Glutamine transport in C6 glioma cells

被引:13
作者
Dolinska, M [1 ]
Dybel, A [1 ]
Albrecht, J [1 ]
机构
[1] Polish Acad Sci, Med Res Ctr, Dept Neurotoxicol, PL-02106 Warsaw, Poland
关键词
glutamine transport; C6; cells; system ASC; system N; system L;
D O I
10.1016/S0197-0186(00)00017-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glutamine transport across the cell membranes of a variety of mammalian tissues is mediated by at least four transport systems: a sodium-independent system L, and sodium-dependent systems A, ASC and N, the latter occurring in different tissue-specific variants. In this study we assessed the contribution of these systems to the uptake of [H-3]glutamine in C6 rat glioma cells. The sodium-dependent uptake, which accounted for more than 80% of the total uptake, was not inhibited by 2-methylaminoisobutyric acid (MeAIB), indicating that system A was inactive, possibly being depressed by glutamine present in the culture medium. About 80% of the sodium-dependent uptake was mediated by system ASC, which differed from system ASC common to other CNS- and non-CNS tissues by its pH-dependence and partial lithium tolerance. The residual 20% of sodium-dependent uptake appeared to be mediated by system N, which was identified as a component resistant to inhibition by MeAIB + threonine. The system N in CS cells appeared to be neither fully compatible with the neuronal system Nb, nor with the N system described in astrocytes: it differed from the former in being strongly inhibited by histidine and showing fair tolerance for lithium, and from the latter in its pH-insensitivity and strong inhibition by glutamate. The sodium-independent glutamine uptake differed from the astrocytic or neuronal uptake in its relatively weak inhibition by system L substrates and a strong inhibition by system ASC substrates, indicating a possible contribution of a variant of the ASC system. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:139 / 146
页数:8
相关论文
共 36 条
[1]   GLUTAMINE TRANSPORT IN HUMAN SKELETAL-MUSCLE [J].
AHMED, A ;
MAXWELL, DL ;
TAYLOR, PM ;
RENNIE, MJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (06) :E993-E1000
[3]  
ARENANDER AT, 1980, BRAIN RES, V3, P401
[4]   GLUCOCORTICOID HORMONE MODULATION OF BOTH CELL-SURFACE AND CYTOSKELETON RELATED TO GROWTH-CONTROL OF RAT GLIOMA-CELLS [J].
ARMELIN, MCS ;
ARMELIN, HA .
JOURNAL OF CELL BIOLOGY, 1983, 97 (02) :459-465
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   ROLE OF AMINO-ACID-TRANSPORT AND COUNTERTRANSPORT IN NUTRITION AND METABOLISM [J].
CHRISTENSEN, HN .
PHYSIOLOGICAL REVIEWS, 1990, 70 (01) :43-77
[7]  
Collins CL, 1998, J CELL PHYSIOL, V176, P166, DOI 10.1002/(SICI)1097-4652(199807)176:1<166::AID-JCP18>3.0.CO
[8]  
2-5
[9]   ADAPTATION OF C6 GLIOMA-CELLS TO SERUM-FREE CONDITIONS LEADS TO THE EXPRESSION OF A MIXED ASTROCYTE-OLIGODENDROCYTE PHENOTYPE AND INCREASED PRODUCTION OF NEURITE-PROMOTING ACTIVITY [J].
COYLE, DE .
JOURNAL OF NEUROSCIENCE RESEARCH, 1995, 41 (03) :374-385
[10]   RESPONSES IN ASTROCYTIC C6 GLIOMA-CELLS TO ETHANOL AND DIBUTYRYL-CYCLIC-AMP [J].
DAVIES, DL ;
VERNADAKIS, A .
DEVELOPMENTAL BRAIN RESEARCH, 1986, 24 (1-2) :253-260