RETINOIC ACID-INDUCED GROWTH-INHIBITION OF A HUMAN MYELOMA CELL-LINE VIA DOWN-REGULATION OF IL-6 RECEPTORS

被引:0
作者
SIDELL, N
TAGA, T
HIRANO, T
KISHIMOTO, T
SAXON, A
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,BRAIN RES INST,DEPT MED,DIV CLIN IMMUNOL ALLERGY,LOS ANGELES,CA 90024
[2] UNIV CALIF LOS ANGELES,SCH MED,JONSSON COMPREHENS CANC CTR,LOS ANGELES,CA 90024
[3] OSAKA UNIV,DIV IMMUNOL,SUITA,OSAKA 565,JAPAN
[4] HIROSHIMA UNIV,DEPT INTERNAL MED,HIROSHIMA 735,JAPAN
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this report we demonstrate that retinoic acid (RA) down-regulated the number of IL-6R on human leukocyte cell lines, including the myeloma cell line AF10, and two B cell hybridomas that correspond to cells at earlier stages of B cell development. Using AF10 cells, whose growth was determined to be mediated by the autocrine action of IL-6, we found that RA reduction of IL-6R was concentration-dependent over a range of 10(-11) to 10(-5) M and corresponded to the ability of the retinoid to inhibit cell proliferation. The down-regulation of IL-6R number by RA was accompanied by reduced IL-6R mRNA expression. RA did not affect endogeneous IL-6 synthesis or secretion from AF10 cells. However, addition of exogenous rIL-6 could overcome RA-induced growth inhibition. Menthol, a structurally unrelated compound to RA, also suppressed IL-6R expression and, correspondingly, inhibited cell growth. Taken together, our results suggest that the antiproliferative action of RA on AF10 cells is caused by reduction of IL-6R expression and subsequent inhibition of IL-6-mediated autocrine growth. These findings suggest the possibility that down-regulation of IL-6R is a means by which RA can modulate immune function.
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页码:3809 / 3814
页数:6
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