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肿瘤坏死因子-α在肿瘤相关氧分压下对肉瘤F细胞的细胞毒性作用。

Cytotoxic effect of tumour necrosis factor -alpha on sarcoma F cells at tumour relevant oxygen tensions.

作者信息

Lynch E M, Sampson L E, Khalil A A, Horsman M R, Chaplin D J

机构信息

CRC Gray Laboratory, Mount Venon Hospital, Northwood, England.

出版信息

Acta Oncol. 1995;34(3):423-7. doi: 10.3109/02841869509094002.

Abstract

We have investigated the response of a murine tumour cell line, the sarcoma F (SaF), to tumour necrosis factor-alpha (TNF) at oxygen tensions known to occur in vivo. Using the Eppendorf pO2 histograph, the oxygen status of SaF tumours grown in situ was assessed. The median pO2 of the SaF is less than 1% oxygen with over 90% of values at or below 15 mmHg (< 2% O2). SaF cells primed in vitro for 24 h at tumour relevant oxygen tensions required at least four times more TNF to reduce cell number to 50% of controls following a 24 h incubation period in 21% oxygen. Chronic exposure of SaF cells to hypoxia during several passages increased resistance to TNF more than 60-fold. The oxygen sensitizing effect is transient as the resistance of hypoxic cells to TNF was reversed after 24 h incubation in air. These data clearly show that oxygen tension is a key modulator of the cytotoxic action of this important cytokine.

摘要

我们研究了一种小鼠肿瘤细胞系——肉瘤F(SaF),在已知的体内发生的氧张力条件下对肿瘤坏死因子-α(TNF)的反应。使用Eppendorf pO2组织氧图谱仪,评估原位生长的SaF肿瘤的氧状态。SaF的中位pO2低于1%氧,超过90%的值处于或低于15 mmHg(<2% O2)。在肿瘤相关氧张力下体外预培养24小时的SaF细胞,在21%氧中孵育24小时后,要将细胞数量减少至对照的50%,所需的TNF至少是对照的四倍。在多次传代过程中,将SaF细胞长期暴露于低氧环境下,其对TNF的抗性增加了60多倍。氧敏化作用是短暂的,因为低氧细胞在空气中孵育24小时后,对TNF的抗性会逆转。这些数据清楚地表明,氧张力是这种重要细胞因子细胞毒性作用的关键调节因子。

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