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肾上皮细胞系NBL-1中B0型氨基酸转运活性的调节及SAAT1杂交转录本的伴随变化。

Regulation of System B0 amino-acid-transport activity in the renal epithelial cell line NBL-1 and concomitant changes in SAAT1 hybridizing transcripts.

作者信息

Plakidou-Dymock S, Tanner M J, McGivan J D

机构信息

Department of Biochemistry, University of Bristol, School of Medical Sciences, U.K.

出版信息

Biochem J. 1994 Jul 15;301 ( Pt 2)(Pt 2):399-405. doi: 10.1042/bj3010399.

Abstract

alpha-(Methylamino)isobutyric acid (MeAIB) insensitive Na(+)-dependent alanine transport activity in the bovine kidney cell line NBL-1 was increased upon amino acid starvation (> or = 20% over control levels). When L-phenylalanine (3 mM) was included in the starvation medium the increase was further enhanced (> or = 85% over control levels). In cells grown in control medium the Vmax, for MeAIB-insensitive Na+/alanine co-transport was found to be 6.0 +/- 0.7 nmol/3 min per mg (Km 41 +/- 12 microM) and for L-phenylalanine-treated amino-acid-starved cells the Vmax. was 21 +/- 5 nmol/3 min per mg (Km 92 +/- 40 microM). The increase in Vmax. was prevented by cycloheximide. Substrate specificity analysis identified the L-phenylalanine-induced transport system as System B0. [35S]Methionine labelling of cells during the amino acid starvation/phenylalanine treatments resulted in the differential labelling of a protein of 78 kDa. Northern-blot analysis using a SAAT1-specific probe revealed the presence of a new transcript (3.2 kb) in RNA extracted from cells incubated in amino acid starvation medium with L-phenylalanine included. The present findings suggest a novel means of control for System B0 by the use of physiological stress. It is also proposed that SAAT1 and System-B0 transcripts have considerable sequence similarity.

摘要

在牛肾细胞系NBL-1中,α-(甲基氨基)异丁酸(MeAIB)不敏感的Na⁺依赖性丙氨酸转运活性在氨基酸饥饿时增加(比对照水平高≥20%)。当饥饿培养基中加入L-苯丙氨酸(3 mM)时,这种增加进一步增强(比对照水平高≥85%)。在对照培养基中生长的细胞中,发现MeAIB不敏感的Na⁺/丙氨酸共转运的Vmax为6.0±0.7 nmol/3 min per mg(Km为41±12 μM),而对于L-苯丙氨酸处理的氨基酸饥饿细胞,Vmax为21±5 nmol/3 min per mg(Km为92±40 μM)。Vmax的增加被环己酰亚胺阻止。底物特异性分析确定L-苯丙氨酸诱导的转运系统为系统B0。在氨基酸饥饿/苯丙氨酸处理期间用[³⁵S]甲硫氨酸标记细胞,导致对一种78 kDa蛋白质的差异标记。使用SAAT1特异性探针的Northern印迹分析显示,在用含L-苯丙氨酸的氨基酸饥饿培养基孵育的细胞提取的RNA中存在一种新的转录本(3.2 kb)。目前的研究结果表明,通过生理应激对系统B0进行控制的一种新方法。还提出SAAT1和系统B0转录本具有相当大的序列相似性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eaa/1137094/4cce676094ae/biochemj00083-0092-a.jpg

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