Damage to mitochondrial respiration chain is related to phospholipase A2 activation caused by tumor necrosis factor.

M Higuchi, K Shirotani, N Higashi, S Toyoshima, T Osawa
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引用次数: 17

Abstract

Tumor necrosis factor (TNF) has been shown to be cytotoxic to tumor cell lines in vitro, but the mechanism by which TNF exerts its cell growth-regulatory effects is not known. In this report, we used various inhibitors to investigate the sequence of events that lead to cytotoxic effects of TNF on L.P3 cells, a highly sensitive, murine fibroblast cell line. Our results indicate that mitochondrial respiration chains are damaged by a hydroxyl radical at an early stage of the cell lysis after TNF treatment. This event is followed by the activation of phospholipase A2, and finally leads to cell lysis.

线粒体呼吸链损伤与肿瘤坏死因子引起的磷脂酶A2活化有关。
肿瘤坏死因子(Tumor necrosis factor, TNF)在体外已被证明对肿瘤细胞系具有细胞毒性,但TNF发挥其细胞生长调节作用的机制尚不清楚。在本报告中,我们使用各种抑制剂来研究导致TNF对L.P3细胞(一种高度敏感的小鼠成纤维细胞系)细胞毒性作用的事件序列。我们的研究结果表明,线粒体呼吸链在TNF治疗后细胞裂解的早期阶段被羟基自由基破坏。这一事件随后是磷脂酶A2的激活,并最终导致细胞裂解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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