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膜脂质组成和普鲁卡因对细胞热致死的影响。

The influence of membrane lipid composition and procaine on hyperthermic death of cells.

作者信息

Yatvin M B

出版信息

Int J Radiat Biol Relat Stud Phys Chem Med. 1977 Dec;32(6):513-21. doi: 10.1080/09553007714551301.

Abstract

The mechanism of hyperthermic killing, a component of some cancer therapy, is not known. Cell-survival curves during hyperthermic exposure can be used to elucidate the effects of membrane modifying procedures on cell death. Experiments were designed to test whether procedures that were reported to increase membrane fluidity also resulted in increased killing on hyperthermic exposure. An E. coli K12 mutant, K1060, is used to predictably alter the degree and amount of unsaturated fatty acids incorporated into membranes. Changing from an 18:1 to an 18:3 unsaturated fatty acid increases killing. Decreasing the amount of unsaturated fatty acid cells incorporated by increasing growth temperature decreases killing. Procaine, a drug known to decrease membrane viscosity, increases heat killing. These data are most simply explained by the hypothesis that membrane disorganization occurs as a result of temperature increasing to a point where a lipid transition causes a membrane structural change, which results in cell-death.

摘要

热疗杀伤作为某些癌症治疗的一个组成部分,其机制尚不清楚。热暴露期间的细胞存活曲线可用于阐明膜修饰程序对细胞死亡的影响。设计实验以测试据报道可增加膜流动性的程序是否也会导致热暴露时杀伤作用增强。使用大肠杆菌K12突变体K1060可预测地改变掺入膜中的不饱和脂肪酸的程度和数量。从不饱和脂肪酸18:1转变为18:3会增加杀伤作用。通过提高生长温度来减少细胞掺入的不饱和脂肪酸量会降低杀伤作用。普鲁卡因是一种已知可降低膜粘度的药物,它会增加热杀伤作用。这些数据最简单的解释是基于这样的假设:由于温度升高到脂质转变导致膜结构变化的程度,从而发生膜紊乱,进而导致细胞死亡。

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