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培养细胞中甘氨酸摄取受生长培养基氨基酸浓度调控的遗传控制证据。

Evidence for genetic control of glycine uptake in cultured cells, regulated by the amino acid concentration of the growth medium.

作者信息

Hume S P, Lamb J F

出版信息

J Physiol. 1976 Jul;259(1):83-101. doi: 10.1113/jphysiol.1976.sp011456.

Abstract
  1. Cultured cells were grown in various concentrations of amino acids for periods up to 3 days and the characteristics of the glycine transport system measured under fixed experimental conditions. During this time, the effect of enucleation, using cytochalasin B, and the effects of protein synthesis inhibitors (cycloheximide and actinomycin D) were investigated. 2. Glycine influx is regulated by the prior growth concentration of similarly transported amino acids. 3. The modification in transport involves primarily a change in Vmax (but also a change in Km in HeLa cells) and is effected within 2-10 hr after media change. Increased transport activity is calculated to be sufficient to compensate for the reduction in extracellular amino acid concentration, so that nearly normal influx values from media are maintained. Regulation over the range of concentrations studied is shown to be very accurate. 4. The nucleus is essential for the regulatory mechanism to function. It seems probable that mRNA synthesis is required for acquisition of increased transport activity and mRNA translation required for maintenance of normal activity. 5. The controlling factor in the regulatory mechanism appears unlikely to be intracellular pool size. Other possible signals are discussed.
摘要
  1. 将培养的细胞在不同浓度的氨基酸中培养长达3天,并在固定的实验条件下测量甘氨酸转运系统的特性。在此期间,研究了使用细胞松弛素B去核的效果以及蛋白质合成抑制剂(环己酰亚胺和放线菌素D)的作用。2. 甘氨酸流入受相似转运氨基酸的先前生长浓度调节。3. 转运的改变主要涉及Vmax的变化(在HeLa细胞中Km也有变化),并且在培养基更换后2 - 10小时内发生。计算得出增加的转运活性足以补偿细胞外氨基酸浓度的降低,从而使来自培养基的流入值维持在接近正常水平。在所研究的浓度范围内的调节显示非常精确。4. 细胞核对于调节机制发挥功能至关重要。似乎增加转运活性的获得可能需要mRNA合成,而维持正常活性可能需要mRNA翻译。5. 调节机制中的控制因素似乎不太可能是细胞内池大小。还讨论了其他可能的信号。

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