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过氧亚硝酸盐刺激U937细胞中胞质磷脂酶A2的活性:花生四烯酸的生成程度调节细胞存活或死亡之间的平衡。

Peroxynitrite stimulates the activity of cytosolic phospholipase A2 in U937 cells: the extent of arachidonic acid formation regulates the balance between cell survival or death.

作者信息

Tommasini I, Sestili P, Guidarelli A, Cantoni O

机构信息

Istituto di Farmacologia e Farmacognosia, Università degli Studi di Urbino, Via S Chiara, 27 - 61029 Urbino (PU), Italy.

出版信息

Cell Death Differ. 2002 Dec;9(12):1368-76. doi: 10.1038/sj.cdd.4401123.

Abstract

Peroxynitrite stimulates in U937 cells release of arachidonic acid (AA) sensitive to various phospholipase A(2) (PLA(2)) inhibitors, including arachidonyl trifluoromethyl ketone (AACOCF(3)), which specifically inhibits cytosolic PLA(2) (cPLA(2)). This response linearly increases using non toxic concentrations of the oxidant, and reaches a plateau at levels at which toxicity becomes apparent. Three separate lines of evidence are consistent with the notion that AA generated by cPLA(2) promotes survival in cells exposed to peroxynitrite. Firstly, toxicity was suppressed by nanomolar levels of exogenous AA, or by AA generated by the direct PLA(2) activator melittin. Secondly AACOCF(3), or other PLA(2) inhibitors, promoted cell death after exposure to otherwise non toxic concentrations of peroxynitrite; exogenous AA abolished the enhancing effects mediated by the PLA(2) inhibitors. Finally, U937 cells transfected with cPLA(2) antisense oligonucleotides were killed by concentrations of peroxynitrite that were non-toxic for cells transfected with nonsense oligonucleotides. This lethal response was insensitive to AACOCF(3) and prevented by exogenous AA.

摘要

过氧亚硝酸盐可刺激U937细胞释放花生四烯酸(AA),这种释放对包括花生四烯酰三氟甲基酮(AACOCF(3))在内的多种磷脂酶A(2)(PLA(2))抑制剂敏感,而花生四烯酰三氟甲基酮可特异性抑制胞质磷脂酶A(2)(cPLA(2))。使用无毒浓度的氧化剂时,这种反应呈线性增加,并在毒性明显的水平达到平台期。三条独立的证据支持以下观点:cPLA(2)产生的AA可促进暴露于过氧亚硝酸盐的细胞存活。首先,纳摩尔水平的外源性AA或直接PLA(2)激活剂蜂毒素产生的AA可抑制毒性。其次,AACOCF(3)或其他PLA(2)抑制剂在暴露于原本无毒浓度的过氧亚硝酸盐后会促进细胞死亡;外源性AA可消除PLA(2)抑制剂介导的增强作用。最后,用cPLA(2)反义寡核苷酸转染的U937细胞会被对用无义寡核苷酸转染的细胞无毒的过氧亚硝酸盐浓度杀死。这种致死反应对AACOCF(3)不敏感,外源性AA可预防。

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