Effects of hypoxia on the cytotoxicity mediated by tumor necrosis factor-alpha.

Lymphokine and cytokine research Pub Date : 1994-08-01
A Naldini, S Cesari, V Bocci
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引用次数: 0

Abstract

We investigated whether hypoxia (2% O2, approximately 14 mm Hg partial pressure) in comparison to O2 atmospheric pressure (20.9% O2, approximately 140 mm Hg) can affect the cytotoxic effects of tumor necrosis factor-alpha (TNF) on the murine cell line L929. Under hypoxic conditions, L929 cells were significantly less inhibited by TNF treatment, even in the presence of actinomycin D. Moreover, under hypoxic conditions, TNF cytotoxicity was significantly inhibited by glutathione, which has been shown to protect cells against oxidative damage induced by various agents. On the other hand, under aerobic conditions treatment with other antioxidant agents and active species oxygen scavengers, as superoxide dismutase and catalase, did not markedly affect the cytotoxicity of TNF. Since hypoxia occurs normally in most solid tumors, these results are interesting because they suggest a disadvantageous inhibition of the cytotoxic effects of TNF in vivo in hypoxic tissues and confirm that oxygen-dependent metabolic processes or free radicals are required to exert TNF-induced cytotoxicity.

缺氧对肿瘤坏死因子- α介导的细胞毒性的影响。
我们研究了缺氧(2% O2,约14毫米汞柱分压)与O2大气压(20.9% O2,约140毫米汞柱)是否会影响肿瘤坏死因子- α (TNF)对小鼠细胞系L929的细胞毒性作用。在缺氧条件下,即使放线菌素d存在,TNF处理对L929细胞的抑制作用也明显减弱。此外,在缺氧条件下,谷胱甘肽显著抑制TNF的细胞毒性,谷胱甘肽已被证明可以保护细胞免受各种药物诱导的氧化损伤。另一方面,在好氧条件下,使用其他抗氧化剂和活性氧清除剂,如超氧化物歧化酶和过氧化氢酶,对TNF的细胞毒性没有显著影响。由于缺氧通常发生在大多数实体肿瘤中,这些结果很有趣,因为它们表明在体内缺氧组织中对TNF的细胞毒性作用有不利的抑制作用,并证实了依赖氧的代谢过程或自由基是发挥TNF诱导的细胞毒性所必需的。
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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