In vivo alterations of IFN regulatory factor-1 and PIAS1 protein levels in cystic fibrosis epithelium

被引:46
作者
Kelley, TJ [1 ]
Elmer, HL [1 ]
机构
[1] Case Western Reserve Univ, Dept Pediat, Cleveland, OH 44106 USA
关键词
D O I
10.1172/JCI9560
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Inducible nitric oxide synthase-2 (NOS2) expression has been shown to be reduced in cystic fibrosis (CF) epithelial cells. Reduced NOS2 expression is unexpected, given the inflammatory nature of CF airway disease, and is an indication that cell-signaling mechanisms necessary for proper NOS2 regulation are probably altered in CF epithelium. Therefore, we examined the expression levels of regulatory factors necessary for NOS2 expression in CF epithelium and showed that IFN regulatory factor-1 (IRF-1) is necessary for full NOS2 expression, Mice lacking IRF-1 expression have diminished epithelial NOS2 expression, as well as reduced NO-dependent chloride transport across the nasal epithelia. Furthermore, IRF-1 protein expression is reduced in nasal and intestinal epithelial cells from CF mice, suggesting a possible mechanism for the CF related reduction of epithelial NOS2 expression. Active signal transducer and activator of transcription-1 (Stat1) is necessary for both NOS2 and IRF-1 expression. We found that protein levels of Stat1 were increased in CF cells, but that the active phosphorylated form of Stat1 was bound to the protein inhibitor of activated Stat1 (PIAS1). We propose that increased levels of PIAS1 diminish certain cell-signaling pathways, resulting in reduced IRF-1 and NOS2 expression in CF epithelial cells.
引用
收藏
页码:403 / 410
页数:8
相关论文
共 33 条
[1]   Overproduction of the CFTR R domain leads to increased levels of AsialoGM1 and increased Pseudomonas aeruginosa binding by epithelial cells [J].
Bryan, R ;
Kube, D ;
Perez, A ;
Davis, P ;
Prince, A .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 19 (02) :269-277
[2]   Analysis of the cytokine-stimulated human inducible nitric oxide synthase (iNOS) gene: Characterization of differences between human and mouse iNOS promoters [J].
Chu, SC ;
Marks-Konczalik, J ;
Wu, HP ;
Banks, TC ;
Moss, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 248 (03) :871-878
[3]   DIETARY-CHANGES IMPROVE SURVIVAL OF CFTR S489X HOMOZYGOUS MUTANT MOUSE [J].
ECKMAN, EA ;
COTTON, CU ;
KUBE, DM ;
DAVIS, PB .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1995, 269 (05) :L625-L630
[4]   Nitric oxide-mediated regulation of transepithelial sodium and chloride transport in murine nasal epithelium [J].
Elmer, HL ;
Brady, KG ;
Drumm, ML ;
Kelley, TJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1999, 276 (03) :L466-L473
[5]   Attenuation of nitric oxide synthase induction in IRF-1-deficient glial cells [J].
Fujimura, M ;
Tominaga, T ;
Kato, I ;
Takasawa, S ;
Kawase, M ;
Taniguchi, T ;
Okamoto, H ;
Yoshimoto, T .
BRAIN RESEARCH, 1997, 759 (02) :247-250
[6]   An interferon-gamma-activated site (GAS) is necessary for full expression of the mouse iNOS gene in response to interferon-gamma and lipopolysaccharide [J].
Gao, JJ ;
Morrison, DC ;
Parmely, TJ ;
Russell, SW ;
Murphy, WJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (02) :1226-1230
[7]   HYPERABSORPTION OF NA+ AND RAISED CA2+-MEDIATED CL- SECRETION IN NASAL EPITHELIA OF CF MICE [J].
GRUBB, BR ;
VICK, RN ;
BOUCHER, RC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (05) :C1478-C1483
[8]   Interferon gamma and interleukin 4 stimulate prolonged expression of inducible nitric oxide synthase in human airway epithelium through synthesis of soluble mediators [J].
Guo, FH ;
Uetani, K ;
Haque, SJ ;
Williams, BRG ;
Dweik, RA ;
Thunnissen, FBJM ;
Calhoun, W ;
Erzurum, SC .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (04) :829-838
[9]   Prolonged STAT1 activation is associated with interferon-γ priming for interleukin-1-induced inducible nitric-oxide synthase expression by islets of Langerhans [J].
Heitmeier, MR ;
Scarim, AL ;
Corbett, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (41) :29266-29273
[10]   ORGAN SPECIFIC CYTOKINE THERAPY - LOCAL ACTIVATION OF MONONUCLEAR PHAGOCYTES BY DELIVERY OF AN AEROSOL OF RECOMBINANT INTERFERON-GAMMA TO THE HUMAN LUNG [J].
JAFFE, HA ;
BUHL, R ;
MASTRANGELI, A ;
HOLROYD, KJ ;
SALTINI, C ;
CZERSKI, D ;
JAFFE, HS ;
KRAMER, S ;
SHERWIN, S ;
CRYSTAL, RG .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (01) :297-302