Probiotics and commensals reverse TNF-α- and IFN-γ-induced dysfunction in human intestinal epithelial cells

被引:237
作者
Resta-Lenert, S [1 ]
Barrett, KE [1 ]
机构
[1] Univ Calif San Diego, Med Ctr 8414, Sch Med, Dept Med, San Diego, CA 92103 USA
关键词
D O I
10.1053/j.gastro.2005.12.015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Commensal bacteria are crucial for the development of the mucosal immune system. Probiotics are commensals with special characteristics and may protect mucosal surfaces against pathogens. Pathogens cause significant phenotypic alterations in infected epithelial cells, and probiotics reverse these deleterious responses. We hypothesized that probiotics and/or commensals may also reverse epithelial damage produced by cytokines. Methods: Human intestinal epithelial cells were exposed basolaterally to interferon (IFN)-gamma (10(3) U/mL) or tumor necrosis factor (TNF)-alpha (10 ng/mL) for up to 48 hours and assessed for ion transport, transepithelial resistance (TER), and epithelial permeability in the presence or absence of probiotics (Streptococcus thermophilus [ST] and Lactobacillus acidophilus [LA]), or the commensal, Bacteroides thetaiotaomicron (BT). Results: Agonist-stimulated chloride secretion was inhibited by IFN-gamma, an effect prevented by ST/LA or BT. The ability of ST/LA or BT to restore Cl- secretion was blocked by inhibitors of p38 MAPK, ERK1, 2, and PI3K. The cystic fibrosis transmembrane conductance regulator (CFTR) and the NKCC1 cotransporter were down-regulated by IFN-gamma, and ST/LA pretreatment reversed this effect. Both TNF-alpha and IFN-gamma significantly reduced TER and increased epithelial permeability, effects prevented by ST/LA or BT. A Janus kinase (JAK) inhibitor synergistically potentiated effects of ST/LA or BT on TER and permeability, but p38, ERK1, 2, or PI3K inhibition did not. Finally, only probiotic-treated epithelial cells exposed to cytokines showed reduced activation of SOCS3 and STAT1,3. Conclusions: Deleterious effects of TNF-alpha and IFN-gamma on epithelial function are prevented by probiotic, and to a lesser extent, commensal pretreatment. These data extend the spectrum of effects of such bacteria on intestinal epithelial function and may justify their use in inflammatory disorders.
引用
收藏
页码:731 / 746
页数:16
相关论文
共 52 条
[1]  
ADAMS RB, 1993, J IMMUNOL, V150, P2356
[2]   Future therapies for inflammatory bowel disease [J].
Stephen J. Bickston ;
Lawrence W. Comerford ;
Fabio Cominelli .
Current Gastroenterology Reports, 2003, 5 (6) :518-523
[3]   IL-1β and TNF-α, but not IFN-α, IFN-γ, IL-6 or IL-8, are secretory mediators in human distal colon [J].
Bode, H ;
Schmitz, H ;
Fromm, M ;
Scholz, P ;
Riecken, EO ;
Schulzke, JD .
CYTOKINE, 1998, 10 (06) :457-465
[4]   Toll-like receptor 2 enhances ZO-1-associated intestinal epithelial barrier integrity via protein kinase C [J].
Cario, E ;
Gerken, G ;
Podolsky, DK .
GASTROENTEROLOGY, 2004, 127 (01) :224-238
[5]   Enterohemorrhagic Escherichia coli O157:H7 disrupts Stat1-mediated gamma interferon signal transduction in epithelial cells [J].
Ceponis, PJM ;
McKay, DM ;
Ching, JCY ;
Pereira, P ;
Sherman, PM .
INFECTION AND IMMUNITY, 2003, 71 (03) :1396-1404
[6]   Glutamine deprivation facilitates tumour necrosis factor induced bacterial translocation in Caco-2 cells by depletion of enterocyte fuel substrate [J].
Clark, EC ;
Patel, SD ;
Chadwick, PR ;
Warhurst, G ;
Curry, A ;
Carlson, GL .
GUT, 2003, 52 (02) :224-+
[7]  
Cummings J H, 2003, Curr Issues Intest Microbiol, V4, P9
[8]   Synergistic effects of interferon γ and tumour necrosis factor α on T84 cell function [J].
Fish, SM ;
Proujansky, R ;
Reenstra, WW .
GUT, 1999, 45 (02) :191-198
[9]   INTRODUCTION OF PAM-BETA-1 INTO LISTERIA-MONOCYTOGENES BY CONJUGATION AND HOMOLOGY BETWEEN NATIVE L-MONOCYTOGENES PLASMIDS [J].
FLAMM, RK ;
HINRICHS, DJ ;
THOMASHOW, MF .
INFECTION AND IMMUNITY, 1984, 44 (01) :157-161
[10]   Analysis of SOCS-3 promoter responses to interferon γ [J].
Gatto, L ;
Berlato, C ;
Poli, V ;
Tininini, S ;
Kinjyo, I ;
Yoshimura, A ;
Cassatella, MA ;
Bazzoni, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (14) :13746-13754