AUTOCRINE REGULATION OF ICAM-1 EXPRESSION ON BLADDER-CANCER CELL-LINES - EVIDENCE FOR THE ROLE OF IL-1-ALPHA

被引:27
作者
ALEXANDROFF, AB [1 ]
JACKSON, AM [1 ]
ESUVARANATHAN, K [1 ]
PRESCOTT, S [1 ]
JAMES, K [1 ]
机构
[1] RUSSIA PAEDIAT HAEMATOL RES INST,MOSCOW,RUSSIA
关键词
INTERCELLULAR ADHESION MOLECULE-1; ADHESION MOLECULE; CYTOKINE; BLADDER CANCER; INTERLEUKIN-1-ALPHA; AUTOCRINE PRODUCTION;
D O I
10.1016/0165-2478(94)90182-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have studied the autocrine regulation of essential expression of the intercellular adhesion molecule-1 (ICAM-1) on 8 transitional cell carcinoma (TCC) cell lines (histopathological grades 1-3). The constitutive expression of ICAM-1 was regulated by soluble factors in an autocrine fashion. These factors were produced by all cell lines, with the exception of the MGH-U1 cell line. The effects observed could be largely attributed to IL-1 alpha. However, the residual ICAM-1 inducing activity (up to 30% of ICAM-1 induction) could not be associated with any known ICAM-1 inducers (IFN gamma, TNF alpha, TNF beta, IL-1 alpha, IL-1 beta, IL-4, retinoic acid, LPS). In contrast to recombinant derived cytokines, the IL-alpha present in tissue culture supernatant was only able to induce ICAM-1 on high-grade tumours and not low-grade cells. This discriminative effect is similar to that noted following in vitro culture of tumour cells with bacillus Calmette-Guerin organisms. Whether the production of soluble factors (e.g., IL-1 alpha) by TCC cell lines plays an essential autocrine role for bladder tumours and/or affects the interaction with cells of the immune system needs to be investigated further.
引用
收藏
页码:117 / 124
页数:8
相关论文
共 24 条
[1]  
APTE RN, 1994, IMMUNOL LETT, V39, P45
[2]   CYTOKINES - COORDINATORS OF IMMUNE AND INFLAMMATORY RESPONSES [J].
ARAI, K ;
LEE, F ;
MIYAJIMA, A ;
MIYATAKE, S ;
ARAI, N ;
YOKOTA, T .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :783-836
[3]  
BACUS SS, 1993, CANCER RES, V53, P5251
[4]   REGULATION BY RETINOIC ACID OF ICAM-1 EXPRESSION ON HUMAN TUMOR-CELL LINES [J].
BOUILLON, M ;
TESSIER, P ;
BOULIANNE, R ;
DESTREMPE, R ;
AUDETTE, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1097 (02) :95-102
[5]   PURIFICATION, CLONING, EXPRESSION AND BIOLOGICAL CHARACTERIZATION OF AN INTERLEUKIN-1 RECEPTOR ANTAGONIST PROTEIN [J].
CARTER, DB ;
DEIBEL, MR ;
DUNN, CJ ;
TOMICH, CSC ;
LABORDE, AL ;
SLIGHTOM, JL ;
BERGER, AE ;
BIENKOWSKI, MJ ;
SUN, FF ;
MCEWAN, RN ;
HARRIS, PKW ;
YEM, AW ;
WASZAK, GA ;
CHOSAY, JG ;
SIEU, LC ;
HARDEE, MM ;
ZURCHERNEELY, HA ;
REARDON, IM ;
HEINRIKSON, RL ;
TRUESDELL, SE ;
SHELLY, JA ;
EESSALU, TE ;
TAYLOR, BM ;
TRACEY, DE .
NATURE, 1990, 344 (6267) :633-638
[6]  
COSIMI AB, 1990, J IMMUNOL, V144, P4604
[7]   COSTIMULATION VIA VASCULAR CELL-ADHESION MOLECULE-1 INDUCES IN T-CELLS INCREASED RESPONSIVENESS TO THE CD28 COUNTER-RECEPTOR-B7 [J].
DAMLE, NK ;
KLUSSMAN, K ;
LEYTZE, G ;
OCHS, HD ;
ARUFFO, A ;
LINSLEY, PS ;
LEDBETTER, JA .
CELLULAR IMMUNOLOGY, 1993, 148 (01) :144-156
[8]  
DUSTIN ML, 1986, J IMMUNOL, V137, P245
[9]  
Esuvaranathan Kesavan, 1993, Journal of Urology, V149, p271A
[10]   A MONOCLONAL-ANTIBODY DIRECTED AGAINST THE HUMAN INTERCELLULAR-ADHESION MOLECULE (ICAM-1) MODULATES THE RELEASE OF TUMOR-NECROSIS-FACTOR-ALPHA, INTERFERON-GAMMA AND INTERLEUKIN-1 [J].
GEISSLER, D ;
GAGGL, S ;
MOST, J ;
GREIL, R ;
HEROLD, M ;
DIERICH, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (12) :2591-2596