MECHANISMS OF DIFFERENTIAL REGULATION OF INTERLEUKIN-6 MESSENGER-RNA ACCUMULATION BY TUMOR NECROSIS FACTOR-ALPHA AND LYMPHOTOXIN DURING MONOCYTIC DIFFERENTIATION

被引:28
作者
BRACH, MA
CICCO, NA
RIEDEL, D
HIRANO, T
KISHIMOTO, T
MERTELSMANN, RH
HERRMANN, F
机构
[1] UNIV FREIBURG,DEPT INTERNAL MED 1,W-7800 FREIBURG,GERMANY
[2] OSAKA UNIV,INST MOLEC & CELLULAR BIOL,OSAKA,JAPAN
关键词
Gene expression; Interleukin-6; Lymphotoxin; Tumor necrosis factor;
D O I
10.1016/0014-5793(90)81411-G
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the present report we compare the capacity of two related cytokines, tumor necrosis factor (TNF) alpha and lymphotoxin (LT), to modulate mRNA levels of interleukin-6 (IL-6) in cells representing different stages of monocytic differentiation including the human leukemia cell lines HL 60, U 937, THP-1, MonoMac 1 and peripheral blood monocytes. We show that the capacity of TNF alpha and LT to induce IL-6 mRNA accumulation increases as monocytic differentiation proceeds with TNF alpha being more potent than LT, suggesting that alternate pathways may be used by differentiating cells to control expression of IL-6. In contrast, in monocytes which constitutively synthesize IL-6 transcripts, TNF alpha and LT treatment had opposite effects on levels of IL-6 mRNA accumulation. In these cells TNF alpha enhanced steady state levels of IL-6 transcripts due to mRNA stabilization, whereas LT shortened IL-6 mRNA half-life, most likely due to induction of a RNA destabilizer since LT-mediated downregulation of levels of IL-6 mRNA in monocytes could be prevented by inhibition of protein synthesis. Neither TNF alpha nor LT altered IL-6 mRNA accumulation by interfering with preexisting transcription factors since both TNF alpha and LT required de novo protein synthesis to exert their effects. © 1990.
引用
收藏
页码:349 / 354
页数:6
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