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缺氧对肿瘤坏死因子-α介导的细胞毒性的影响。

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

作者信息

Naldini A, Cesari S, Bocci V

机构信息

Institute of General Physiology, University of Siena, Italy.

出版信息

Lymphokine Cytokine Res. 1994 Aug;13(4):233-7.

PMID:7999923
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.

摘要

我们研究了与常压氧气(20.9% O₂,约140 mmHg)相比,低氧环境(2% O₂,约14 mmHg分压)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。在低氧条件下,即使存在放线菌素D,L929细胞受TNF处理的抑制作用也显著降低。此外,在低氧条件下,谷胱甘肽可显著抑制TNF的细胞毒性,谷胱甘肽已被证明可保护细胞免受多种试剂诱导的氧化损伤。另一方面,在有氧条件下,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)处理,并未显著影响TNF的细胞毒性。由于大多数实体瘤中通常会出现低氧情况,这些结果很有意思,因为它们表明在体内低氧组织中TNF的细胞毒性作用受到不利抑制,并证实了发挥TNF诱导的细胞毒性需要氧依赖的代谢过程或自由基。

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