Oxidants, transcription factors, and intestinal inflammation

被引:25
作者
Jourd'heuil, D [1 ]
Morise, Z [1 ]
Conner, EM [1 ]
Grisham, MB [1 ]
机构
[1] Louisiana State Univ, Med Ctr, Dept Mol & Cellular Physiol, Shreveport, LA 71130 USA
关键词
reactive oxygen metabolites; nitric oxide; nuclear transcription factor kappa B; activator protein 1; B-cell lymphoma/leukemia-2;
D O I
10.1097/00004836-199700001-00011
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
It is now well appreciated that chronic gut inflammation is characterized by enhanced production of reactive metabolites of oxygen and nitrogen. Some of these oxidants are known to modulate the expression of a variety of genes that are involved in the immune and inflammatory responses. For example, certain oxidants are known to activate the nuclear transcription factor kappa B, which regulates the expression of a variety of different adhesion molecules, cytokines, and enzymes. Oxidants are also known to activate another transcription factor, activator protein-1. This transcription factor is composed of products from the fos and jun proto-oncogene family and is believed to be important in regulating cell growth and proliferation. Finally, oxidants are believed to promote intestinal epithelial cell apoptosis, and the B-cell lymphoma/leukemia-2 gene product is believed to inhibit this phenomenon in an antioxidant-dependent manner. Taken together, these observations suggest that nontoxic concentrations of reactive metabolites of oxygen and nitrogen play an important role in regulating the expression of genes involved in the inflammatory response and in modulating apoptosis.
引用
收藏
页码:S61 / S72
页数:12
相关论文
共 116 条
[1]   REDOX REGULATION OF FOS AND JUN DNA-BINDING ACTIVITY INVITRO [J].
ABATE, C ;
PATEL, L ;
RAUSCHER, FJ ;
CURRAN, T .
SCIENCE, 1990, 249 (4973) :1157-1161
[2]   OXIDATIVE STRESS INDUCES NF-KAPPA-B DNA-BINDING AND INDUCIBLE NOS MESSENGER-RNA IN HUMAN EPITHELIAL-CELLS [J].
ADCOCK, IM ;
BROWN, CR ;
KWON, O ;
BARNES, PJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 199 (03) :1518-1524
[3]   CLINICAL-EVIDENCE SUPPORTING THE RADICAL SCAVENGER MECHANISM OF 5-AMINOSALICYLIC ACID [J].
AHNFELTRONNE, I ;
NIELSEN, OH ;
CHRISTENSEN, A ;
LANGHOLZ, E ;
BINDER, V ;
RIIS, P .
GASTROENTEROLOGY, 1990, 98 (05) :1162-1169
[4]  
AIKENS J, 1991, J BIOL CHEM, V266, P15091
[5]   SPONTANEOUS INTESTINAL INFLAMMATION AND NITRIC-OXIDE METABOLISM IN HLA-B27 TRANSGENIC RATS [J].
AIKO, S ;
GRISHAM, MB .
GASTROENTEROLOGY, 1995, 109 (01) :142-150
[6]  
AIKO S, 1995, GASTROENTEROLOGY, V108, pA268
[7]   SEPARATION OF OXIDANT-INITIATED AND REDOX-REGULATED STEPS IN THE NF-KAPPA-B SIGNAL-TRANSDUCTION PATHWAY [J].
ANDERSON, MT ;
STAAL, FJT ;
GITLER, C ;
HERZENBERG, LA ;
HERZENBERG, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (24) :11527-11531
[8]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[9]  
BAEUERLE PA, 1994, ANNU REV IMMUNOL, V12, P141, DOI 10.1146/annurev.immunol.12.1.141
[10]  
BAEUERLE PA, 1995, SCIENCE, V268, P522