Prostaglandin E1 protects against liver injury induced by Escherichia coli infection via a dominant Th2-like response of liver T cells in mice

被引:18
作者
Mokuno, Y
Takano, M
Matsuguchi, T
Nishimura, H
Washizu, J
Naiki, Y
Nimura, Y
Yoshikai, Y
机构
[1] Nagoya Univ, Sch Med, Res Inst Dis Mechanism & Control, Lab Host Def & Germfree Life,Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, Sch Med, Dept Surg 1, Nagoya, Aichi 4668550, Japan
关键词
D O I
10.1002/hep.510300606
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Prostaglandin E series (PGEs) are known to protect against lipopolysaccharide (LPS)-induced liver injury by down-regulating the production of inflammatory cytokines. We show here a novel mechanism whereby prostaglandin E-1 protects mice against liver injury after Escherichia coli infection. Prostaglandin E-1 administration suppressed circulating interleukin 12 (IL-12) levels but increased the IL-10 production after E. coli challenge. Furthermore, prostaglandin E-1-alpha-cyclodextrin (PGE(1)) shifted the Th1/Th2 balance of CD3(intermediate) IL-2R beta(+) T cells in the Liver to a dominant Th2-like response. Neutralization of endogenous IL-4 by administration of anti-IL-4 monoclonal antibody (mAb) diminished the inhibitory effect of prostaglandin E-1 on liver injury after E. coli challenge. These results suggested that the Th2-like response of liver T cells may be at least partly involved in the mechanism whereby prostaglandin E-1 protects against E. coli-induced liver injury.
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页码:1464 / 1472
页数:9
相关论文
共 54 条
[1]  
ARAI T, 1995, J IMMUNOL, V155, P5743
[2]  
Barbulescu K, 1998, J IMMUNOL, V160, P3642
[3]   Mouse CD1-specific NK1 T cells: Development, specificity, and function [J].
Bendelac, A ;
Rivera, MN ;
Park, SH ;
Roark, JH .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :535-562
[4]   A SUBSET OF CD4(+) THYMOCYTES SELECTED BY MHC CLASS-I MOLECULES [J].
BENDELAC, A ;
KILLEEN, N ;
LITTMAN, DR ;
SCHWARTZ, RH .
SCIENCE, 1994, 263 (5154) :1774-1778
[5]   GAMMA-INTERFERON - THE MATCH THAT LIGHTS THE FIRE [J].
BILLIAU, A .
IMMUNOLOGY TODAY, 1988, 9 (02) :37-40
[6]   Molecular cloning and characterization of the four rat prostaglandin E2 prostanoid receptor subtypes [J].
Boie, Y ;
Stocco, R ;
Sawyer, N ;
Slipetz, DM ;
Ungrin, MD ;
Neuschäfer-Rube, F ;
Püschel, GP ;
Metters, KM ;
Abramovitz, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1997, 340 (2-3) :227-241
[7]   DEVELOPMENTALLY REGULATED EXPRESSION OF T-CELL RECEPTOR BETA-CHAIN VARIABLE DOMAINS IN IMMATURE THYMOCYTES [J].
BUDD, RC ;
MIESCHER, GC ;
HOWE, RC ;
LEES, RK ;
BRON, C ;
MACDONALD, HR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 166 (02) :577-582
[8]   INTERLEUKIN-2 TRANSCRIPTION FACTORS AS MOLECULAR TARGETS OF CAMP INHIBITION - DELAYED INHIBITION-KINETICS AND COMBINATORIAL TRANSCRIPTION ROLES [J].
CHEN, D ;
ROTHENBERG, EV .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (03) :931-942
[9]   Induction of TH1 and TH2 CD4+ T cell responses: The alternative approaches [J].
Constant, SL ;
Bottomly, K .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :297-322
[10]   Interleukin-4-producing CD4(+) NK1.1(+) TCR alpha/beta(intermediate) liver lymphocytes are downregulated by Listeria monocytogenes [J].
Emoto, M ;
Emoto, Y ;
Kaufmann, SHE .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (12) :3321-3325