Regulation of human 12/15-lipoxygenase by stat6-dependent transcription

被引:48
作者
Conrad, DJ
Lu, M
机构
[1] VA San Diego Healthcare Syst, Sect Pulm & Crit Care, San Diego, CA 92161 USA
[2] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA
[3] Vet Med Res Fdn, San Diego, CA USA
关键词
D O I
10.1165/ajrcmb.22.2.3786
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
Human 12/15-lipoxygenase is a lipid-peroxidating enzyme implicated in the pathophysiology of atherosclerosis and airway inflammation. Interleukin (IL)-4 specifically induces 12/15-lipoxygenase messenger RNA. protein. and enzymatic activity in primary cultures of human monocytes and airway epithelial cells. The induction of the human 12/15-lipoxygenase by IL-4 suggests that the signal transducer and activator of transcription (Stat)-6 protein is critical for its expression. Several putative Stat6 response elements are located in the proximal 1.8 kb of 12/15-lipoxygenase 5'-flanking region. In this study we use BEAS-2B human airway epithelial cells as a model to demonstrate the dependence of 12/15-lipoxygenase expression on the IL-4/Stat6 signal transduction pathway. Transient transfections of human 12/15-lipoxygenase promoter/luciferase reporter genes indicate that this induction occurs through direct transcriptional mechanisms mediated by a specific Stat6 response element located 952 base pairs upstream of the translational start codon, Using this Stat6 response element as a probe. electrophoretic mobility shift assays show an IL-4-dependent binding activity in nuclear extracts. Supershift assays, confirm that Stat6 participates in this binding complex. These data indicate that the human 12/15-lipoxygenase gene is induced in airway epithelial cells through Stat6-dependent transcriptional mechanisms mediated by a specific Stat6 response element in the 5'-flanking region.
引用
收藏
页码:226 / 234
页数:9
相关论文
共 51 条
[1]   Abrogation of bronchial eosinophilic inflammation and airway hyperreactivity in signal transducers and activators of transcription (STAT)6-deficient mice [J].
Akimoto, T ;
Numata, F ;
Tamura, M ;
Takata, Y ;
Higashida, N ;
Takashi, T ;
Takeda, K ;
Akira, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (09) :1537-1542
[2]   ENHANCED LEVELS OF LIPOPEROXIDES IN LOW-DENSITY-LIPOPROTEIN INCUBATED WITH MURINE FIBROBLASTS EXPRESSING HIGH-LEVELS OF HUMAN 15-LIPOXYGENASE [J].
BENZ, DJ ;
MOL, M ;
EZAKI, M ;
MORIITO, N ;
ZELAN, I ;
MIYANOHARA, A ;
FRIEDMANN, T ;
PARTHASARATHY, S ;
STEINBERG, D ;
WITZTUM, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (10) :5191-5197
[3]   Discovery of a second 15S-lipoxygenase in humans [J].
Brash, AR ;
Boeglin, WE ;
Chang, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (12) :6148-6152
[4]   Regulation of 15-lipoxygenase expression in lung epithelial cells by interleukin-4 [J].
Brinckmann, R ;
Topp, MS ;
Zalan, I ;
Heydeck, D ;
Ludwig, P ;
Kuhn, H ;
Berdel, WE ;
Habenicht, AJR .
BIOCHEMICAL JOURNAL, 1996, 318 :305-312
[5]  
CHEN XS, 1994, J BIOL CHEM, V269, P13979
[6]   SPECIFIC INFLAMMATORY CYTOKINES REGULATE THE EXPRESSION OF HUMAN MONOCYTE 15-LIPOXYGENASE [J].
CONRAD, DJ ;
KUHN, H ;
MULKINS, M ;
HIGHLAND, E ;
SIGAL, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (01) :217-221
[7]   LIPOXIN FORMATION IN HUMAN NASAL POLYPS AND BRONCHIAL TISSUE [J].
EDENIUS, C ;
KUMLIN, M ;
BJORK, T ;
ANGGARD, A ;
LINDGREN, JA .
FEBS LETTERS, 1990, 272 (1-2) :25-28
[8]   Altered responses of human macrophages to lipopolysaccharide by hydroperoxy eicosatetraenoic acid, hydroxy eicosatetraenoic acid, and arachidonic acid - Inhibition of tumor necrosis factor production [J].
Ferrante, JV ;
Huang, ZH ;
Nandoskar, M ;
Hii, CST ;
Robinson, BS ;
Rathjen, DA ;
Poulos, A ;
Morris, CP ;
Ferrante, A .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (06) :1445-1452
[9]   THE COMPLETE SEQUENCE OF THE RABBIT ERYTHROID CELL-SPECIFIC 15-LIPOXYGENASE MESSENGER-RNA - COMPARISON OF THE PREDICTED AMINO-ACID SEQUENCE OF THE ERYTHROCYTE LIPOXYGENASE WITH OTHER LIPOXYGENASES [J].
FLEMING, J ;
THIELE, BJ ;
CHESTER, J ;
OPREY, J ;
JANETZKI, S ;
AITKEN, A ;
ANTON, IA ;
RAPOPORT, SM ;
HARRISON, PR .
GENE, 1989, 79 (01) :181-188
[10]   Hypolipidemic drugs, polyunsaturated fatty acids, and eicosanoids are ligands for peroxisome proliferator-activated receptors alpha and delta [J].
Forman, BM ;
Chen, J ;
Evans, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) :4312-4317