•NO and oxyradical metabolism in new cell lines of rat brain capillary endothelial cells forming the blood-brain barrier

被引:41
作者
Blasig, IE
Giese, H
Schroeter, ML
Sporbert, A
Utepbergenov, DI
Buchwalow, IB
Neubert, K
Schönfelder, G
Freyer, D
Schimke, I
Siems, WE
Paul, M
Haseloff, RF
Blasig, R
机构
[1] Forschungsinst Mol Pharmakol, D-10315 Berlin, Germany
[2] Humboldt Univ, Berlin, Germany
[3] Max Delbruck Ctr Mol Med, Berlin, Germany
[4] Free Univ Berlin, Clin Clin Pharmacol & Toxicol, Berlin, Germany
关键词
nitric oxide; reactive oxygen species; immortalization; blood-brain barrier; brain capillary endothelial cells;
D O I
10.1006/mvre.2001.2318
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
To investigate the relevance of (NO)-N-circle and oxyradicals in the blood-brain barrier (BBB), differentiated and well-proliferating brain capillary endothelial cells (BCEC) are required. Therefore, rat BCEC (rBCEC) were transfected with immortalizing genes. The resulting lines exhibited endothelial characteristics (factor VIII, angiotensin-converting enzyme, high prostacyclin/thromboxane release rates) and BBB markers (,gamma -glutamyl transpeptidase, alkaline phosphatase). The control line rBCEC2 (mock transfected) revealed fibroblastoid morphology, less factor VIII, reduced gamma -glutamyl transpeptidase, weak radical defence, low prostanoid metabolism, and limited proliferation. Lines transfected with immortalizing genes (especially rBCEC4, polyoma virus large T antigen) conserved primary properties: epitheloid morphology, subcultivation with high proliferation rate under pure culture conditions, and powerful defence against reactive oxygen species (Mn-, Cu/Zn-superoxide dismutase, catalase, glutathione peroxidase, glutathione) effectively controlling radical metabolism. Only 100 muM H2O2 overcame this defence and stimulated the formation of eicosanoids similarly as in primary cells. Some BBB markers were expressed to a lower degree; however, cocultivation with astrocytes intensified these markers (e.g., alkaline phosphatase) and paraendothelial tightness, indicating induction of BBB properties. Inducible NO synthase was induced by a cytokine plus lipopolysaccharide mixture in all lines and primary cells, resulting in (NO)-N-circle release. Comparing the cell lines obtained, rBCEC4 are stable immortalized and reveal the best conservation of properties from primary cells, including enzymes producing or decomposing reactive species. These cells can be subcultivated in large amounts and, hence, they are suitable to study the role of radical metabolism in the BBB and in the cerebral microvasculature. (C) 2001 Academic Press.
引用
收藏
页码:114 / 127
页数:14
相关论文
共 37 条
[1]  
[Anonymous], 1996, Methods in nitric oxide research
[2]   ARTERIAL ENDOTHELIAL BARRIER DYSFUNCTION - ACTIONS OF HOMOCYSTEINE AND THE HYPOXANTHINE-XANTHINE OXIDASE FREE-RADICAL GENERATING-SYSTEM [J].
BERMAN, RS ;
MARTIN, W .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (04) :920-926
[3]  
Betz AL, 1996, ADV NEUROL, V71, P301
[4]   Uncoupling of mitochondrial oxidative phosphorylation alters lipid peroxidation-derived free radical production but not recovery of postischemic rat hearts and post-hypoxic endothelial cells [J].
Blasig, IE ;
Dickens, BF ;
Weglicki, WB ;
Kramer, JH .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1996, 161 :167-177
[5]  
BORGERDING RA, 1995, J NEUROCHEM, V65, P1342, DOI 10.1046/j.1471-4159.1995.65031342.x
[6]  
CHESNE C, 1993, ADV EXP MED BIOL, V331, P113
[7]   EFFECTS OF INHIBITION OF NITRIC-OXIDE SYNTHASE ON BLOOD-BRAIN-BARRIER TRANSPORT IN FOCAL CEREBRAL-ISCHEMIA [J].
CHI, OZ ;
WEI, HM ;
SINHA, AK ;
WEISS, HR .
PHARMACOLOGY, 1994, 48 (06) :367-373
[8]   Drug transport to the brain: Comparison between in vitro and in vivo models of the blood-brain barrier [J].
Dehouck, MP ;
Dehouck, B ;
Schluep, C ;
Lemaire, M ;
Cecchelli, R .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 3 (06) :357-365
[9]   EICOSANOID PRODUCTION BY RAT CEREBRAL ENDOTHELIAL-CELLS - STIMULATION BY LIPOPOLYSACCHARIDE, INTERLEUKIN-1 AND INTERLEUKIN-6 [J].
DEVRIES, HE ;
HOOGENDOORN, KH ;
VANDIJK, J ;
ZIJLSTRA, FJ ;
VANDAM, AM ;
BREIMER, DD ;
VANBERKEL, TJC ;
DEBOER, AG ;
KUIPER, J .
JOURNAL OF NEUROIMMUNOLOGY, 1995, 59 (1-2) :1-8
[10]  
DURIEUTRAUTMANN O, 1991, IN VITRO CELL DEV B, V27, P771