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Tumor necrosis factor alpha directly and indirectly regulates hematopoietic progenitor cell proliferation: role of colony-stimulating factor receptor modulation

机译:肿瘤坏死因子α直接和间接调节造血祖细胞增殖:集落刺激因子受体调节的作用

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摘要

Tumor necrosis factor alpha (TNF-alpha) has been shown to both stimulate and inhibit the proliferation of hematopoietic progenitor cells (HPCs) in vitro, but its mechanisms of action are not known. We demonstrate that the direct effects of TNF-alpha on murine bone marrow progenitors are only inhibitory and mediated at least in part through downmodulation of colony-stimulating factor receptor (CSF-R) expression. The stimulatory effects of TNF-alpha are indirectly mediated through production of hematopoietic growth factors, which subsequently results in increased granulocyte-macrophage CSF and interleukin 3 receptor expression. In addition, the effects of TNF- alpha (stimulatory or inhibitory) are strictly dependent on the particular CSF stimulating growth as well as the concentration of TNF- alpha present in culture. A model is proposed to explain how TNF-alpha might directly and indirectly regulate HPC growth through modulation of CSF-R expression.
机译:肿瘤坏死因子α(TNF-alpha)已显示出在体外刺激和抑制造血祖细胞(HPC)的增殖,但其作用机理尚不清楚。我们证明,TNF-α对鼠类骨髓祖细胞的直接作用仅是抑制性的,至少是通过下调集落刺激因子受体(CSF-R)的表达而介导的。 TNF-α的刺激作用通过造血生长因子的产生间接介导,随后导致粒细胞巨噬细胞CSF和白介素3受体表达增加。另外,TNF-α的作用(刺激性或抑制性)严格取决于特定的CSF刺激生长以及培养物中存在的TNF-α的浓度。提出了一个模型来解释TNF-α如何通过调节CSF-R表达来直接和间接调节HPC的生长。

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