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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >The synthesis of SNAT2 transporters is required for the hypertonic stimulation of system A transport activity
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The synthesis of SNAT2 transporters is required for the hypertonic stimulation of system A transport activity

机译:高渗刺激系统A转运活性需要SNAT2转运蛋白的合成

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摘要

In cultured human fibroblasts incubated under hypertonic conditions, the stimulation of system A for neutral amino acid transport, associated to the increased expression of the mRNA for SNAT2 transporter, leads to an expanded intracellular amino acid pool and to the recovery of cell volume. A protein of nearly 60 kDa, recognized by an antiserum against SNAT2, is increased both in the pool of biotinylated membrane proteins and in the total cell lysate of hypertonically stressed cells. The increased level of SNAT2 transporters in hypertonically stressed cells is confirmed by immunocytochemistry. DRB, an inhibitor of transcription, substantially inhibits the increase of SNAT2 proteins on the plasma membrane, completely suppresses the stimulation of system A transport activity, and markedly delays the cell volume recovery observed during the hypertonic treatment. On the contrary, if the transport activity of system A is adaptively increased by amino acid starvation in the presence of DRB, the increase of SNAT2 transporters on the plasma membrane is still clearly detectable and the transport change only partially inhibited. It is concluded that the synthesis of new SNAT2 transporters is essential for the hypertonic stimulation of transport system A, but accounts only in part for the adaptive increase of the system. (C) 2004 Elsevier B.V. All rights reserved.
机译:在高渗条件下培养的培养的人类成纤维细胞中,刺激系统A进行中性氨基酸转运,与SNAT2转运蛋白的mRNA表达增加相关,导致细胞内氨基酸池扩大和细胞体积恢复。被SNAT2抗血清识别的近60 kDa的蛋白质在生物素化膜蛋白库和高渗应激细胞的总细胞裂解物中均增加。免疫细胞化学证实高渗应激细胞中SNAT2转运蛋白水平增加。 DRB是一种转录抑制剂,基本上抑制了质膜上SNAT2蛋白的增加,完全抑制了系统A转运活性的刺激,并显着延迟了高渗治疗期间观察到的细胞体积恢复。相反,如果在DRB存在下氨基酸饥饿使系统A的转运活性适应性地增加,则质膜上SNAT2转运蛋白的增加仍可清楚地检测到,而转运变化仅被部分抑制。结论是,新的SNAT2转运蛋白的合成对于转运系统A的高渗刺激是必不可少的,但仅部分解释了系统的适应性增加。 (C)2004 Elsevier B.V.保留所有权利。

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