Enterocytes are the primary source of the chemokine ENA-78 in normal colon and ulcerative colitis

被引:82
作者
Keates, S
Keates, AC
Mizoguchi, E
Bhan, A
Kelly, CP
机构
[1] HARVARD UNIV, BETH ISRAEL DEACONESS MED CTR, SCH MED, DIV GASTROENTEROL, BOSTON, MA 02215 USA
[2] HARVARD UNIV, MASSACHUSETTS GEN HOSP, SCH MED, IMMUNOPATHOL DEPT, BOSTON, MA 02215 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1997年 / 273卷 / 01期
关键词
inflammatory bowel disease; interleukin-8; chemotaxis; inflammation;
D O I
10.1152/ajpgi.1997.273.1.G75
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Epithelial cell-derived neutrophil-activating protein-78 (ENA-78) is a neutrophil-directed C-X-C chemokine. We report that Caco-2 and T84 human intestinal epithelial cells produce ENA-78 after stimulation by interleukin (IL)-1 beta or tumor necrosis factor-alpha. Caco-2 cells show increased IL-8 production at 4-12 h and increased ENA-78 production at 8-24 h after cytokine stimulation. Immunohistochemical studies in normal human colon and in ulcerative colitis demonstrate ENA-78 immunoreactivity principally associated with crypt epithelial cells. Furthermore, human colonic tissues from patients with ulcerative colitis show elevated levels of ENA-78 mRNA (24-fold increase, P < 0.01) and protein (4-fold increase, P < 0.05) compared with normal controls. Thus ENA-78 is produced in normal colon and in ulcerative colitis and is predominantly of enterocyte origin. The kinetics of ENA-78 induction in human colon epithelial cell lines are delayed and prolonged compared with IL-8. We propose that ENA-78 and IL-8 serve complementary and sequential roles in neutrophil recruitment in ulcerative colitis. ENA-78 as an enterocyte-derived, neutrophil-activating chemokine may be especially important in neutrophil recruitment from the lamina propria into the epithelial layer.
引用
收藏
页码:G75 / G82
页数:8
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