Activated astrocytes induce nitric oxide synthase-2 in cerebral endothelium via tumor necrosis factor alpha

被引:0
作者
Shafer, RA [1 ]
Murphy, S [1 ]
机构
[1] UNIV IOWA,DEPT PHARMACOL,COLL MED,IOWA CITY,IA 52242
关键词
nitric oxide; endothelial cell; cytokines; gene regulation; NF-kappa B; cell-cell interaction;
D O I
10.1002/(SICI)1098-1136(199712)21:4<370::AID-GLIA4>3.0.CO;2-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Astrocytes under pathological conditions become activated and produce a variety of cytokines and low molecular weight signal molecules, Previously we demonstrated that activated astrocytes release nitric oxide which can downregulate the expression of nitric oxide synthase (NOS)-2 in co-cultured cerebral endothelium, and also release a transcriptionally regulated factor that can induce NOS-2 expression in endothelium (Borgerding and Murphy: J Neurochem 65:1342, 1995). The activity of this NOS-2-inducing factor was impeded by inhibitors of tyrosine kinases and IUF-kappa B activation. Tumor necrosis factor (TNF alpha) alone, or in combination with IL-6, induced NOS-2 expression in endothelial cells. A neutralizing antibody against TNF alpha attenuated the NOS-2 expression in endothelial cells exposed, to activated astrocytes. These results imply that cytokine-activated astrocytes release TNF alpha which can induce NOS-2 expression in endothelium and suggest that activated astrocytes within the CNS may induce expression of NOS-2 in cells of the adjacent microvasculature. The ensuing alterations in blood-brain barrier properties may be either beneficial or detrimental. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:370 / 379
页数:10
相关论文
共 53 条
[1]   PATTERNS OF GLIOSIS IN ALZHEIMERS-DISEASE AND AGING CEREBRUM [J].
BEACH, TG ;
WALKER, R ;
MCGEER, EG .
GLIA, 1989, 2 (06) :420-436
[2]   TUMOR-NECROSIS-FACTOR AND INTERLEUKIN-1 LEAD TO PHOSPHORYLATION AND LOSS OF I-KAPPA-B-ALPHA - A MECHANISM FOR NF-KAPPA-B ACTIVATION [J].
BEG, AA ;
FINCO, TS ;
NANTERMET, PV ;
BALDWIN, AS .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (06) :3301-3310
[3]  
BORGERDING RA, 1995, J NEUROCHEM, V65, P1342, DOI 10.1046/j.1471-4159.1995.65031342.x
[4]   NITRIC-OXIDE - A PHYSIOLOGICAL MESSENGER MOLECULE [J].
BREDT, DS ;
SNYDER, SH .
ANNUAL REVIEW OF BIOCHEMISTRY, 1994, 63 :175-195
[5]   CLONED AND EXPRESSED NITRIC-OXIDE SYNTHASE STRUCTURALLY RESEMBLES CYTOCHROME-P-450 REDUCTASE [J].
BREDT, DS ;
HWANG, PM ;
GLATT, CE ;
LOWENSTEIN, C ;
REED, RR ;
SNYDER, SH .
NATURE, 1991, 351 (6329) :714-718
[6]  
CHUNG IY, 1990, J IMMUNOL, V144, P2999
[7]   Molecular mechanisms of TNF alpha cytotoxicity: Activation of NF-kappa B and nuclear translocation [J].
Claudio, E ;
Segade, F ;
Wrobel, K ;
Ramos, S ;
Bravo, R ;
Lazo, PS .
EXPERIMENTAL CELL RESEARCH, 1996, 224 (01) :63-71
[8]   EXPRESSION OF INDUCIBLE NITRIC-OXIDE SYNTHASE IN CYTOMEGALOVIRUS-INFECTED GLIAL-CELLS OF RETINAS FROM AIDS PATIENTS [J].
DIGHIERO, P ;
REUX, I ;
HAUW, JJ ;
FILLET, AM ;
COURTOIS, Y ;
GOUREAU, O .
NEUROSCIENCE LETTERS, 1994, 166 (01) :31-34
[9]   MOLECULAR PROFILE OF REACTIVE ASTROCYTES - IMPLICATIONS FOR THEIR ROLE IN NEUROLOGIC DISEASE [J].
EDDLESTON, M ;
MUCKE, L .
NEUROSCIENCE, 1993, 54 (01) :15-36
[10]   NITRIC-OXIDE SYNTHASE ISOZYMES - CHARACTERIZATION, PURIFICATION, MOLECULAR-CLONING, AND FUNCTIONS [J].
FORSTERMANN, U ;
CLOSS, EI ;
POLLOCK, JS ;
NAKANE, M ;
SCHWARZ, P ;
GATH, I ;
KLEINERT, H .
HYPERTENSION, 1994, 23 (06) :1121-1131