Expression of heme oxygenase and inducible nitric oxide synthase mRNA in human brain tumors

被引:106
作者
Hara, E
Takahashi, K
Tominaga, T
Kumabe, T
Kayama, T
Suzuki, H
Fujita, H
Yoshimoto, T
Shirato, K
Shibahara, S
机构
[1] TOHOKU UNIV, DEPT APPL PHYSIOL & MOLEC BIOL, SCH MED, AOBA KU, SENDAI, MIYAGI 98077, JAPAN
[2] TOHOKU UNIV, DEPT NEUROSURG, SCH MED, AOBA KU, SENDAI, MIYAGI 98077, JAPAN
[3] TOHOKU UNIV, DEPT INTERNAL MED 1, SCH MED, AOBA KU, SENDAI, MIYAGI 98077, JAPAN
关键词
D O I
10.1006/bbrc.1996.0999
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
Heme oxygenase-1, a key enzyme in heme catabolism, and inducible nitric oxide synthase (iNOS) are responsible for production of carbon monoxide and nitric oxide (NO), respectively. Expression of each enzyme has been shown to be modulated by heme and NO, raising a possibility for the coordinated regulation of the two enzymes. We therefore analyzed the expression levels of both mRNA in humans using brain tumors. Either heme oxygenase-l or iNOS mRNA was expressed at higher levels in brain tumors compared to the brain tissue, but their expression levels were not apparently correlated. Tn the brain tumor cell lines, treatment with cytokines increased the expression of iNOS mRNA but not heme oxygenase 1 mRNA, whereas treatment with an NO donor increased the expression of heme oxygenase-l mRNA but not MOS mRNA. These results suggest the separate regulation of expression of both enzyme mRNA in humans. (C) 1996 Academic Press, Inc.
引用
收藏
页码:153 / 158
页数:6
相关论文
共 44 条
[1]   Intracellular assembly of inducible NO synthase is limited by nitric oxide-mediated changes in heme insertion and availability [J].
Albakri, QA ;
Stuehr, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (10) :5414-5421
[2]  
BAEK KJ, 1993, J BIOL CHEM, V268, P21120
[3]   NITRIC-OXIDE GENERATION FROM NITROPRUSSIDE BY VASCULAR TISSUE - EVIDENCE THAT REDUCTION OF THE NITROPRUSSIDE ANION AND CYANIDE LOSS ARE REQUIRED [J].
BATES, JN ;
BAKER, MT ;
GUERRA, R ;
HARRISON, DG .
BIOCHEMICAL PHARMACOLOGY, 1991, 42 :S157-S165
[4]   EVIDENCE FOR THE INVOLVEMENT OF HIPPOCAMPAL CO PRODUCTION IN THE ACQUISITION AND CONSOLIDATION OF INHIBITORY AVOIDANCE-LEARNING [J].
BERNABEU, R ;
PRINC, F ;
DESTEIN, ML ;
FIN, C ;
JUKNAT, AA ;
BATILE, A ;
IZQUIERDO, I ;
MEDINA, JH .
NEUROREPORT, 1995, 6 (03) :516-518
[5]   MODULATION OF CARBON-MONOXIDE PRODUCTION AND ENHANCED SPATIAL-LEARNING BY TIN PROTOPORPHYRIN [J].
BING, O ;
GRUNDEMAR, L ;
NY, L ;
MOLLER, C ;
HEILIG, M .
NEUROREPORT, 1995, 6 (10) :1369-1372
[6]   INDUCTION OF NITRIC-OXIDE SYNTHASE IN DEMYELINATING REGIONS OF MULTIPLE-SCLEROSIS BRAINS [J].
BO, L ;
DAWSON, TM ;
WESSELINGH, S ;
MORK, S ;
CHOI, S ;
KONG, PA ;
HANLEY, D ;
TRAPP, BD .
ANNALS OF NEUROLOGY, 1994, 36 (05) :778-786
[7]   INDUCTION OF NITRIC-OXIDE SYNTHASE MESSENGER-RNA EXPRESSION - SUPPRESSION BY EXOGENOUS NITRIC-OXIDE [J].
COLASANTI, M ;
PERSICHINI, T ;
MENEGAZZI, M ;
MARIOTTO, S ;
GIORDANO, E ;
CALDARERA, CM ;
SOGOS, V ;
LAURO, GM ;
SUZUKI, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :26731-26733
[8]   A NOVEL NEURONAL MESSENGER MOLECULE IN BRAIN - THE FREE-RADICAL, NITRIC-OXIDE [J].
DAWSON, TM ;
DAWSON, VL ;
SNYDER, SH .
ANNALS OF NEUROLOGY, 1992, 32 (03) :297-311
[9]   Transcriptional regulation of human inducible nitric oxide synthase (NOS2) gene by cytokines: Initial analysis of the human NOS2 promoter [J].
deVera, ME ;
Shapiro, RA ;
Nussler, AK ;
Mudgett, JS ;
Simmons, RL ;
Morris, SM ;
Billiar, TR ;
Geller, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (03) :1054-1059
[10]   NITRIC-OXIDE AND THE CEREBRAL-CIRCULATION [J].
FARACI, FM ;
BRIAN, JE .
STROKE, 1994, 25 (03) :692-703