1,25-dihydroxyvitamin D3 regulates the synthesis of γ-glutamyl transpeptidase and glutathione levels in rat primary astrocytes

被引:175
作者
Garcion, E [1 ]
Sindji, L [1 ]
Leblondel, G [1 ]
Brachet, P [1 ]
Darcy, F [1 ]
机构
[1] Ctr Hosp Univ, INSERM, U298, Angers, France
关键词
astrocytes; brain inflammation; nitric oxide; gamma-glutamyl transpeptidase; glutathione; vitamin D;
D O I
10.1046/j.1471-4159.1999.0730859.x
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
Astrocytes play a pivotal role in CNS detoxification pathways, where glutathione (GSH) is involved in the elimination of oxygen and nitrogen reactive species such as nitric oxide. We have previously demonstrated that the specific activity of gamma-glutamyl transpeptidase (gamma-GT), an enzyme of central significance in GSH metabolism, is regulated in vivo in astrocytes by 1,25-dihydroxyvitamin D-3 (1,25-D-3). The aim of the present work was to investigate, in primary cultures of newborn rat astrocytes, the effects of this hormone on gamma-GT synthesis and on GSH and nitrite levels after lipopolysaccharide (LPS) treatment. This study demonstrates that both gamma-GT gene expression and specific activity, induced by LPS, are potentiated by 1,25-D-3. In contrast, 1,25-D-3 does not regulate the expression of other enzymes involved in astrocyte detoxification processes, such as superoxide dismutase or GSH peroxidase. In parallel, 1,25-D, enhanced intracellular GSH pools and significantly reduced nitrite production induced by LPS. Taken together, these results suggest that gamma-GT, GSH, and 1,25-D-3 play a fundamental role in astrocyte detoxification pathways.
引用
收藏
页码:859 / 866
页数:8
相关论文
共 71 条
[1]   GAMMA-GLUTAMYL-TRANSFERASE TRANSPEPTIDASE (GAMMA-GT) AND MAINTENANCE OF THIOL POOLS IN TUMOR-CELLS RESISTANT TO ALKYLATING-AGENTS [J].
AHMAD, S ;
OKINE, L ;
WOOD, R ;
ALJIAN, J ;
VISTICA, DT .
JOURNAL OF CELLULAR PHYSIOLOGY, 1987, 131 (02) :240-246
[2]  
Alexianu ME, 1998, J NEUROSCI RES, V51, P58, DOI 10.1002/(SICI)1097-4547(19980101)51:1<58::AID-JNR6>3.0.CO
[3]  
2-K
[4]  
AUFFRAY C, 1980, EUR J BIOCHEM, V107, P303
[5]  
Back SA, 1998, J NEUROSCI, V18, P6241
[6]   Neurodegenerative disorders in humans: the role of glutathione in oxidative stress-mediated neuronal death [J].
Bains, JS ;
Shaw, CA .
BRAIN RESEARCH REVIEWS, 1997, 25 (03) :335-358
[7]  
BIDMON H-J, 1991, Molecular and Cellular Neuroscience, V2, P145, DOI 10.1016/1044-7431(91)90007-B
[8]   ENZYMATIC BARRIER PROTECTS BRAIN CAPILLARIES FROM LEUKOTRIENE C-4 [J].
BLACK, KL ;
BABA, T ;
PARDRIDGE, WM .
JOURNAL OF NEUROSURGERY, 1994, 81 (05) :745-751
[9]   Differential regulation of gamma-glutamylcysteine synthetase heavy and light subunit gene expression [J].
Cai, JX ;
Huang, ZZ ;
Lu, SC .
BIOCHEMICAL JOURNAL, 1997, 326 :167-172
[10]  
Cantorna MT, 1998, J IMMUNOL, V160, P5314