TRANSFORMING GROWTH-FACTOR-BETA DIFFERENTIALLY MODULATES THE INDUCIBLE NITRIC-OXIDE SYNTHASE GENE IN DISTINCT CELL-TYPES

被引:73
作者
GILBERT, RS [1 ]
HERSCHMAN, HR [1 ]
机构
[1] UNIV CALIF LOS ANGELES, SCH MED, BIOMED & ENVIRONM SCI LAB, LOS ANGELES, CA 90024 USA
关键词
D O I
10.1006/bbrc.1993.2054
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
Nitric oxide is a mediator of paracrine cell signalling. An inducible form of nitric oxide synthase (iNOS) is expressed in macrophages and in Swiss 3T3 cells. Transforming growth factor beta (TGF-beta) is a cytokine that modulates many cellular functions. We find that TGF-beta cannot induce iNOS mRNA expression, either in macrophage cell lines or in Swiss 3T3 cells. However, TGF-beta attenuates lipopolysaccharide induction of iNOS mRNA in macrophages. In contrast, TGF-beta enhances iNOS induction by phorbol ester, serum or lipopolysaccharide in 3T3 cells. Thus TGF-beta can inhibit or augment iNOS mRNA induction in response to primary inducers, depending on the cell type in question. © 1993 Academic Press. All rights reserved.
引用
收藏
页码:380 / 384
页数:5
相关论文
共 37 条
[1]   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
[2]  
Curtis-Prior P. B., 1988, PROSTAGLANDINS BIOL
[3]   A COLLECTION OF MESSENGER-RNA SPECIES THAT ARE INDUCIBLE IN THE RAW-264.7 MOUSE MACROPHAGE CELL-LINE BY GAMMA INTERFERON AND OTHER AGENTS [J].
FARBER, JM .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (04) :1535-1545
[4]  
FLETCHER BS, 1992, J BIOL CHEM, V267, P4338
[5]   CYTOKINES, ENDOTOXIN, AND GLUCOCORTICOIDS REGULATE THE EXPRESSION OF INDUCIBLE NITRIC-OXIDE SYNTHASE IN HEPATOCYTES [J].
GELLER, DA ;
NUSSLER, AK ;
DISILVIO, M ;
LOWENSTEIN, CJ ;
SHAPIRO, RA ;
WANG, SC ;
SIMMONS, RL ;
BILLIAR, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :522-526
[6]  
GILBERT RP, UNPUB
[7]   HUMAN CYCLOOXYGENASE-2 CDNA [J].
HLA, T ;
NEILSON, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (16) :7384-7388
[8]  
JANSSENS SP, 1992, J BIOL CHEM, V267, P14519
[9]  
KITAGAWA T, 1991, J BIOL CHEM, V266, P18066
[10]  
KUJUBU DA, 1991, J BIOL CHEM, V266, P12866