The heat shock response inhibits inducible nitric oxide synthase gene expression by blocking I kappa-B degradation and NF-kappa B nuclear translocation

被引:110
作者
Wong, HR [1 ]
Ryan, M [1 ]
Wispe, JR [1 ]
机构
[1] CHILDRENS HOSP, MED CTR, DIV PULM BIOL, CINCINNATI, OH 45229 USA
关键词
D O I
10.1006/bbrc.1997.6076
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
We investigated the mechanisms by which the heat shock response inhibits inducible nitric oxide synthase (iNOS) gene expression. Incubation of cultured murine lung epithelium (MLE-15) at temperatures ranging from 39 to 43 degrees C, for 1 h, demonstrated that only severe thermal stress (41 to 43 degrees C) was sufficient to induce the heat shock response. Thermal stress inhibited cytokine-mediated iNOS gene expression only when associated with induction of the heat shock response. Transient transfection assays with an iNOS promoter-reporter gene construct demonstrated that the heat shock response inhibited cytokine-mediated iNOS promoter activity. Electromobility gel shift assays demonstrated that the heat shock response inhibited cytokine-mediated NF-kappa B nuclear translocation. The heat shock response also inhibited cytokine-mediated I kappa-B degradation. These data suggest that the heat shock response inhibits iNOS gene expression by transcriptional mechanisms involving the NF-kappa B/I kappa-B pathway. (C) 1997 Academic Press.
引用
收藏
页码:257 / 263
页数:7
相关论文
共 31 条
[1]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[2]  
Cahill CM, 1996, J BIOL CHEM, V271, P24874
[3]   Cytokine-induced nitric oxide synthase gene transcription is blocked by the heat shock response in human liver cells [J].
deVera, ME ;
Wong, JM ;
Zhou, JY ;
Tzeng, E ;
Wong, HR ;
Billiar, TR ;
Geller, DA .
SURGERY, 1996, 120 (02) :144-149
[4]   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
[5]   WARMING MACROPHAGES TO FEBRILE RANGE DESTABILIZES TUMOR-NECROSIS-FACTOR-ALPHA MESSENGER-RNA WITHOUT INDUCING HEAT-SHOCK [J].
ENSOR, JE ;
CRAWFORD, EK ;
HASDAY, JD .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 269 (05) :C1140-C1146
[6]   Heat shock protein 70 suppresses astroglial-inducible nitric-oxide synthase expression by decreasing NF kappa B activation [J].
Feinstein, DL ;
Galea, E ;
Aquino, DA ;
Li, GC ;
Xu, H ;
Reis, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (30) :17724-17732
[7]  
GOLDENBERG CJ, 1988, J BIOL CHEM, V263, P19734
[8]   HSP induction inhibits iNOS mRNA expression and attenuates hypotension in endotoxin-challenged rats [J].
Hauser, GJ ;
Dayao, EK ;
Wasserloos, K ;
Pitt, BR ;
Wong, HR .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 271 (06) :H2529-H2535
[9]   HYPERTHERMIA PROTECTS MICE AGAINST THE LETHAL EFFECTS OF ENDOTOXIN [J].
HOTCHKISS, R ;
NUNNALLY, I ;
LINDQUIST, S ;
TAULIEN, J ;
PERDRIZET, G ;
KARL, I .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (06) :R1447-R1457
[10]   MAJOR HEAT-SHOCK PROTEIN HSP70 PROTECTS TUMOR-CELLS FROM TUMOR-NECROSIS-FACTOR CYTOTOXICITY [J].
JAATTELA, M ;
WISSING, D ;
BAUER, PA ;
LI, GC .
EMBO JOURNAL, 1992, 11 (10) :3507-3512