adapted to long-term culture in a defined medium with 5 microg/ml of iron-saturated human transferrin as a source of iron. Raji/lowFe cells were derived from original Raji cells by subsequent adaptation to culture in the medium with 50 microm ferric citrate as a source of iron. Raji/lowFe-re cells were derived from Raji/lowFe cells by re-adaptation to the transferrin-containing (5 microg/ml) medium. Iron deprivation induced cell death in both Raji cells and Raji/lowFe-re cells; that is, cells pre-adapted to a near optimum source of extracellular iron (5 microg/ml of transferrin). However, Raji/lowFe cells preadapted to a limited source of extracellular iron (50 microm ferric citrate) became resistant to the induction of cell death by iron deprivation. We demonstrated that cell death induction by iron deprivation in Raji cells correlates with the activation of executioner caspase-3 and the cleavage of caspase-3 substrate, poly-ADP ribose polymerase. Two other executioner caspases, caspase-7 and caspase-6, were not activated. Taken together, we suggest that in human Raji cells, iron deprivation induces apoptotic cell death related to caspase-3 activation. However, the sensitivity of the cells to death induction by iron deprivation can be reversibly changed by extracellular iron availability. The cells pre-adapted to a limited source of extracellular iron became resistant.

摘要

我们测试了铁剥夺对预先适应不同细胞外铁可用性的人Raji细胞中细胞死亡诱导的影响。通过在特定的无铁培养基中孵育来实现铁剥夺。原始的Raji细胞先前已适应在含有5微克/毫升铁饱和人转铁蛋白作为铁源的特定培养基中进行长期培养。Raji/lowFe细胞是通过随后适应在含有50微摩尔柠檬酸铁作为铁源的培养基中培养而从原始Raji细胞衍生而来。Raji/lowFe-re细胞是通过重新适应含转铁蛋白(5微克/毫升)的培养基从Raji/lowFe细胞衍生而来。铁剥夺在Raji细胞和Raji/lowFe-re细胞中均诱导细胞死亡;也就是说,这些细胞预先适应了接近最佳的细胞外铁源(5微克/毫升转铁蛋白)。然而,预先适应有限细胞外铁源(50微摩尔柠檬酸铁)的Raji/lowFe细胞对铁剥夺诱导的细胞死亡产生了抗性。我们证明,Raji细胞中铁剥夺诱导的细胞死亡与执行蛋白酶caspase-3的激活以及caspase-3底物聚ADP核糖聚合酶的裂解相关。另外两种执行蛋白酶caspase-7和caspase-6未被激活。综上所述,我们认为在人Raji细胞中,铁剥夺诱导与caspase-3激活相关的凋亡性细胞死亡。然而,细胞对铁剥夺诱导死亡的敏感性可因细胞外铁的可用性而可逆地改变。预先适应有限细胞外铁源的细胞变得具有抗性。

相似文献

1
Sensitivity of cells to apoptosis induced by iron deprivation can be reversibly changed by iron availability.
Cell Prolif. 2006 Dec;39(6):551-61. doi: 10.1111/j.1365-2184.2006.00411.x.
2
Differing sensitivity of tumor cells to apoptosis induced by iron deprivation in vitro.
In Vitro Cell Dev Biol Anim. 2001 Jul-Aug;37(7):450-8. doi: 10.1290/1071-2690(2001)037<0450:DSOTCT>2.0.CO;2.
4
Iron deprivation induces apoptosis via mitochondrial changes related to Bax translocation.
Apoptosis. 2005 Mar;10(2):381-93. doi: 10.1007/s10495-005-0812-8.
10
Iron deprivation induces apoptosis independently of p53 in human and murine tumour cells.
Cell Prolif. 2003 Aug;36(4):199-213. doi: 10.1046/j.1365-2184.2003.00280.x.

本文引用的文献

2
Targeting apoptosis pathways in cancer therapy.
CA Cancer J Clin. 2005 May-Jun;55(3):178-94. doi: 10.3322/canjclin.55.3.178.
3
Iron deprivation induces apoptosis via mitochondrial changes related to Bax translocation.
Apoptosis. 2005 Mar;10(2):381-93. doi: 10.1007/s10495-005-0812-8.
4
Apoptosis, pyroptosis, and necrosis: mechanistic description of dead and dying eukaryotic cells.
Infect Immun. 2005 Apr;73(4):1907-16. doi: 10.1128/IAI.73.4.1907-1916.2005.
5
Recent advances in understanding the cell death pathways activated by anticancer therapy.
Cancer. 2005 Apr 15;103(8):1551-60. doi: 10.1002/cncr.20947.
7
Iron deprivation induces apoptosis independently of p53 in human and murine tumour cells.
Cell Prolif. 2003 Aug;36(4):199-213. doi: 10.1046/j.1365-2184.2003.00280.x.
8
Caspase-independent cell death in T lymphocytes.
Nat Immunol. 2003 May;4(5):416-23. doi: 10.1038/ni0503-416.
9
The role of iron in cell cycle progression and the proliferation of neoplastic cells.
Biochim Biophys Acta. 2002 Oct 2;1603(1):31-46. doi: 10.1016/s0304-419x(02)00068-9.
10
Antiproliferative and apoptotic effects of iron chelators on human cervical carcinoma cells.
Gynecol Oncol. 2002 Apr;85(1):95-102. doi: 10.1006/gyno.2001.6570.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验