期刊文献+

Flow Cytometric Evidence for Hydroxyl Radical-induced Apoptosis in Tobacco Protoplasts 被引量:4

羟自由基诱导的烟草原生质体的凋亡:流式细胞法的新证据(英文)
下载PDF
导出
摘要 Protoplasts prepared from tobacco (Nicotiana tabacum L., cultivar BY-2) suspension cells have similar morphological characteristics to those in animal cells. The hallmarks of apoptosis such as condensation and peripheral distribution of nuclei, TUNEL positive reaction, and DNA ladders were observed when tobacco protoplasts were treated with the hydroxyl radical generating system (1.0 mmol/L FeSO4/0.5 mmol/L H2O2). In animals, the loss of transmembrane potential (DeltaPsi(m)) and the exposure of phospholipid phosphatidylserine (PS) are believed to be the main apoptosis events. To test whether these significant processes take place in plants, flow cytometry was used to detect annexin V binding and changes in DeltaPsi(m). Results showed that the PS turned out from inner membrane and DeltaPsi(m) gradually decreased during the apoptosis. All these apoptotic characteristics proved that hydroxyl radicals can cause typical programmed cell death (PCD) in tobacco protoplasts and this design can be served as an effective experiment system to explore the mechanism of plant apoptosis. 用1.0mmol/L FeSO_4/0.5mmol/L H_2O_2处理烟草(Nicotiana tabacum L.,cultivar BY-2)原生质体,发现羟自由基能够诱导烟草原生质体的凋亡。具体表现为细胞核皱缩、DNA Ladder、TUNEL阳性反应等典型的凋亡特征。在动物细胞凋亡过程中,线粒体起着非常重要的作用,其中膜电位(ΔΨ_m)的变化以及由其引起的位于线粒体膜上的通透性孔(PTP)的开放与Cyt c的释放有关。另外,在动物凋亡细胞中,磷脂酰丝氨酸(phosphatidylserine,PS)会从细胞膜内侧向外翻转。为了判断植物细胞凋亡过程中膜电位的变化情况以及PS的外翻程度,我们采用了流式细胞法。结果表明,随着处理时间的延长,烟草原生质体线粒体的膜电位逐渐降低;膜内PS大量外翻。说明由羟自由基和烟草原生质体组成的凋亡体系是一种可靠的凋亡组合,可以用来对植物细胞凋亡机理做进一步研究。
出处 《Acta Botanica Sinica》 CSCD 2003年第8期944-948,共5页 Acta Botanica Sinica(植物学报:英文版)
关键词 tobacco protoplasts flow cytometry APOPTOSIS programmed cell death (PCD) hydroxyl radicals 羟自由基 烟草原生质体 流式细胞法 细胞调亡 程序性细胞死亡
  • 相关文献

参考文献18

  • 1[1]Bernardi P, Broekemeier K M, Pfeiffer D R. 1994. Recentprogress on regulation of the mitochondrial permeability tran sition pore: a cyclosporine-sensitive pore in the inner mitochondrial-membrane. Bioenerg Biomembe, 26:509-517.
  • 2[2]Bossy W E, Newmeyer D D, Green D R. 1998. Mitochondrial cytochrome c release in apoptosis occurs upstream of DEVDspecific caspase activation and independently ofmitochon drial transmembrane depolarization. EMBO J, 17:37-49.
  • 3[3]Fulda S, Scaffidi C, Susin S A, Krammer P H, Kroemer G, Peter M E, Debatin K M. 1998. Activation of mitochondria andrelease ofmitochondrial apoptogenic factors by betulinic acid.JBiol Chem, 273:33942-33948.
  • 4[4]Jones A M, Dangl J L. 1996. Logjam at the styx: programmed cell death in plants. Trends Plant Sci, 1:114-119.
  • 5[5]Kluck R M, Martin S J, Homan B M, Zhou J S, Green D R, Newmeyer D D. 1997. Cytochrome c activation of CPP32-like proteolysis plays a critical role in a Xenopus cell-freeapoptosis system. EMBO J, 16:4639-4649.
  • 6[6]Mittler R. 1998. Cell Death in Plants: a Comprehensive Evalu ation of Apoptosis and PCD. New York: Wiley-Liss. 147-174.
  • 7[7]O'Brien I E W, Reutelingsperger C P M, Holdaway K M. 1997.The use of annexin V and TUNEL to monitor the progression of apoptosis in plants. Cytometry, 29:28-33.
  • 8[8]Pennell R I, Lamb C. 1997. Programmed cell death in plants.Plant Cell, 9:1157-1168.
  • 9[9]Ren J G, Xia H L, Just T, Dai Y R. 2001. Hydroxyl radicalinduced apoptosis in human tumor cells is associated with telomere shortening but not telomerase inhibition and caspaseactivation. FEBS Lett, 488:123-132.
  • 10[10]Ryerson D E, Heath M C. 1996. Cleavage of nuclear DNA into oligonucleosomal fragments during cell death induced by fun gal infection or by abiotic treatments. Plant Cell, 8:393-402.

同被引文献64

引证文献4

二级引证文献19

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部