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干扰素-γ使白细胞介素-1诱导的小鼠血管内皮细胞中的粒细胞-巨噬细胞集落刺激因子信使核糖核酸不稳定。

Interferon-gamma destabilizes interleukin-1-induced granulocyte-macrophage colony-stimulating factor mRNA in murine vascular endothelial cells.

作者信息

Akahane K, Pluznik D H

机构信息

Division of Cytokine Biology, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892.

出版信息

Exp Hematol. 1993 Jul;21(7):878-84.

PMID:8319780
Abstract

Vascular endothelial cells can affect hematopoiesis by releasing granulocyte-macrophage colony-stimulating factor (GM-CSF). In the present study, we show that GM-CSF production in murine aorta-derived vascular endothelial cells is regulated by two cytokines:interleukin-1 (IL-1), which induces the production of GM-CSF, and interferon gamma (IFN-gamma), which downregulates this production. The GM-CSF gene is constitutively transcribed in these cells and the transcription rate of the GM-CSF gene does not change with either IL-1 alone or IL-1 plus IFN-gamma. Whereas IL-1 treatment increases the GM-CSF mRNA half-life, simultaneous treatment with IL-1 plus IFN-gamma results in a decrease in the mRNA half-life. IL-1 also enhances IL-6 mRNA accumulation in these cells, although by increasing its transcription rate. In this case, IFN-gamma does not affect IL-6 mRNA expression. These data suggest that IL-1-induced GM-CSF expression in endothelial cells is regulated at the posttranscriptional level and that IFN-gamma specifically inhibits GM-CSF expression via destabilization of the mRNA. These suppressive effects of IFN-gamma provide evidence for an additional role of IFN-gamma in regulating GM-CSF production.

摘要

血管内皮细胞可通过释放粒细胞-巨噬细胞集落刺激因子(GM-CSF)来影响造血作用。在本研究中,我们发现小鼠主动脉来源的血管内皮细胞中GM-CSF的产生受两种细胞因子调节:诱导GM-CSF产生的白细胞介素-1(IL-1)和下调其产生的干扰素γ(IFN-γ)。GM-CSF基因在这些细胞中持续转录,且GM-CSF基因的转录速率不会因单独使用IL-1或IL-1加IFN-γ而改变。虽然IL-1处理会增加GM-CSF mRNA的半衰期,但IL-1与IFN-γ同时处理会导致mRNA半衰期缩短。IL-1还通过提高转录速率增强这些细胞中IL-6 mRNA的积累。在这种情况下,IFN-γ不影响IL-6 mRNA的表达。这些数据表明,内皮细胞中IL-1诱导的GM-CSF表达在转录后水平受到调节,且IFN-γ通过使mRNA不稳定来特异性抑制GM-CSF的表达。IFN-γ的这些抑制作用为IFN-γ在调节GM-CSF产生中的额外作用提供了证据。

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