Astrocyte glutamine synthetase: pivotal in health and disease

被引:168
作者
Rose, Christopher F. [1 ]
Verkhratsky, Alexei [2 ]
Parpura, Vladimir [3 ,4 ]
机构
[1] Ctr Hosp Univ Montreal CRCHUM, Hepato Neuro Lab, Hop St Luc, Montreal, PQ H2X 1P1, Canada
[2] Univ Manchester, Fac Life Sci, Manchester M13 9PL, Lancs, England
[3] Univ Alabama Birmingham, Dept Neurobiol, Atom Force Microscopy & Nanotechnol Labs, Ctr Glial Biol Med,Civitan Int Res Ctr,Evelyn McK, Birmingham, AL 35294 USA
[4] Univ Rijeka, Dept Biotechnol, Rijeka 51000, Croatia
基金
美国国家科学基金会; 加拿大健康研究院;
关键词
gamma-aminobutyric acid (GABA); ammonia; astrocyte; glutamate; glutamine; glutamine synthetase; TEMPORAL-LOBE EPILEPSY; BERGMANN GLIAL-CELLS; EXTRACELLULAR GLUTAMATE; NONVESICULAR RELEASE; CULTURED ASTROCYTES; PROTEIN OXIDATION; MAJOR DEPRESSION; MOUSE MODEL; BRAIN; TRANSPORTER;
D O I
10.1042/BST20130237
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
The multifunctional properties of astrocytes signify their importance in brain physiology and neurological function. In addition to defining the brain architecture, astrocytes are primary elements of brain ion, pH and neurotransmitter homoeostasis. GS (glutamine synthetase), which catalyses the ATP-dependent condensation of ammonia and glutamate to form glutamine, is an enzyme particularly found in astrocytes. GS plays a pivotal role in glutamate and glutamine homoeostasis, orchestrating astrocyte glutamate uptake/release and the glutamate-glutamine cycle. Furthermore, astrocytes bear the brunt of clearing ammonia in the brain, preventing neurotoxicity. The present review depicts the central function of astrocytes, concentrating on the importance of GS in glutamate/glutamine metabolism and ammonia detoxification in health and disease.
引用
收藏
页码:1518 / 1524
页数:7
相关论文
共 89 条
[1]   NONVESICULAR RELEASE OF NEUROTRANSMITTER [J].
ATTWELL, D ;
BARBOUR, B ;
SZATKOWSKI, M .
NEURON, 1993, 11 (03) :401-407
[2]   The Importance of astrocyte-derived purines in the modulation of sleep [J].
Blutstein, Tamara ;
Haydon, Philip G. .
GLIA, 2013, 61 (02) :129-139
[3]   Adenosine signaling and function in glial cells [J].
Boison, D. ;
Chen, J-F ;
Fredholm, B. B. .
CELL DEATH AND DIFFERENTIATION, 2010, 17 (07) :1071-1082
[4]   Identifying the direct effects of ammonia on the brain [J].
Bosoi, Cristina R. ;
Rose, Christopher F. .
METABOLIC BRAIN DISEASE, 2009, 24 (01) :95-102
[5]   THE GLIAL-CELL GLUTAMATE UPTAKE CARRIER COUNTERTRANSPORTS PH-CHANGING ANIONS [J].
BOUVIER, M ;
SZATKOWSKI, M ;
AMATO, A ;
ATTWELL, D .
NATURE, 1992, 360 (6403) :471-474
[6]   SYNAPTIC VESICLES IMMUNOISOLATED FROM RAT CEREBRAL-CORTEX CONTAIN HIGH-LEVELS OF GLUTAMATE [J].
BURGER, PM ;
MEHL, E ;
CAMERON, PL ;
MAYCOX, PR ;
BAUMERT, M ;
LOTTSPEICH, F ;
DECAMILLI, P ;
JAHN, R .
NEURON, 1989, 3 (06) :715-720
[7]   The glutamine commute: take the N line and transfer to the A [J].
Chaudhry, FA ;
Reimer, RJ ;
Edwards, RH .
JOURNAL OF CELL BIOLOGY, 2002, 157 (03) :349-355
[8]   Glutamine uptake by neurons: Interaction of protons with system a transporters [J].
Chaudhry, FA ;
Schmitz, D ;
Reimer, RJ ;
Larsson, P ;
Gray, AT ;
Nicoll, R ;
Kavanaugh, M ;
Edwards, RH .
JOURNAL OF NEUROSCIENCE, 2002, 22 (01) :62-72
[9]  
Chen Y, 1999, J NEUROSCI RES, V58, P599, DOI 10.1002/(SICI)1097-4547(19991115)58:4<599::AID-JNR13>3.0.CO
[10]  
2-W