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首页> 外文期刊>Molecular and Cellular Biology >Induction of the granulocyte-macrophage colony-stimulating factor (CSF) receptor by granulocyte CSF increases the differentiative options of a murine hematopoietic progenitor cell.
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Induction of the granulocyte-macrophage colony-stimulating factor (CSF) receptor by granulocyte CSF increases the differentiative options of a murine hematopoietic progenitor cell.

机译:粒细胞CSF诱导粒细胞-巨噬细胞集落刺激因子(CSF)受体增加了鼠造血祖细胞的分化选择。

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摘要

32DC13(G) is an interleukin-3-dependent murine hematopoietic precursor cell line which differentiates into neutrophilic granulocytes upon exposure to granulocyte colony-stimulating factor (G-CSF) but ceases to proliferate and dies when exposed to granulocyte-macrophage (GM)-CSF. Surface receptors for GM-CSF are undetectable on 32DC13(G) cells but can be induced by priming the cells with G-CSF. Exposure of the G-CSF-primed cells to GM-CSF then results in the generation of monocytes as well as granulocytes. The acquired competence to respond to GM-CSF remains irreversibly encoded in the primed cells, although the GM-CSF receptor can be down regulated by interleukin-3. This phenomenon suggests a mechanism by which hematopoietic precursors may obtain additional receptors, thereby increasing their differentiative potential.
机译:32DC13(G)是白细胞介素3依赖性的小鼠造血前体细胞系,在暴露于粒细胞集落刺激因子(G-CSF)时可分化为嗜中性粒细胞,但在暴露于粒细胞巨噬细胞(GM)-时会停止增殖并死亡脑脊液。 GM-CSF的表面受体在32DC13(G)细胞上无法检测到,但可以通过用G-CSF引发细胞来诱导。然后,将G-CSF引发的细胞暴露于GM-CSF,导致单核细胞以及粒细胞的产生。尽管GM-CSF受体可以被白介素3下调,但获得的对GM-CSF的反应能力仍不可逆转地编码在初免细胞中。这种现象表明造血前体可通过该机制获得其他受体,从而增加其分化潜能。

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