26kd膜结合肿瘤坏死因子前体对17kd肿瘤坏死因子(TNF)产生的双向反馈调节。

Journal of inflammation Pub Date : 1995-01-01
I G Soma, T Nishizawa, H Inagawa, Y Tanabe, K Noguchi, S Goto, K Takagi, D Mizuno
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引用次数: 0

摘要

基于26kd膜结合性坏死因子前体(proTNF)可能作为维持成人体内平衡的主要调节因子的假设,我们试图研究proTNF是否在特定细胞反应中表现出双向调节。我们研究了急性单核细胞白血病细胞THP-1在脂多糖刺激下产生17kd成熟TNF。经证实,经LPS刺激的同源细胞(引物THP-1)产生成熟的TNF时,THP-1细胞的ProTNF起到正向调节作用,而当THP-1细胞与表达TNF前的NIH3T3共培养时,LPS显著抑制THP-1产生成熟的TNF。这些结果表明,前TNF确实参与了THP-1细胞自身通过细胞间接触对TNF产生的双向反馈调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bidirectional feedback regulation on 17 kD tumor necrosis factor (TNF) production by 26 kD membrane-bound TNF precursor.

Based on the hypothesis that 26 kD membrane-bound rumor necrosis factor precursor (proTNF) may act as a principle regulator to maintain homeostasis in an adult, we tried to examine whether proTNF shows bidirectional regulation in specific cellular response. We focused on production of 17 kD mature TNF by acute monocytic leukemia cells THP-1 after stimulation by lipopolysaccharide. ProTNF of primed THP-1 cells had been shown to act as a positive regulator for production of mature TNF by homologous cells (primed THP-1) after LPS stimulation, whereas when THP-1 cells were co-cultivated with NIH3T3 which expressed pro-TNF, production of mature TNF by THP-1 by LPS was significantly suppressed. These results suggested that pro-TNF was really involved in bidirectional feedback regulation for TNF production by THP-1 cells themselves through cell to cell contact.

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