Intraepithelial lymphocytes coinduce nitric oxide synthase in intestinal epithelial cells

被引:17
作者
Hoffman, RA [1 ]
机构
[1] Univ Pittsburgh, Dept Surg, Pittsburgh, PA 15261 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2000年 / 278卷 / 06期
关键词
cell-cell interaction; intestine; inflammation;
D O I
10.1152/ajpgi.2000.278.6.G886
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The study of mucosal immunity has revealed that complex reciprocal interactions occur between intestinal intraepithelial lymphocytes (IEL) and intestinal epithelial cells (IEC). The present study focuses on the induction of inducible nitric oxide (NO) synthase in cocultures of freshly isolated rat IEL and the rat epithelial cell line IEC-18 after the addition of interleukin-1 beta (IL-1 beta), tumor necrosis factor-alpha, or lipopolysaccharide. When IEL and IEC were separated using Transwell chambers, NO synthesis was not induced, indicating that cell-cell contact was required. Culture of IEC-18 with IEL, even in the absence of inflammatory stimuli such as IL-1 beta, resulted in upregulation of class I and II antigens on IEC-18, due to the interferon-gamma (IFN-gamma) that is constitutively produced by IEL. Addition of anti-IFN-gamma antibody to the NO-producing cocultures resulted in inhibition of NO synthesis as well as the upregulation of class I and II antigen expression. These data indicate that IFN-gamma production by IEL conditions IEC for the expression of other components of the inflammatory process.
引用
收藏
页码:G886 / G894
页数:9
相关论文
共 35 条
[21]   Functional expression of costimulatory molecule CD88 on epithelial cells in the inflamed colonic mucose [J].
Nakazawa, A ;
Watanabe, M ;
Kanai, T ;
Yajima, T ;
Yamazaki, M ;
Ogata, H ;
Ishii, H ;
Azuma, M ;
Hibi, T .
GASTROENTEROLOGY, 1999, 117 (03) :536-545
[22]   A critical role for transforming growth factor-beta but not interleukin 4 in the suppression of T helper type 1-mediated colitis by CD45RB(low) CD4(+) T cells [J].
Powrie, F ;
Carlino, J ;
Leach, MW ;
Mauze, S ;
Coffman, RL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (06) :2669-2674
[23]   EPITHELIOID CELL-CULTURES FROM RAT SMALL-INTESTINE - CHARACTERIZATION BY MORPHOLOGIC AND IMMUNOLOGICAL CRITERIA [J].
QUARONI, A ;
WANDS, J ;
TRELSTAD, RL ;
ISSELBACHER, KJ .
JOURNAL OF CELL BIOLOGY, 1979, 80 (02) :248-265
[24]   ULCERATIVE COLITIS-LIKE DISEASE IN MICE WITH A DISRUPTED INTERLEUKIN-2 GENE [J].
SADLACK, B ;
MERZ, H ;
SCHORLE, H ;
SCHIMPL, A ;
FELLER, AC ;
HORAK, I .
CELL, 1993, 75 (02) :253-261
[25]   WIDESPREAD TISSUE DISTRIBUTION, SPECIES DISTRIBUTION AND CHANGES IN ACTIVITY OF CA2+-DEPENDENT AND CA2+-INDEPENDENT NITRIC-OXIDE SYNTHASES [J].
SALTER, M ;
KNOWLES, RG ;
MONCADA, S .
FEBS LETTERS, 1991, 291 (01) :145-149
[26]   Expression of inducible nitric oxide synthase and nitrotyrosine in colonic epithelium in inflammatory bowel disease [J].
Singer, II ;
Kawka, DW ;
Scott, S ;
Weidner, JR ;
Mumford, RA ;
Riehl, TE ;
Stenson, WF .
GASTROENTEROLOGY, 1996, 111 (04) :871-885
[27]  
STEINIGER B, 1989, IMMUNOLOGY, V68, P507
[28]   T-CELL-MEDIATED COGNATE SIGNALING OF NITRIC-OXIDE PRODUCTION BY MACROPHAGES - REQUIREMENTS FOR MACROPHAGE ACTIVATION BY PLASMA-MEMBRANES ISOLATED FROM T-CELLS [J].
TAO, X ;
STOUT, RD .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (11) :2916-2921
[29]   ACTIVATED T-CELLS ENHANCE NITRIC-OXIDE PRODUCTION BY MURINE SPLENIC MACROPHAGES THROUGH GP39 AND LFA-1 [J].
TIAN, LC ;
NOELLE, RJ ;
LAWRENCE, DA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (01) :306-309
[30]   A new isolation method for rat intraepithelial lymphocytes [J].
Todd, D ;
Singh, AJ ;
Greiner, DL ;
Mordes, JP ;
Rossini, AA ;
Bortell, R .
JOURNAL OF IMMUNOLOGICAL METHODS, 1999, 224 (1-2) :111-127