Low environmental pH is responsible for the induction of nitric-oxide synthase in macrophages -: Evidence for involvement of nuclear factor-κB activation

被引:183
作者
Bellocq, A
Suberville, S
Philippe, C
Bertrand, F
Perez, J
Fouqueray, B
Cherqui, G
Baud, L
机构
[1] Hop Tenon, INSERM, U64, F-75020 Paris, France
[2] Hop St Antoine, INSERM, U402, F-75012 Paris, France
关键词
D O I
10.1074/jbc.273.9.5086
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
Stimulation of macrophages with endotoxin and/or cytokines is responsible for the expression of the inducible isoform of nitric oxide synthase (MOS). Because macrophages are exposed to low pH within the microenvironment of inflammatory lesions, the potential role of acidic pH as an additional regulator of iNOS was investigated, Substitution of the culture medium of rat peritoneal macrophages at pH 7.4 with medium at pH 7.0 up-regulated iNOS activity, as reflected by a 2.5-fold increase in nitrite accumulation, The increase in iNOS activity was associated with a similar increase in iNOS mRNA expression that reflected an increase in iNOS mRNA synthesis rather than stability, Low environmental pH-induced iNOS gene transcription involved the activation of nuclear factor-kappa B (NF-kappa B) transcription factor since exposure of macrophages to low environmental pH both increased NF-kappa B binding activity in the nucleus and enhanced NF-kappa B-driven reporter gene expression, In addition, treatment of macrophages with pyrrolidine dithiocarbamate or n-acetyl-leucinyl-leucinyl-norleucinal, two drugs preventing NF-kappa B translocation to the nucleus, canceled low pH-induced nitrite accumulation, The overall mechanism required the synthesis of tumor necrosis factor alpha (TNF alpha). Indeed, 1) elevated TNF alpha bioactivity was observed in the medium of macrophages exposed to pH 7.0, and 2) incubation of macrophages with a neutralizing anti-TNF alpha antibody impaired both NF-kappa B activation and nitrite accumulation in response to acid challenge, In summary, exposure of macrophages to acidic microenvironment in inflammatory lesions leads to the up-regulation of iNOS activity through the activation of NF-kappa B.
引用
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页码:5086 / 5092
页数:7
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共 38 条
[1]  
ALARD P, 1993, BIOTECHNIQUES, V15, P730
[2]   The acidosis of chronic renal failure activates muscle proteolysis in rats by augmenting transcription of genes encoding proteins of the ATP-dependent ubiquitin-proteasome pathway [J].
Bailey, JL ;
Wang, XN ;
England, BK ;
Price, SR ;
Ding, XY ;
Mitch, WE .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (06) :1447-1453
[3]   LEUKOTRIENE-D4-INDUCED INCREASES IN THE CYTOPLASMIC PH OF HUMAN MYELOCYTIC LEUKOCYTES [J].
BAUD, L ;
HEALY, A ;
CRAGOE, EJ ;
GOETZL, EJ ;
KOO, CH .
JOURNAL OF CELLULAR PHYSIOLOGY, 1988, 136 (02) :355-360
[4]   LEUKOTRIENE-D4-INDUCED PROLIFERATION OF GLOMERULAR EPITHELIAL-CELLS - PKC-MEDIATED AND NA+-H+ EXCHANGER-MEDIATED RESPONSE [J].
BAUD, L ;
PEREZ, J ;
CHERQUI, G ;
CRAGOE, EJ ;
ARDAILLOU, R .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (02) :C232-C239
[5]   DISCRIMINATION BETWEEN CITRULLINE AND ARGININE TRANSPORT IN ACTIVATED MURINE MACROPHAGES - INEFFICIENT SYNTHESIS OF NO FROM RECYCLING OF CITRULLINE TO ARGININE [J].
BAYDOUN, AR ;
BOGLE, RG ;
PEARSON, JD ;
MANN, GE .
BRITISH JOURNAL OF PHARMACOLOGY, 1994, 112 (02) :487-492
[6]   INSULIN ACTIVATES NUCLEAR FACTOR KAPPA-B IN MAMMALIAN-CELLS THROUGH A RAF-1-MEDIATED PATHWAY [J].
BERTRAND, F ;
PHILIPPE, C ;
ANTOINE, PJ ;
BAUD, L ;
GROYER, A ;
CAPEAU, J ;
CHERQUI, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (41) :24435-24441
[7]  
BOUTARD V, 1995, J IMMUNOL, V155, P2077
[8]   BETA-LACTAMASE ACTIVITY IN HUMAN PUS [J].
BRYANT, RE ;
RASHAD, AL ;
MAZZA, JA ;
HAMMOND, D .
JOURNAL OF INFECTIOUS DISEASES, 1980, 142 (04) :594-601
[9]   REGULATION OF INDUCIBLE NITRIC-OXIDE SYNTHASE MESSENGER-RNA LEVELS BY LPS, INF-GAMMA, TGF-BETA, AND IL-10 IN MURINE MACROPHAGE CELL-LINES AND RAT PERITONEAL-MACROPHAGES [J].
CHESROWN, SE ;
MONNIER, J ;
VISNER, G ;
NICK, HS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 200 (01) :126-134
[10]   IDENTIFICATION AND ANALYSIS OF ALL COMPONENTS OF A GEL RETARDATION ASSAY BY COMBINATION WITH IMMUNOBLOTTING [J].
DEMCZUK, S ;
HARBERS, M ;
VENNSTROM, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2574-2578