Interaction between enteric epithelial cells and Peyer's patch lymphocytes in response to Shigella lipopolysaccharide:: Effect on nitric oxide and IL-6 release

被引:10
作者
Jie Chen
Chuen-Pei Ng
Dewi K Rowlands
Peng-Hui Xu
Jie-Ying Gao
Yiu-Wa Chung
Hsiao-Chang Chan [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Physiol, Fac Med, Epithelial Cell Biol Res Ctr, Shatin, Hong Kong, Peoples R China
[2] Acad Mil Med Sci, Inst Microbiol & Epidemiol, Dept Immunol, Beijing 100071, Peoples R China
[3] Shanxi Med Univ, Fac Med, Dept Biol, Taiyuan 030001, Shanxi Province, Peoples R China
关键词
Shigella F2a-12 LPS; colon epithelial cells (Caco-2); Peyer's patch lymphocyte; coculture; nitric oxide; interleukin-6; LAMINA PROPRIA FIBROBLASTS; IGA SECRETION; UP-REGULATION; BARRIER; SYNTHASE; MODULATION; INOS; INTERLEUKIN-6; ENTEROCYTE; EXPRESSION;
D O I
10.3748/wjg.v12.i24.3895
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: To investigate the effect of interaction between enteric epithelial cells and lymphocytes of Peyer's patch on the release of nitric oxide (NO) and IL-6 in response to Shigella lipopolysaccharide (LPS). Methods: Human colonic epithelial cells (Caco-2) were mixed cocultured with lymphocytes of Peyer's patch from wild-type (C57 mice) and inducible NO synthase knockout mice, and challenged with Shigella F2a-12 LPS. Release of NO and mIL-6 was measured by Griess colorimetric assay and enzyme-linked immunosorbent assay (ELISA), respectively. Results: In the absence of LPS challenge, NO was detected in the culture medium of Caco-2 epithelial cells but not in lymphocytes of Peyer's patch, and the NO release was further up-regulated in both cocultures with lymphocytes from either the wild-type or NOS knockout mice, with a significantly higher level observed in the coculture with NOS knockout lymphocytes. After Shigella F2a-12 LPS challenge for 24-h, NO production was significantly increased in both Caco-2 alone and the coculture with lymphocytes of Peyer's patch from the wild-type mice but not from NOS knockout mice. LPS was found to stimulate the release of mIL-6 from lymphocytes, which was suppressed by coculture with Caco-2 epithelial cells. The LPS-induced mIL-6 production in lymphocytes from NOS knockout mice was significantly greater than that from the wild-type mice. Conclusion: Lymphocytes of Peyer's patch maintain a constitutive basal level of NO production from the enteric epithelial cell Caco-2. LPS-incluced mIL-6 release from lymphocytes of Peyer's patch is suppressed by the cocultured epithelial cells. While no changes are detectable in NO production in lymphocytes from both wild-type and NOS knockout mice before and after LPS challenge, NO from lymphocytes appears to play an inhibitory role in epithelial NO release and their own mIL-6 release in response to LPS. (C) 2006 The WJG Press. All rights reserved.
引用
收藏
页码:3895 / 3900
页数:6
相关论文
共 37 条
[11]   The two faces of IL-6 on Th1/Th2 differentiation [J].
Diehl, S ;
Rincón, M .
MOLECULAR IMMUNOLOGY, 2002, 39 (09) :531-536
[12]   Lipopolysaccharide-induced enterocyte-derived nitric oxide induces intestinal monolayer permeability in an autocrine fashion [J].
Forsythe, RM ;
Xu, DZ ;
Lu, Q ;
Deitch, EA .
SHOCK, 2002, 17 (03) :180-184
[13]   HUMAN APPENDIX B-CELLS NATURALLY EXPRESS RECEPTORS FOR AND RESPOND TO INTERLEUKIN-6 WITH SELECTIVE IGA1 AND IGA2 SYNTHESIS [J].
FUJIHASHI, K ;
MCGHEE, JR ;
LUE, C ;
BEAGLEY, KW ;
TAGA, T ;
HIRANO, T ;
KISHIMOTO, T ;
MESTECKY, J ;
KIYONO, H .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (01) :248-252
[14]   Preferential enhancement of B cell IgA secretion by intestinal epithelial cell-derived cytokines and interleukin-2 [J].
Goodrich, ME ;
McGee, DW .
IMMUNOLOGICAL INVESTIGATIONS, 1999, 28 (01) :67-75
[15]   Regulation of mucosal B cell immunoglobulin secretion by intestinal epithelial cell-derived cytokines [J].
Goodrich, ME ;
McGee, DW .
CYTOKINE, 1998, 10 (12) :948-955
[16]   Inducible nitric oxide synthase mediates early epithelial repair of porcine ileum [J].
Gookin, JL ;
Rhoads, JM ;
Argenzio, RA .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2002, 283 (01) :G157-G168
[17]   Interaction of microorganisms, epithelium, and lymphoid cells of the mucosa-associated lymphoid tissue [J].
Hamzaoui, N ;
Pringault, E .
INTESTINAL PLASTICITY IN HEALTH AND DISEASE, 1998, 859 :65-74
[18]   Intraepithelial lymphocytes coinduce nitric oxide synthase in intestinal epithelial cells [J].
Hoffman, RA .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2000, 278 (06) :G886-G894
[19]   Upregulation of iNOS by COX-2 in muscularis resident macrophage of rat intestine stimulated with LPS [J].
Hori, M ;
Kita, M ;
Torihashi, S ;
Miyamoto, S ;
Won, KJ ;
Sato, K ;
Ozaki, H ;
Karaki, H .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2001, 280 (05) :G930-G938
[20]   In situ characterization of inflammatory responses in the rectal mucosae of patients with shigellosis [J].
Islam, D ;
Veress, B ;
Bardhan, PK ;
Lindberg, AA ;
Christensson, B .
INFECTION AND IMMUNITY, 1997, 65 (02) :739-749