首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Upregulation of Interleukin 6 and Granulocyte Colony-Stimulating Factor Receptors by Transcription Factor CCAAT Enhancer Binding Protein α (C/EBPα) Is Critical for Granulopoiesis
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Upregulation of Interleukin 6 and Granulocyte Colony-Stimulating Factor Receptors by Transcription Factor CCAAT Enhancer Binding Protein α (C/EBPα) Is Critical for Granulopoiesis

机译:转录因子CCAAT增强剂结合蛋白α(C /EBPα)对白细胞介素6和粒细胞集落刺激因子受体的上调对于粒细胞生成至关重要

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摘要

Cytokines stimulate granulopoiesis through signaling via receptors whose expression is controlled by lineage-specific transcription factors. Previously, we demonstrated that granulocyte colony-stimulating factor (G-CSF) receptor mRNA was undetectable and granulocyte maturation blocked in CCAAT enhancer binding protein α (C/EBPα)-deficient mice. This phenotype is distinct from that of G-CSF receptor−/− mice, suggesting that other genes are likely to be adversely affected by loss of C/EBPα. Here we demonstrate loss of interleukin 6 (IL-6) receptor and IL-6–responsive colony-forming units (CFU-IL6) in C/EBPα−/− mice. The observed failure of granulopoiesis could be rescued by the addition of soluble IL-6 receptor and IL-6 or by retroviral transduction of G-CSF receptors, demonstrating that loss of both of these receptors contributes to the absolute block in granulocyte maturation observed in C/EBPα-deficient hematopoietic cells. The results of these and other studies suggest that additional C/EBPα target genes, possibly other cytokine receptors, are also important for the block in granulocyte differentiation observed in vivo in C/EBPα-deficient mice.
机译:细胞因子通过受体的信号传导来刺激粒细胞生成,其表达受谱系特异性转录因子控制。以前,我们证明了在CCAAT增强子结合蛋白α(C /EBPα)缺陷小鼠中无法检测到粒细胞集落刺激因子(G-CSF)受体mRNA,并且粒细胞成熟受到阻滞。此表型与G-CSF受体-/-小鼠不同,表明其他基因可能受到C /EBPα丢失的不利影响。在这里,我们证明了C /EBPα-/-小鼠中白介素6(IL-6)受体和IL-6应答菌落形成单位(CFU-IL6)的丢失。可以通过添加可溶性IL-6受体和IL-6或通过逆转录病毒转导G-CSF受体来挽救观察到的粒细胞生成失败,这表明这两种受体的丧失都有助于C中观察到的粒细胞成熟的绝对阻断/EBPα缺陷的造血细胞。这些研究和其他研究的结果表明,其他C /EBPα靶基因,可能还有其他细胞因子受体,对于C /EBPα缺陷小鼠体内观察到的粒细胞分化阻滞也很重要。

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