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2'-脱氧腺苷诱导大鼠嗜铬细胞凋亡。

2'-deoxyadenosine induces apoptosis in rat chromaffin cells.

作者信息

Wakade A R, Guo X, Palmer K C, Kulkarni J S, Przywara D A, Wakade T D

机构信息

Department of Pharmacology, School of Medicine, Wayne State University, Detroit, Michigan 48201, USA.

出版信息

J Neurochem. 1996 Dec;67(6):2273-81. doi: 10.1046/j.1471-4159.1996.67062273.x.

DOI:10.1046/j.1471-4159.1996.67062273.x
PMID:8931458
Abstract

We show here that 2'-deoxyadenosine (2'-dAdo) but not adenosine was toxic to chromaffin cells of 3-4-week-old rat adrenal glands. More than 75% of the cells plated in culture gradually died over a 3-day period in the presence of 100 microM 2'-dAdo plus 3 microM deoxycoformycin (DCF). Morphological observations together with bisbenzimide staining and terminal deoxynucleotidyl transferase-mediated nick and labeling showed membrane blebbing, shrinkage of cell bodies, chromatin condensation, and DNA fragmentation, suggesting apoptosis-like cell death by 2'-dAdo. Lethal effects of 2'-dAdo were potentiated by DCF, a drug that inhibits adenosine deaminase. 2'-dAdo-prompted cell death was not prevented by inhibitors of nucleoside transporter (3 microM dilazep or 1 microM nitrobenzylthioinosine), precursors of pyrimidine nucleotide biosynthesis (300 microM uridine or 100 microM 2'-deoxycytidine), or 5 mM nicotinamide. Cells incubated with 2'-dAdo (100 and 300 microM) showed a three- and ninefold, respectively, increase in content of dATP, a product known to be an inhibitor of ribonucleotide reductase, an enzyme essential for DNA synthesis. Formation of dATP was completely prevented by iodotubercidin (ITu), a drug that inhibits phosphorylation of 2'-dAdo to dATP by nucleoside kinase. It is interesting that nanomolar concentrations of ITu also completely protected chromaffin cells from 2'-dAdo lethality. Our study demonstrates for the first time that mammalian adrenal chromaffin cells undergo apoptotic cell death by a natural nucleoside and suggests that this model could be used to study apoptosis and cell function.

摘要

我们在此表明,2'-脱氧腺苷(2'-dAdo)而非腺苷对3 - 4周龄大鼠肾上腺嗜铬细胞具有毒性。在含有100 microM 2'-dAdo加3 microM脱氧助间型霉素(DCF)的情况下,接种于培养物中的细胞超过75%在3天内逐渐死亡。形态学观察以及双苯甲酰亚胺染色和末端脱氧核苷酸转移酶介导的缺口平移和标记显示,细胞出现膜泡化、细胞体收缩、染色质凝聚和DNA片段化,提示2'-dAdo导致类似凋亡的细胞死亡。DCF是一种抑制腺苷脱氨酶的药物,它增强了2'-dAdo的致死作用。核苷转运体抑制剂(3 microM双嘧达莫或1 microM硝基苄基硫代肌苷)、嘧啶核苷酸生物合成前体(300 microM尿苷或100 microM 2'-脱氧胞苷)或5 mM烟酰胺均不能阻止2'-dAdo引发的细胞死亡。用2'-dAdo(100和300 microM)孵育的细胞,其dATP含量分别增加了三倍和九倍,dATP是一种已知的核糖核苷酸还原酶抑制剂,而核糖核苷酸还原酶是DNA合成所必需的一种酶。碘结核菌素(ITu)可完全阻止dATP的形成,ITu是一种抑制核苷激酶将2'-dAdo磷酸化为dATP的药物。有趣的是,纳摩尔浓度的ITu也能完全保护嗜铬细胞免受2'-dAdo的致死作用。我们的研究首次证明哺乳动物肾上腺嗜铬细胞可因一种天然核苷而发生凋亡性细胞死亡,并表明该模型可用于研究凋亡和细胞功能。

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2'-deoxyadenosine induces apoptosis in rat chromaffin cells.2'-脱氧腺苷诱导大鼠嗜铬细胞凋亡。
J Neurochem. 1996 Dec;67(6):2273-81. doi: 10.1046/j.1471-4159.1996.67062273.x.
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