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首页> 外文期刊>American Journal of Physiology >Effects of glutamine deprivation on protein synthesis in a model of human enterocytes in culture.
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Effects of glutamine deprivation on protein synthesis in a model of human enterocytes in culture.

机译:谷氨酰胺剥夺对培养的人类肠上皮细胞模型蛋白质合成的影响。

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To assess the effect of glutamine availability on rates of protein synthesis in human enterocytes, Caco-2 cells were grown until differentiation and then submitted to glutamine deprivation produced by exposure to glutamine-free medium or methionine sulfoximine [L-S-[3-amino-3-carboxypropyl]-S-methylsulfoximine (MSO)], a glutamine synthetase inhibitor. Cells were then incubated with (2)H(3)-labeled leucine with or without glutamine, and the fractional synthesis rate (FSR) of total cell protein was determined from (2)H(3)-labeled enrichments in protein-bound and intracellular free leucine measured by gas chromatography-mass spectrometry. Both protein FSR (28 +/- 1.5%/day) and intracellular glutamine concentration (6.1 +/- 0.6 micromol/g protein) remained unaltered when cells were grown in glutamine-free medium. In contrast, MSO treatment resulted in a dramatic reduction in protein synthesis (4.6 +/- 0.6 vs. 20.2 +/- 0.8%/day, P < 0.01). Supplementation with 0.5-2 mM glutamine for 4 h after MSO incubation, but not with glycine nor glutamate, restored protein FSR to control values (24 +/- 1%/day). These results demonstrate that in Caco-2 cells, 1) de novo glutamine synthesis is highly active, since it can maintain intracellular glutamine pool during glutamine deprivation, 2) inhibition of glutamine synthesis is associated with reduced protein synthesis, and 3) when glutamine synthesis is depressed, exogenous glutamine restores normal intestinal FSR. Due to the limitations intrinsic to the use of a cell line as an experimental model, the physiological relevance of these findings for the human intestine in vivo remains to be determined.
机译:为了评估谷氨酰胺可用性对人肠上皮细胞蛋白质合成速率的影响,使Caco-2细胞生长直至分化,然后通过暴露于无谷氨酰胺的培养基或蛋氨酸硫代亚胺[LS- [3-amino-3 -羧丙基] -S-甲基磺酰亚胺(MSO)],一种谷氨酰胺合成酶抑制剂。然后将细胞与(2)H(3)标记的有或没有谷氨酰胺的亮氨酸一起孵育,并根据(2)H(3)标记的蛋白质结合和蛋白质富集度确定总细胞蛋白的分数合成速率(FSR)。气相色谱-质谱法测定细胞内游离亮氨酸。当细胞在无谷氨酰胺的培养基中生长时,蛋白质FSR(28 +/- 1.5%/天)和细胞内谷氨酰胺浓度(6.1 +/- 0.6 micromol / g蛋白质)都保持不变。相反,MSO处理导致蛋白质合成显着降低(4.6 +/- 0.6对20.2 +/- 0.8%/天,P <0.01)。 MSO孵育后4小时补充0.5-2 mM谷氨酰胺,但不补充甘氨酸或谷氨酸,则将蛋白FSR恢复至对照值(24 +/- 1%/天)。这些结果表明,在Caco-2细胞中,1)从头谷氨酰胺合成非常活跃,因为它可以在谷氨酰胺剥夺期间维持细胞内谷氨酰胺库; 2)抑制谷氨酰胺合成与蛋白质合成减少有关;以及3)当谷氨酰胺合成时如果情绪低落,外源性谷氨酰胺可恢复正常的肠道FSR。由于使用细胞系作为实验模型所固有的局限性,这些发现与人体在体内的生理相关性仍有待确定。

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