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L929细胞条件培养基通过诱导抗氧化酶保护RAW264.7细胞免受氧化损伤。

L929 cell conditioned medium protects RAW264.7 cells from oxidative injury through inducing antioxidant enzymes.

作者信息

Pang Z J, Chen Y, Zhou M

机构信息

Research Laboratory of Free Radical Medicine, The First Military Medical University, Guangzhou, People's Republic of China.

出版信息

Cytokine. 2000 Jul;12(7):944-50. doi: 10.1006/cyto.2000.0683.

Abstract

We have previously found that L929 cell conditioned medium (L929-CM) could protect mouse peritoneal macrophages from oxidative injury. To uncover the mechanism further, we investigated the effect of L929-CM on the oxidative injury caused by tbOOH to RAW264.7 cell lines. The results showed that L929-CM could protect RAW264.7 cells from oxidative injury (presented by cell morphology and cell survival rate), and L929-CM could also improve total superoxide dismutase (SOD), selenium-dependent and non-selenium-dependent glutathione peroxidase (SeGPx and non-SeGPx) activities in RAW264.7 cells. RT-PCR analysis showed that, L929-CM could induce plasma glutathione peroxidase (PLGPx) mRNA expression, while there was no inducing effect of L929-CM on phospholipid hydroperoxide glutathione peroxidase (PHGPx) mRNA expression in RAW264.7 cells. 5 microg/ml actinomycin D, 30 microg/ml cycloheximide (de novo protein synthesis inhibitor) and 50 microg/ml acetovanilone (intracellular superoxide anion production inhibitor) had no effects in attenuating the induction of PLGPx expression by L929-CM.

摘要

我们之前发现,L929细胞条件培养基(L929-CM)可以保护小鼠腹腔巨噬细胞免受氧化损伤。为了进一步揭示其机制,我们研究了L929-CM对叔丁基过氧化氢(tbOOH)所致RAW264.7细胞系氧化损伤的影响。结果显示,L929-CM可以保护RAW264.7细胞免受氧化损伤(通过细胞形态和细胞存活率体现),并且L929-CM还可以提高RAW264.7细胞中总超氧化物歧化酶(SOD)、硒依赖性和非硒依赖性谷胱甘肽过氧化物酶(SeGPx和非SeGPx)的活性。逆转录聚合酶链反应(RT-PCR)分析表明,L929-CM可以诱导血浆谷胱甘肽过氧化物酶(PLGPx)mRNA表达,而L929-CM对RAW264.7细胞中磷脂氢过氧化物谷胱甘肽过氧化物酶(PHGPx)mRNA表达没有诱导作用。5微克/毫升放线菌素D、30微克/毫升环己酰亚胺(从头合成蛋白抑制剂)和50微克/毫升乙酰香草酮(细胞内超氧阴离子产生抑制剂)对减弱L929-CM诱导的PLGPx表达均无作用。

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