Selective regulation of intercellular adhesion molecule-1 expression by interleukin-18 and interleukin-12 on human monocytes

被引:51
作者
Stuyt, RJL
Netea, MG
Geijtenbeek, TBH
Kullberg, BJ
Dinarello, CA
van der Meer, JWM
机构
[1] Radboud Univ Nijmegen Med Ctr, Dept Med 541, NL-6500 HB Nijmegen, Netherlands
[2] Univ Nijmegen, Ctr Infect Dis, Nijmegen, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr Amsterdam, Dept Mol Cell Biol, Amsterdam, Netherlands
[4] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80262 USA
关键词
D O I
10.1046/j.1365-2567.2003.01747.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Induction of expression of adhesion molecules is a crucial step in inflammation. The role of interleukin-18 (IL-18) in induction of various adhesion molecules was investigated in freshly isolated peripheral blood mononuclear cells and human monocyte and T-cell lines. IL-18 selectively up-regulated intercellular adhesion molecule-1 (ICAM-1) expression on freshly isolated human monocytes, but not on lymphocytes. The expression of other adhesion molecules was not influenced. Induction of ICAM-1 by IL-18 was dependent on endogenous tumour necrosis factor-alpha (TNF-alpha), and IL-12 had an additive effect on that of IL-18. No changes in adhesion molecule expression were observed on the monocytic cell line THP-1 and on the T-cell lines HSB-2 and Jurkat J16. In addition, induction of ICAM-1 on monocytes by lipopolysaccharide was slightly, but significantly, inhibited by blockade of either endogenous IL-18 or TNF-alpha with IL-18 binding protein or TNF binding protein, respectively. Blocking IL-1 effects with IL-1 receptor antagonist did not influence ICAM-1 levels. In conclusion, IL-18 selectively up-regulates the expression of ICAM-1 on monocytes, and this contributes to the proinflammatory effects of this cytokine.
引用
收藏
页码:329 / 334
页数:6
相关论文
共 37 条
[1]   KIM185, A MONOCLONAL-ANTIBODY TO CD18 WHICH INDUCES A CHANGE IN THE CONFORMATION OF CD18 AND PROMOTES BOTH LFA-1-DEPENDENT AND CR3-DEPENDENT ADHESION [J].
ANDREW, D ;
SHOCK, A ;
BALL, E ;
ORTLEPP, S ;
BELL, J ;
ROBINSON, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (09) :2217-2222
[2]   Expression of lung vascular and airway ICAM-1 after exposure to bacterial lipopolysaccharide [J].
BeckSchimmer, B ;
Schimmer, RC ;
Warner, RL ;
Schmal, H ;
Nordblom, G ;
Flory, CM ;
Lesch, ME ;
Friedl, HP ;
Schrier, DJ ;
Ward, PA .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 17 (03) :344-352
[3]   DISTINCT BINDING OF T-LYMPHOCYTES TO ICAM-1, ICAM-2 OR ICAM-3 UPON ACTIVATION OF LFA-1 [J].
BINNERTS, ME ;
VANKOOYK, Y ;
SIMMONS, DL ;
FIGDOR, CG .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (09) :2155-2160
[4]  
CALIGARISCAPPIO F, 1985, BLOOD, V66, P1035
[5]  
CARLOS TM, 1994, BLOOD, V84, P2068
[6]   CHARACTERIZATION OF ICAM-2 AND EVIDENCE FOR A 3RD COUNTER-RECEPTOR FOR LFA-1 [J].
DEFOUGEROLLES, AR ;
STACKER, SA ;
SCHWARTING, R ;
SPRINGER, TA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (01) :253-267
[7]   ICAM-1 (CD54) - A COUNTER-RECEPTOR FOR MAC-1 (CD11B CD18) [J].
DIAMOND, MS ;
STAUNTON, DE ;
DEFOUGEROLLES, AR ;
STACKER, SA ;
GARCIAAGUILAR, J ;
HIBBS, ML ;
SPRINGER, TA .
JOURNAL OF CELL BIOLOGY, 1990, 111 (06) :3129-3139
[8]   Overview of interleukin-18:: more than an interferon-γ inducing factor [J].
Dinarello, CA ;
Novick, D ;
Puren, AJ ;
Fantuzzi, G ;
Shapiro, L ;
Mühl, H ;
Yoon, DY ;
Reznikov, LL ;
Kim, SH ;
Rubinstein, M .
JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 63 (06) :658-664
[9]   ENDURANCE RUN INCREASES CIRCULATING IL-6 AND IL-1RA BUT DOWN-REGULATES EX-VIVO TNF-ALPHA AND IL-1-BETA PRODUCTION [J].
DRENTH, JPH ;
VANUUM, SHM ;
VANDEUREN, M ;
PESMAN, GJ ;
VANDERVENJONGEKRIJG, J ;
VANDERMEER, JWM .
JOURNAL OF APPLIED PHYSIOLOGY, 1995, 79 (05) :1497-1503
[10]  
DUSTIN ML, 1986, J IMMUNOL, V137, P245